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PMC:5118433 / 22203-22209 JSONTXT
Age-Related Differences in the Luminal and Mucosa-Associated Gut Microbiome of Broiler Chickens and Shifts Associated with Campylobacter jejuni Infection
Abstract
Despite the importance of gut microbiota for broiler performance and health little is known about the composition of this ecosystem, its development and response towards bacterial infections. Therefore, the current study was conducted to address the composition and structure of the microbial community in broiler chickens in a longitudinal study from day 1 to day 28 of age in the gut content and on the mucosa. Additionally, the consequences of a Campylobacter (C.) jejuni infection on the microbial community were assessed. The composition of the gut microbiota was analyzed with 16S rRNA gene targeted Illumina MiSeq sequencing. Sequencing of 130 samples yielded 51,825,306 quality-controlled sequences, which clustered into 8285 operational taxonomic units (OTUs; 0.03 distance level) representing 24 phyla. Firmicutes, Proteobacteria, Bacteroidetes, Actinobacteria, and Tenericutes were the main components of the gut microbiota, with Proteobacteria and Firmicutes being the most abundant phyla (between 95.0 and 99.7% of all sequences) at all gut sites. Microbial communities changed in an age-dependent manner. Whereas, young birds had more Proteobacteria, Firmicutes, and Tenericutes dominated in older birds (>14 days old). In addition, 28 day old birds had more diverse bacterial communities than young birds. Furthermore, numerous significant differences in microbial profiles between the mucosa and luminal content of the small and large intestine were detected, with some species being strongly associated with the mucosa whereas others remained within the luminal content of the gut. Following oral infection of 14 day old broiler chickens with 1 × 108 CFU of C. jejuni NCTC 12744, it was found that C. jejuni heavily colonized throughout the small and large intestine. Moreover, C. jejuni colonization was associated with an alteration of the gut microbiota with infected birds having a significantly lower abundance of Escherichia (E.) coli at different gut sites. On the contrary, the level of Clostridium spp. was higher in infected birds compared with birds from the negative controls. In conclusion, the obtained results demonstrate how the bacterial microbiome composition changed within the early life of broiler chickens in the gut lumen and on the mucosal surface. Furthermore, our findings confirmed that the Campylobacter carrier state in chicken is characterized by multiple changes in the intestinal ecology within the host.
Introduction
A diverse microbiota is found throughout the gastrointestinal tract (GIT) of chickens, most predominant in the cecum (Mead, 1997; Videnska et al., 2014). The gut microbiota plays an essential role in nutrition, detoxification of certain compounds, growth performance and protection against pathogenic bacteria. The microbiota is crucial to strengthen the immune system, thereby affecting growth, health, and wellbeing of chicken. Generally, the gut microbiota modulates host responses to limit the colonization of pathogens (Rehman et al., 2007). There is little information about the diversity and function of the gut microbiota in chickens, its impact on the host and the impact of certain pathogens.
Development of the gut microbiota in chickens occurs immediately after hatching and is influenced by both genetic and external factors like diet and environment (Apajalahti et al., 2004). It was reported that disturbances in the intestinal microbiota leads to a delay in growth, weakens the host resistance and increases the susceptibility to various infectious diseases (Lan et al., 2004). Gong et al. (2002) demonstrated that the cecal microbiota protects chickens against bacterial infections, while microbiota in the small intestine contributes significantly to its function, including digestion and nutrient absorption, which significantly determines the growth rate of the bird. Studies on gut microbiota have mostly been performed with chickens older than 1 week of age due to the various influences in day-old birds. However, the composition of gut microbiota at the first day of life in newly hatched chickens is a matter of interest within a longitudinal study. Therefore, the focus of the actual study was to determine the diversity and community structures of the microbiota within the small and large intestine from hatch until 4 weeks of age. Furthermore, differences among the mucosa-associated and luminal content microbiota were determined for the first time.
Campylobacter (C.) jejuni is the most common cause of food-borne bacterial enteritis worldwide (EFSA, 2011). C. jejuni infection of chickens had previously not been considered to influence bird health and it was thought that C. jejuni is part of the normal microbiota of birds (EFSA, 2011). Understanding how Campylobacter species, especially C. jejuni, establishes successful colonization in chickens remains a foremost research priority as this gastrointestinal pathogen not only overcomes the host's defense system, but also competes with the microbial community for space and nutrients.
It has been shown that Campylobacter requires numerous factors to successfully colonize the host, to translocate and to avoid clearance (Awad et al., 2014, 2015a,b, 2016; Humphrey et al., 2014). In addition, Awad et al. (2016) showed that Campylobacter had the ability to reduce butyrate, isobutyrate, valerate, and isovalerate which might be due to the utilization of short-chain fatty acids (SCFAs) as a carbon source (Masanta et al., 2013) or due to the reduction of butyric acid producing bacteria amongst the microbiota. In general, there is a complex interplay between microbiota composition and SCFAs concentration and it was found that the type and level of SCFAs in the gut can affect different members of the microbial community in various ways (Mon et al., 2015).
It is still unknown how C. jejuni affects the ecology of the chicken gut, a feature of high importance considering a possible detrimental effect on the health of birds associated with C. jejuni colonization. Haag et al. (2012) demonstrated that C. jejuni colonization in mice depends on the microbiota of the host and vice versa and Campylobacter colonization induces a shift of the intestinal microbiota. Thus, it can be hypothesized that Campylobacter colonization is associated with an alteration in the intestinal microbiota of chickens as well. Therefore, the second aim of the actual study was to investigate the dynamics of an experimental Campylobacter jejuni NCTC 12744 infection in 14–28 days old chickens and the consequences on the alteration of the gut microbiome.
Materials and methods
Ethics statement
The animal experiment was approved by the institutional ethics committee of the University of Veterinary Medicine and the Ministry of Research and Science under the license number GZ 68.205/0011-11/3b/2013. All husbandry practices were performed with full consideration of animal welfare.
Experimental design
In this study, a total of 45 1-day-old broiler chickens (males and females) were obtained from a commercial hatchery (Ross-308, Geflügelhof Schulz, Graz, Austria). Five day-old birds were immediately sacrificed for determining the gut microbiota of the jejunal and cecal mucosa. At 7 and 14 days of age, five birds were randomly selected for measuring the development of gut microbiota from gut content and mucosa. The birds were kept as non-infected for the first 2 weeks and were housed on wood shavings with feed and water supplied ad libitum. The birds were fed a standard commercial diet for the whole experimental period in order to avoid an influence of the change of diet on the microbial composition.
At the first and 14 days of age birds were confirmed as Campylobacter-free by taking cloacal swabs which were streaked onto modified charcoal-cefaprazone-deoxycholate agar (CM0739, OXOID, Hampshire, UK) and grown for 48 h under microaerophilic conditions at 42°C. At 14 days of age, 15 birds were infected with Campylobacter jejuni (C. jejuni) reference strain NCTC 12744 and kept separately from 15 non-infected control birds which were inoculated with PBS only. C. jejuni was routinely grown in Lennox L Base broth (LB broth) (Invitrogen, California, USA) at 42°C for 48 h in a shaking incubator. Campylobacter colony-forming unit (CFU) was determined from each suspension by serial dilutions in duplicate using LB agar. Campylobacter suspensions were stored at −80°C by adding 2 mL of 40% glycerol/10 mL LB broth. For infection, Campylobacter suspensions were centrifuged for 5 min at 10,000 × rpm. The pellet was washed 3 times with phosphate-buffered saline (PBS) each time centrifuged at the same conditions as mentioned above. Finally, the pellets were resuspended in PBS and the necessary concentration was adjusted for birds' infection.
The infection was performed orally via feeding tube (gavage) with a dose of 1 × 108 CFU/bird at 14 days of age as described previously (Awad et al., 2015a). At 7 days post infection 5 birds from each group were anesthetized by injection of a single dose of thiopental (20 mg/kg) into the wing vein and slaughtered by bleeding of the jugular vein. The final 10 birds/group were killed at 14 days post infection. At each time point the gastrointestinal content from the jejunum and ceca, as well as jejunal and cecal mucosa from 5 birds/group were taken to determine the gut microbiota. Intestinal segments were disclosed at the mesentery with sterile instruments and the digesta was removed. The luminal site of the intestinal segments was washed with sterile ice-cold PBS until the mucosa was completely cleaned from the digesta. The mucosa was rinsed several times with sterile ice cold PBS, after which the mucosa was collected aseptically by scraping off the mucosa using scalpel blades. All samples were stored at −80°C until further processing.
DNA extraction, PCR amplification of the 16S rRNA gene, and illumina MISeq sequencing
DNA from luminal content and gut mucosa samples was extracted using the PowerSoil® DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA, USA) as described previously (Mann et al., 2014; Yasuda et al., 2015). The same protocol of DNA extraction was applied to luminal content and gut mucosa. From each of the 130 samples a total of 250 mg of gut content or mucosa was used for DNA isolation according to manufacturer's instructions. DNA concentration was determined by a Qubit fluorometer (Invitrogen, Carlsbad, CA, USA). The V345 hypervariable region of the 16S rRNA genes was amplified with the primers F341 (5′-GTGYCAGCMGCCGCGGTAA-3′) (Zakrzewski et al., 2012) and R909 (5′-CCGYCAATTYMTTTRAGTTT-3′) (Tamaki et al., 2011). An amplicon size of approximately 568 bp was produced.
16S rRNA gene PCRs, library preparation and sequencing were performed by Microsynth (Microsynth AG, Balgach Switzerland). Libraries were constructed by ligating sequencing adapters and indices onto purified PCR products using the Nextera XT Sample Preparation Kit (Illumina) and equimolar amounts of each of the libraries were pooled and sequenced on an Illumina MiSeq Sequencing Platform. Sequence data were analyzed with the software package QIIME (Caporaso et al., 2010). Low quality sequences (q < 20) were filtered, chimeric sequences were excluded by using the USEARCH 6.1 database (Edgar, 2010) and sequences were clustered into operational taxonomic units (OTUs; 97% similarity) with the QIIME script “pick_open_reference_otus.py.” OTUs with less than 10 sequences were removed, resulting in 8285 OTUs, which were used for all downstream analysis. The representative sequences of the 50 most abundant OTUs over all sampling time points were classified against type strains using the Greengenes database (http://greengenes.lbl.gov) (DeSantis et al., 2006).
Microbial diversity analysis
Both alpha and beta diversity indices were used to estimate the microbiome diversity within—and between microbial communities. Calculations were done with the “summary.single” command in the software package mothur (http://www.mothur.org/; Kozich et al., 2013). Alpha diversity indices analysis included Chao1 index (richness estimate), abundance-based coverage estimator (ACE, richness estimate), Shannon's diversity, and Simpson's diversity index.
For the Bray-Curtis similarity, the dataset was rarefied to the minimum number of sequences per sample. Rarefaction curve was constructed based on the observed number of OTUs and nearly reached asymptotes for all samples (data not shown).
Principal component analysis was done with JMP® (Version 10.0.0, SAS Institute Inc., Cary, NC). Shared OTUs among gut sites at different age were plotted as Venn diagrams using the R environment (package “VennDiagram,” version 1.6.17.) (Chen, 2016). Heatmaps were created using JColorGrid (Joachimiak et al., 2006).
Statistical analysis
Statistically significant differences in relative abundance with regard to sampling sites and time were calculated using “metastats” in mothur, which is based on the homonymous bioinformatics program (White et al., 2009; Paulson et al., 2011). “Metastats” uses repeated t statistics and Fisher's tests on random permutations to handle sparsely-sampled features (White et al., 2009). Results were reported as a mean and standard deviation (SD). The significance level was set to P < 0.05. The P-values were adjusted with the Benjamini and Hochberg false discovery rate correction (FDR, q-value), and a q < 0.25 was considered significant (Lim et al., 2016). Furthermore, significant differences between the diversity estimators of the two groups were performed using the non-parametric Kruskal-Wallis-test followed by Mann-Whitney-test. PASW statistics 20, SPSS software (Chicago, Il., USA) was used for statistical analyses of diversity estimators.
Accession numbers
Sequencing data are available in the European Nucleotide Archive (ENA) database under the accession number PRJEB14860.
Results
Sequence analysis, phylum and OTU classification
Sequencing of 130 samples yielded 51,825,306 quality-controlled sequences, clustering into 8285 operational taxonomic units (OTUs; 0.03 distance level). Throughout all gut sites 24 phyla were identified with Firmicutes, Proteobacteria, and Tenericutes being the most abundant ones. In Figure S1A, Tables S1A–D, relative abundances of all phyla are delineated with respect to age and groups. The results showed that in the jejunum and cecum, Firmicutes and Proteobacteria were the dominating luminal and mucosal-associated phyla in all birds investigated (Tables S2, S3).
At the first day of life Proteobacteria were significantly higher in the jejunal (P = 0.0000, q = 0.0000) and cecal (P = 0.016; q = 0.059) mucosa of the birds and decreased thereafter, as no significant differences were found between samples from day 14 to day 28 of age (P = 0.140; q = 0.438 and P = 0.519; q = 0.955). On the contrary, Firmicutes were significantly lower at day 1 and increased thereafter (P = 0.001; q = 0.016 and P = 0.006; q = 0.055 in the jejunal and cecal mucosa, respectively).
For infected birds, relative abundances of bacterial phyla at the two sampling time points carried out post infection are represented in Figure S1B, Tables S4A–D. Figure 1 shows that the phylum Proteobacteria decreased while Firmicutes increased at either 21 (7 dpi) or 28 days of age (14 dpi). There was a significant decrease in Actinobacteria and Proteobacteria in the jejunal mucosa at 14 dpi (P = 0.006; q = 0.100 and P = 0.005; q = 0.100), while Firmicutes and Bacteroidetes were more abundant in the infected birds compared to the controls (P = 0.005; q = 0.100 and P = 0.023; q = 0.217, Table S4A). However, in the cecal content and cecal mucosa, Bacteroidetes (P = 0.001; q = 0.019) increased at 7 dpi, but decreased (P = 0.002; q = 0.026 and P = 0.005; q = 0.048) at 14 dpi in the infected birds compared with the controls, indicating that the Campylobacter infection modulates the jejunal and cecal phylum abundances in different ways.
Figure 1 Relative abundances (%) of the most abundant phyla in the infected birds compared with the controls at the two sampling points post infection of (A) jejunum and (B) cecum. Data are presented as the mean values and standard deviation (SD). JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i). In Table 1, the 50 most abundant OTUs from all birds are listed including the internal OTU number, relative abundance together with the reference strain and similarity (compared with strains of the Greengenes database). Relative OTUs abundances at different ages in all birds are shown in Tables S5A–D, S6A–D. The OTUs and species abundances sorted by age at the four gut sites of the birds are shown in the heatmaps of Figure S2. In total, the 50 most abundant OTUs accounted for 73.9% of all sequences and of those 42 OTUs differed significantly in their relative abundances over all gut sites independent of the age (Tables 2, 3). At the first day of age, a notable high relative abundance of OTU 1, 25, 27, and 35 (best type strain hits: Escherichia coli, Enterococcus faecalis, Clostridium paraputrificum, and Clostridium sartagoforme) were found in both jejunal and cecal mucosa (Tables S5A,C), whereas OTU 38 (best type strain hit: Acinetobacter johnsonii) was only abundant in the jejunal mucosa and OTU 42 (best type strain hit: C. paraputrificum) was only abundant in the cecal mucosa. All these abundant OTUs decreased by age. In the jejunal mucosa, OTU 1 was the most abundant (57.9%), followed by the other four OTUs which ranged between 2.6 and 7.9%. Similarly, in the mucosa of the cecum, OTU 1 was highly abundant (65.9%), followed by OTUs 27, 25, 35, and 42 which ranged between 7.8 and 3.3%.
Table 1 The 50 most abundant OTUs retrieved from different gut sites from all birds independent of the infection status.
OTUs No. of sequences Relative abundance (%) Best type strain hita Similarity (%)
OTU 1 642068 10.64 Escherichia coli (GU968184.1) 100
OTU 2 341923 5.66 Lactobacillus johnsonii (HM772969.1) 100
OTU 3 339288 5.62 Lactobacillus salivarius (NZ_AEBA01000145.1) 100
OTU 4 310060 5.14 Clostridium spp. (FJ808599.1) 87
OTU 5 273783 4.54 Enterococcus durans (FJ917726.1) 100
OTU 6 209121 3.46 Anaerotruncus colihominis (NR_027558.1) 100
OTU 7 208070 3.45 Eubacterium desmolans (L34618.1) 98
OTU 8 161864 2.68 Clostridium cellulolyticum (X71847.1) 87
OTU 9 157466 2.61 Spiroplasma lampyridicola (AY189134.1) 82
OTU 10 151864 2.52 Clostridium leptum (AJ305238.1) 97
OTU 11 130587 2.16 Eubacterium desmolans (L34618.1) 99
OTU 12 127446 2.11 Eubacterium desmolans (L34618.1) 98
OTU 13 120732 2.00 Clostridium papyrosolvens (NR_026102.1) 87
OTU 14 113436 1.88 Eubacterium coprostanoligenes (HM037995.1) 92
OTU 15 98491 1.63 Clostridium straminisolvens (NR_024829.1); Clostridium thermocellum (AB558166.1) 87
OTU 16 87863 1.46 Clostridium cellulolyticum (NC_011898.1) 87
OTU 17 70842 1.17 Bacillus subtilis (FJ608705.1) 94
OTU 18 67038 1.11 Lactobacillus reuteri (EU547311.1) 99
OTU 19 66212 1.10 Ruminococcus bromii (NR_025930.1) 94
OTU 20 65592 1.09 Eubacterium desmolans (L34618.1) 95
OTU 21 53133 0.88 Clostridium cellulolyticum (NC_011898.1); Clostridium papyrosolvens (NR_026102.1) 87
OTU 22 49736 0.82 Clostridium thermocellum (AB558166.1) 85
OTU 23 47570 0.79 Clostridium thermosuccinogenes (Y18180.1); Clostridium thermocellum (AB558166.1) 86
OTU 24 40373 0.67 Clostridium leptum (AJ305238.1) 95
OTU 25 36925 0.61 Enterococcus faecalis (FJ607291.1) 100
OTU 26 35311 0.58 Proteus mirabilis (GU477712.1) 100
OTU 27 31154 0.52 Clostridium paraputrificum (AY442815.1) 100
OTU 28 29186 0.48 Variovorax paradoxus (HQ005421.1) 100
OTU 29 28876 0.48 Campylobacter subsp. jejuni (NC_008787.1) 100
OTU 30 27988 0.46 Clostridium leptum (AJ305238.1) 93
OTU 31 23587 0.39 Anaerotruncus colihominis (NR_027558.1) 93
OTU 32 23559 0.39 Lactobacillus crispatus (FN692037.1) 100
OTU 33 22863 0.38 Phyllobacterium myrsinacearum (AY785330.1) 100
OTU 34 21547 0.36 Catabacter hongkongensis (AY574991.1); Clostridium thermosuccinogenes (Y18180.1) 86
OTU 35 20378 0.34 Clostridium sartagoforme (FJ384380.1) 100
OTU 36 18849 0.31 Acetivibrio cellulolyticus (L35515.1) 95
OTU 37 18055 0.30 Clostridium papyrosolvens (NR_026102.1) 86
OTU 38 17890 0.30 Acinetobacter johnsonii (EU977694.1) 100
OTU 39 15658 0.26 Clostridium papyrosolvens (NR_026102.1) 87
OTU 40 15361 0.25 Lactobacillus johnsonii (EU381128.1) 96
OTU 41 15143 0.25 Clostridium thermosuccinogenes (Y18180.1) 87
OTU 42 14985 0.25 Clostridium paraputrificum (AY442815.1) 100
OTU 43 14682 0.24 Marinobacter sp. (FJ889664.1) 99
OTU 44 14652 0.24 Clostridium papyrosolvens (NR_026102.1) 87
OTU 45 14304 0.24 Shigella flexneri (CP000266.1) 99
OTU 46 13619 0.23 Clostridium cellulolyticum (NC_011898.1) 86
OTU 47 13307 0.22 Clostridium papyrosolvens (NR_026102.1) 86
OTU 48 13152 0.22 Clostridium papyrosolvens (NR_026102.1) 87
OTU 49 12978 0.21 Clostridium papyrosolvens (NR_026102.1) 87
OTU 50 12418 0.21 Lactobacillus salivarius (NZ_AEBA01000145.1) 98
a Greengenes best type strain hit accession numbers are listed in parenthesis.
Table 2 Relative abundances (%) of the most abundant OTUs in different gut sites of control birds (day 1–28).
OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC
Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa
OTU 49 0 0.02 0.05 0.11 0.01 0.02 0.01 0.02 0.056 0.164 0.655 0.858 0.366 0.623 0.133 0.326
OTU 25 1.89 4.01 0.06 0.07 1.05 2.95 0.01 0.02 0.001 0.011 0.015 0.067 0.365 0.623 0.001 0.011
OTU 5 12.41 25.84 13.09 21.85 0.28 0.56 0.07 0.09 0.920 0.990 0.039 0.134 0.002 0.017 0.001 0.011
OTU 30 0.45 1.45 0.40 0.72 0.74 1.11 1.25 2.09 0.913 0.990 0.385 0.643 0.808 0.946 0.059 0.170
OTU 9 0.90 2.72 1.03 3.05 3.56 9.78 5.82 15.04 0.938 0.990 0.514 0.765 0.196 0.401 0.091 0.244
OTU 13 1.34 5.22 0.75 1.84 1.36 4.51 1.41 4.43 0.714 0.890 0.831 0.946 0.940 0.990 0.549 0.770
OTU 15 0.07 0.20 0.13 0.32 1.17 1.98 4.21 9.38 0.792 0.942 0.095 0.250 0.005 0.030 0.001 0.011
OTU 18 2.36 8.46 2.34 6.03 0.08 0.23 0.03 0.09 0.961 0.994 0.409 0.665 0.081 0.220 0.013 0.059
OTU 21 0.65 2.01 0.32 0.87 0.53 1.11 1.08 3.21 0.588 0.787 0.599 0.796 0.812 0.946 0.294 0.526
OTU 33 0.96 1.38 2.57 5.92 0 0 0 0 0.341 0.603 0.001 0.011
OTU 12 0.95 2.20 1.25 4.71 2.42 5.21 5.41 11.82 0.776 0.929 0.285 0.519 0.491 0.739 0.131 0.326
OTU 28 3.21 7.19 2.99 7.77 0 0 0 0 0.941 0.990 0.006 0.034 0.001 0.011 0.001 0.011
OTU 37 0.12 0.56 0 0.01 0.39 1.93 0.07 0.28 0.140 0.326 0.939 0.990 0.947 0.991 0.177 0.379
OTU 40 0.05 0.11 1.08 1.53 0 0 0.10 0.44 0.001 0.011 0.464 0.722 0.001 0.011 0.008 0.043
OTU 3 10.36 20.66 18.43 23.28 0.39 0.63 1.52 5.30 0.252 0.475 0.517 0.765 0.001 0.011 0.002 0.017
OTU 26 0.03 0.07 0.03 0.06 1.34 2.35 1.75 3.25 0.483 0.737 0.691 0.875 0.001 0.011 0.003 0.020
OTU 19 0.80 1.99 0.22 0.57 1.09 2.22 1.01 2.17 0.189 0.395 0.979 0.997 0.961 0.994 0.134 0.326
OTU 44 0.04 0.15 0.02 0.04 0.06 0.12 0.07 0.14 0.748 0.908 0.660 0.858 0.452 0.715 0.052 0.155
OTU 39 0.02 0.07 0.01 0.02 0.07 0.20 0.08 0.19 0.769 0.927 0.726 0.893 0.253 0.475 0.046 0.147
OTU 29 0 0 0 0 0 0 0 0 0.002 0.017
OTU 2 10.86 14.76 24.38 24.19 0.13 0.26 0.31 1.13 0.046 0.147 0.817 0.946 0.001 0.011 0.001 0.011
OTU 38 1.51 5.31 0.17 0.67 0 0 0 0 0.145 0.326 0.002 0.017
OTU 42 0.51 1.20 0.01 0.03 0.67 1.71 0.01 0.03 0.012 0.057 0.041 0.136 0.717 0.890 0.669 0.864
OTU 17 0.46 1.30 0.02 0.05 2.79 7.57 0.05 0.15 0.041 0.136 0.063 0.176 0.243 0.466 0.571 0.770
OTU 1 14.87 24.08 5.33 7.93 22.17 26.59 13.03 17.69 0.069 0.190 0.231 0.452 0.295 0.526 0.062 0.176
OTU 11 0.69 1.32 0.51 0.97 2.63 7.62 3.10 5.11 0.362 0.623 0.692 0.875 0.458 0.719 0.003 0.020
OTU 4 0.51 2.00 0.17 0.56 1.34 4.60 2.14 7.58 0.571 0.770 0.611 0.806 0.525 0.770 0.147 0.326
OTU 48 0 0 0 0 0 0 0 0 0.036 0.131
OTU 14 0.24 0.69 0.22 0.43 3.77 8.30 4.66 10.97 0.542 0.770 0.747 0.908 0.023 0.091 0.004 0.025
OTU 46 0 0.02 0.01 0.02 0.26 0.65 0.25 0.50 0.348 0.609 0.991 1.000 0.028 0.106 0.039 0.134
OTU 31 0.23 0.55 0.05 0.12 0.87 1.67 0.33 0.51 0.137 0.326 0.170 0.368 0.166 0.364 0.016 0.068
OTU 45 0.05 0.09 0.01 0.01 0.35 0.56 1.02 1.62 0.023 0.091 0.096 0.250 0.016 0.068 0.004 0.025
OTU 10 0.37 1.03 0.20 0.46 4.39 11.22 4.97 10.40 0.477 0.736 0.824 0.946 0.013 0.059 0.003 0.020
OTU 32 0.12 0.43 0.23 0.79 0 0 0 0 0.540 0.770 0.868 0.975 0.012 0.057 0.006 0.034
OTU 8 0.28 1.29 0.03 0.10 1.43 5.01 2.34 7.10 0.537 0.770 0.551 0.770 0.370 0.624 0.138 0.326
OTU 6 1.17 3.54 0.13 0.28 9.20 15.81 1.39 1.56 0.238 0.461 0.007 0.039 0.021 0.087 0.001 0.011
OTU 36 0.03 0.11 0.11 0.22 0.68 1.66 0.25 0.49 0.144 0.326 0.263 0.488 0.003 0.020 0.220 0.445
OTU 35 0.57 1.28 0.02 0.04 0.90 2.13 0.02 0.08 0.012 0.057 0.034 0.126 0.542 0.770 0.867 0.975
OTU 7 1.07 2.73 1.41 2.66 3.52 7.28 6.47 12.19 0.832 0.946 0.282 0.518 0.125 0.320 0.037 0.132
OTU 16 0.73 3.50 0.27 1.01 1.41 3.77 1.96 4.92 0.905 0.990 0.562 0.770 0.400 0.656 0.146 0.326
OTU 27 0.98 2.31 0.02 0.07 1.56 4.02 0.01 0.05 0.012 0.057 0.048 0.151 0.563 0.770 0.719 0.890
OTU 20 1.68 4.52 0.05 0.18 0.86 4.28 0.91 4.07 0.049 0.151 0.981 0.997 0.448 0.715 0.997 1.000
OTU 50 0.09 0.15 0.84 0.95 0 0.01 0.06 0.23 0.001 0.011 0.486 0.737 0.001 0.011 0.002 0.017
OTU 22 0 0 0 0.02 0 0 0 0.01 0.231 0.452 0.882 0.985
OTU 47 0.12 0.53 0 0.02 0.32 1.55 0.06 0.22 0.191 0.395 0.917 0.990 0.933 0.990 0.180 0.381
OTU 41 0 0.01 0 0 0 0 0 0 0.228 0.452 1.000 1.000
OTU 23 0.12 0.50 0.01 0.02 0.07 0.20 0.09 0.23 0.136 0.326 0.682 0.874 0.819 0.946 0.024 0.093
OTU 43 0.01 0.03 0 0 0 0 0 0
OTU 34 0.03 0.14 0 0 0.06 0.16 0.14 0.38 0.903 0.990 0.417 0.672 0.390 0.645 0.051 0.155
OTU 24 0.11 0.52 0.18 0.39 1.18 1.89 1.10 1.90 0.567 0.770 0.973 0.997 0.001 0.011 0.003 0.020
a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold.
Table 3 Relative abundances (%) of the most abundant OTUs in different gut sites of infected birds (days 21 and 28).
OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC
Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa
OTU 49 0.18 0.28 0.43 0.98 0.61 1.44 0.52 0.91 0.689 0.880 0.936 0.989 0.550 0.791 0.516 0.776
OTU 25 0.02 0.04 0.08 0.09 0.00 0.00 0 0 0.077 0.178 0.063 0.168
OTU 5 1.65 2.21 8.89 6.18 0.01 0.01 0 0 0.009 0.043 0.761 0.927 0.001 0.007 0.001 0.007
OTU 30 0.31 0.94 0.06 0.08 0.30 0.38 0.16 0.12 0.957 0.989 0.355 0.596 1.000 1.000 0.013 0.056
OTU 9 0.17 0.39 0.14 0.14 1.47 4.29 2.06 5.88 0.903 0.987 0.575 0.791 0.530 0.785 0.217 0.408
OTU 13 0.64 1.06 0.72 1.35 2.87 3.77 2.65 2.58 0.955 0.989 0.950 0.989 0.056 0.159 0.020 0.071
OTU 15 0.08 0.13 0.01 0.02 1.24 0.89 2.13 1.23 0.049 0.146 0.040 0.126 0.001 0.007 0.001 0.007
OTU 18 4.67 9.39 6.34 11.77 0.19 0.44 0.14 0.36 0.572 0.791 0.857 0.986 0.102 0.218 0.011 0.051
OTU 21 0.28 0.58 0.16 0.19 1.63 2.60 1.93 2.41 0.565 0.791 0.611 0.611 0.085 0.191 0.009 0.043
OTU 33 1.11 1.14 0.13 0.13 0.00 0.00 0.00 0.00 0.008 0.041 1.000 1.000 0.001 0.007 0.001 0.007
OTU 12 0.51 0.74 0.06 0.08 0.06 0.09 0.05 0.05 0.056 0.159 0.929 0.989 0.062 0.168 0.796 0.949
OTU 28 1.19 1.20 0.20 0.21 0.00 0.00 0.00 0.00 0.015 0.060 0.016 0.060 0.001 0.007 0.001 0.007
OTU 37 0.14 0.27 0.01 0.02 0.35 0.18 0.51 0.27 0.074 0.178 0.077 0.178 0.207 0.394 0.001 0.007
OTU 40 0.07 0.08 1.35 0.83 0.01 0.01 0.00 0.01 0.001 0.007 0.881 0.987 0.008 0.041 0.001 0.007
OTU 3 11.02 13.33 29.61 19.69 0.52 0.56 0.41 0.45 0.067 0.173 0.865 0.986 0.004 0.023 0.001 0.007
OTU 26 0 0 0.01 0.05 0.01 0.01 0.01 0.01 0.542 0.791 0.801 0.949 0.070 0.176 0.990 1.000
OTU 19 0.14 0.29 0.31 0.24 3.24 7.48 2.09 5.77 0.372 0.613 0.614 0.823 0.107 0.223 0.441 0.700
OTU 44 0.43 1.20 0.07 0.12 0.49 0.94 1.06 2.17 0.594 0.809 0.574 0.791 0.552 0.791 0.014 0.059
OTU 39 0.02 0.05 0.13 0.20 0.59 0.79 1.02 1.34 0.072 0.178 0.318 0.539 0.001 0.007 0.016 0.060
OTU 29 0.30 0.66 0.01 0.03 3.92 6.25 0.38 0.51 0.052 0.152 0.049 0.146 0.036 0.115 0.005 0.028
OTU 2 19.98 22.32 23.46 10.10 0.85 1.46 0.19 0.30 0.834 0.975 0.285 0.493 0.002 0.012 0.001 0.007
OTU 38 0 0.01 0 0 0 0 0 0 0.690 0.012
OTU 42 0 0 0 0 0 0 0 0
OTU 17 0.62 1.33 0.25 0.31 4.45 6.58 0.12 0.18 0.451 0.703 0.002 0.012 0.091 0.201 0.531 0.785
OTU 1 0.11 0.18 0.81 1.36 0.28 0.40 0.19 0.36 0.145 0.292 0.760 0.927 0.280 0.491 0.255 0.455
OTU 11 1.09 1.39 0.10 0.10 2.01 2.44 2.31 3.56 0.026 0.086 0.761 0.927 0.907 0.987 0.007 0.038
OTU 4 3.43 6.60 0.13 0.11 12.51 8.03 16.82 10.92 0.154 0.303 0.162 0.315 0.016 0.060 0.001 0.007
OTU 48 0.41 1.14 0.01 0.02 2.29 7.23 0.38 1.17 0.225 0.414 0.747 0.927 0.817 0.962 0.222 0.413
OTU 14 0.24 0.65 0.07 0.07 0.45 0.84 1.41 2.08 0.364 0.606 0.122 0.251 0.619 0.824 0.076 0.178
OTU 46 0.21 0.60 0.01 0.02 0.49 0.81 0.52 0.87 0.306 0.524 0.757 0.927 0.396 0.646 0.016 0.060
OTU 31 0.03 0.06 0.03 0.04 0.37 0.52 0.08 0.07 0.955 0.989 0.057 0.159 0.012 0.055 0.019 0.068
OTU 45 0 0 0 0 0 0 0 0 1.000 1.000 0.281 0.491
OTU 10 0.26 0.82 0.09 0.12 0.29 0.57 0.22 0.30 0.960 0.989 0.896 0.987 0.891 0.987 0.175 0.336
OTU 32 2.90 3.72 3.80 3.98 0.18 0.46 0.05 0.11 0.872 0.986 0.567 0.791 0.004 0.023 0.001 0.007
OTU 8 1.21 2.88 0.05 0.09 7.75 7.99 6.25 8.70 0.036 0.115 0.917 0.989 0.021 0.073 0.001 0.007
OTU 6 0.82 1.99 0.10 0.13 4.11 2.46 1.24 1.97 0.455 0.703 0.026 0.086 0.019 0.068 0.001 0.007
OTU 36 0.21 0.40 0.23 0.21 0.34 0.37 0.19 0.22 0.893 0.987 0.441 0.700 0.473 0.724 0.871 0.986
OTU 35 0 0 0 0 0 0 0 0
OTU 7 0.24 0.40 0.08 0.17 4.65 13.62 6.23 18.65 0.095 0.205 0.692 0.880 0.501 0.760 0.062 0.168
OTU 16 0.19 0.27 0.29 0.47 1.37 1.80 1.55 1.94 0.776 0.932 0.653 0.862 0.074 0.178 0.048 0.146
OTU 27 0 0 0 0 0 0 0 0
OTU 20 0.22 0.67 0.03 0.05 4.32 13.62 0.62 1.88 0.849 0.986 0.770 0.932 0.576 0.791 0.424 0.686
OTU 50 0.10 0.17 1.20 0.73 0.01 0.01 0.01 0.01 0.001 0.007 0.979 1.000 0.013 0.056 0.001 0.007
OTU 22 0.14 0.42 0 0 2.08 5.32 3.60 9.82 0.107 0.223 0.671 0.877 0.236 0.430 0.001 0.007
OTU 47 0.03 0.06 0.01 0.01 0.20 0.10 0.31 0.23 0.244 0.440 0.092 0.201 0.001 0.007 0.001 0.007
OTU 41 0.99 2.99 0 0 0.50 0.87 1.28 3.32 0.723 0.913 0.923 0.989
OTU 23 0.63 1.18 0.02 0.02 2.39 2.31 2.88 2.65 0.124 0.252 0.448 0.703 0.064 0.168 0.001 0.007
OTU 43 8.90 28.14 0 0 0 0 0 0
OTU 34 0.02 0.05 0 0 0.85 0.79 1.54 1.09 0.148 0.294 0.068 0.173 0.001 0.007 0.001 0.007
OTU 24 0 0 0.05 0.07 0.15 0.13 0.12 0.11 0.674 0.877 0.082 0.187
a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. The OTUs and species abundances sorted by gut sites of the infected birds compared with the control birds are shown in the heatmaps (Figure 2). Interestingly, in the infected birds, the abundance of E. coli and Eubacterium desmolans (best type strain hits) were lower at different gut sites (Figure 3A). On the contrary, Clostridium spp. abundance was higher in the infected birds compared with the negative controls (Figure 3B).
Figure 2 Heatmap showing the relative abundances (%) of the 50 most-abundant OTUs sorted by gut sites of the infected birds compared with the controls at the two sampling points post infection. The heat map integrates relative abundance of a given phylotype. Colour scaling is ranged from 0 to ≥ 25%. n.d, not detected.
Figure 3 Relative abundances (%) of the most relevant OTUs in the infected birds compared with the controls at the two sampling points post infection (A) OTUs 1 and 12, (B) OTUs 4 and 29. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content.
Assessment of the microbial community diversity
Diversity indices estimating species richness and evenness for birds are shown in Figure 4. Diversity indices indicated that microbial richness and diversity increased with age. Interestingly, diversity indices were not different comparing samples from days 1 and 7. However, older chickens (14–28 days of age) had a significantly more diverse microbial community structure as indicated by the number of OTUs observed (Sobs), Chao1, ACE, Shannon's index, and Simpson index (P < 0.01). In addition, the microbial diversity in older chickens is more consistent, as there was no difference in diversity indices comparing samples from days 14 to 28. The results also revealed significant differences in the microbial diversity among jejunum and cecum as the chicken aged, supported by Sobs (P < 0.001), Chao1 (P < 0.001), ACE (P < 0.001), Shannon's index (P < 0.001), and Simpson index (P = 0.060) with a more complex diversity in the cecum compared with the jejunum. Furthermore, a difference in species richness among the luminal and mucosa-associated gut microbiota, independent of the age, was detected in all birds as supported by Sobs (P = 0.017), Chao1 (P = 0.015), ACE (P = 0.022), respectively.
Figure 4 Species richness and diversity measures of the microbial community at all gut sites in the control (A), infected birds (B), and (C) species richness and diversity estimates for bacteria from cecum content of the infected birds compared with the controls. Left Y-axis for number of observed OTUs (Sobs), Chao 1 and ACE, and Right Y-axis for Shannon and Simpson. Significant differences were calculated with Kruskal-Wallis-tests and Mann-Whitney-tests, and significance was declared at P < 0.05. Data are presented as the mean values and SD. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. In the infected birds, significant differences in the microbial diversity among jejunum and cecum supported by Sobs (P < 0.001), Chao1 (P < 0.001), ACE (P < 0.001), Shannon's index (P < 0.001), and Simpson index (P = 0.011) were found. Additionally, an increase in the species richness among luminal and mucosa-associated gut microbiota of the infected birds at 14 dpi compared with those from 7 dpi was obtained. Diversity indices were not significantly different among the gut sites of infected and control birds. Exceptional to this, a higher species richness was noticed in the cecum content of infected birds at 14 dpi, supported by Sobs, Chao1, and ACE (P = 0.047, Figure 4C), indicating that the Campylobacter infection increased the microbiota complexity.
Similarity and stability of the gut microbiota composition over time
The microbial community similarity among all samples over time was assessed by calculating a Bray-Curtis similarity matrix. Community similarity analysis based on the Bray-Curtis index showed clear differences between gut sites and age, indicating strong shifts in microbial community structures (Figure 5). In addition, the Bray-Curtis index suggested that the birds at the first day of age displayed a high degree of dissimilarity compared with the other ages. It was also apparent that microbiota compositions of older birds were more similar compared with young birds.
Figure 5 Microbial community similarity between all samples calculated with Bray-Curtis similarities, which displays the similarity results between the control and infected groups according to age and gut sites. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. The Bray-Curtis index revealed clear differences between jejunum and cecum from infected birds at the two sampling time points post infection. Furthermore, the comparison of the microbiota between control and infected birds showed that community structures were more dissimilar at the OTUs level, demonstrating that the gut microbial communities changed as a result of infection.
To measure the similarity between microbial communities in all birds at different ages, principal component analysis (PCA) was performed (Figure 6). PCA analysis showed that there was a clear clustering of the birds at days 1 and 7 of age in the jejunum and cecum compared with the other days. In addition, the microbial community of the older chickens clustered with less variation compared to young birds. PCA plots also demonstrate that, the microbial community was more separated in the ceca than in the jejunum.
Figure 6 Principal component analysis (PCA) was analyzed for the control (A) and infected birds (B). Orange (day 1), Red (day 7), Green (day 14), Blue (day 21), and Black (day 28). Each symbol indicates an individual bird. All PCA plots include the data of all samples; symbols not belonging to the sample group indicated in the header are displayed faded. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. To delineate the shared species among the groups, a Venn diagram displaying the overlaps between gut sites at different ages and groups was performed (Figure S3). The proportions of shared OTUs appear to be low at each gut site from day 1 to day 28 of age. These shared species, however, varied from one site to another.
Furthermore, the analysis showed that only 399 OTUs (n = 1847 OTUs) were shared among the jejunal mucosa in the control and infected birds, while 745 OTUs (n = 2401 OTUs) were shared between the jejunal content in the control and infected birds at the two time points post infection (Figure 7A). In the cecal mucosa and the cecal content, the comparison revealed that only 2218 OTUs (n = 6736 OTUs) and 2617 OTUs (n = 6860 OTUs) were shared, among control and infected birds combining the two time points post infection (Figure 7B). These data demonstrated that 25–36% of the observed OTUs in the jejunum and cecum were shared between the control and infected birds, respectively.
Figure 7 Venn diagrams showing the shared OTUs between the control and infected birds at different gut sites at the two sampling points post infection (A) jejunum; (B) cecum. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i); d, day.
Discussion
The intestinal microbiota acts as a physical barrier for incoming pathogens and plays an important role in the host resistance against infections by both direct interactions with pathogenic bacteria via competitive exclusion, such as occupation of attachment sites or consumption of nutrient sources, and indirectly by influencing the immune system via production of antimicrobial substances (Sekirov et al., 2010). Development of the gut microbiota in chickens occurs immediately after hatching and by getting older, this microbiome becomes very diverse until it reaches a relatively stable dynamic state (Pan and Yu, 2014).
Interactions of the intestinal microbiome with the host and certain microorganisms have profound effects on bird health, and are therefore of great importance for poultry production. Consequently, in the present study, the composition of the gut microbiota of chickens in a longitudinal study from day 1 to day 28 of age was analyzed and the differences between content and mucosa-associated gut microbiota were investigated. In order to extend the range of analyses comparisons were performed between control chickens and chickens infected at 14 days of age with C. jejuni.
In this study, a high diversity of phyla (15 in the jejunal and 4 in the cecal mucosal samples) was found at day 1 of life, indicating a rapid intake of environmental organisms after birth. In addition, the composition of the gut microbiota differed substantially between young and older birds, with Proteobacteria being significantly more present at the first day of life and decreasing thereafter, whereas the Firmicutes were the predominant phylum in older birds. This is in agreement with Lu et al. (2003) who found that the gut is firstly colonized by the phylum Proteobacteria, particularly by the family Enterobacteriaceae. In older birds, the phylum Firmicutes mainly represented by Lachnospiraceae, Ruminococcaceae, Clostridiaceae, and Lactobacillaceae dominated. As a consequence, the chicken gut is firstly colonized by facultative aerobes which are substituted later on by anaerobes. Obviously, oxygen consumption by the aerobic bacteria alters the gut ecosystem toward more reducing conditions, which facilitates subsequent growth and colonization of the obligate anaerobes (Wise and Siragusa, 2007).
Besides Proteobacteria and Firmicutes, also lower abundant phyla (e.g., Actinobacteria and Tenericutes) changed significantly with time, indicating high dynamics in the re-organization of the whole microbiome through time. Taken together, the present study revealed that the chicken gut is largely dominated by the phyla Proteobacteria and Firmicutes, with lower proportions of Actinobacteria, Bacteroidetes, and Tenericutes. Similarly, previous studies have also shown that Firmicutes, Bacterioidetes, and Proteobacteria are the most common phyla in the chicken ceca (Wei et al., 2013; Oakley et al., 2014; Sergeant et al., 2014).
Interestingly, jejunal, and cecal microbiota were found to be distinct and certain acid-tolerant bacteria, mostly Acidobacteria, were present in the jejunum only. Altogether, the results demonstrated that the abundance of bacteria varied between the jejunum and the cecum, with some species more present in the jejunum (e.g., Acinetobacter and Acidobacteria) and others (e.g., Bacteroides and Clostridium) being predominant in the cecum of chickens. This and other variations can be explained by the fact that feed passes quickly through the foregut and is retained for hours in the hindgut. In addition, the small intestine is mainly responsible for food digestion and absorption, while the large intestine, especially the cecum, is responsible for microbial fermentation, further nutrient absorption and detoxification of substances that are harmful to the host (Gong et al., 2002).
Chickens investigated in the current study had a high abundance of E. coli and E. faecalis (best type strain hits) in the first week of life which might potentially increase their resistance to other bacterial infections. E. coli, a facultative anaerobe bacterium, was the dominant species in the early life of chickens. Thus, a depletion of E. coli during the second week of life could potentially affect the host susceptibility to enteric pathogen infections, representing a key role for these gut microbiota in host resistance. This decrease in E. coli abundance has been attributed with a beginning dominance of anaerobes (Zhu and Joerger, 2003). It may be possible that such disturbances in the community structure allow a pathogen to colonize and proliferate. Anyhow, it remains hypothetical whether these diversity changes influence the susceptibility to pathogens and the outcome of infection.
The current results revealed that E. coli, E. faecalis, C. paraputrificum, and C. sartagoforme (best type strain hits) were more predominant in the mucosa than in the lumen, suggesting significant implications for birds' health, considering that the mucosa-associated bacteria are of great importance in the host mucosal responses with consequences for the mucosal barrier (Ott et al., 2004).
Despite the high prevalence of Campylobacter in chickens the mechanism of colonization in the gut is still poorly understood. The high bacterial load in the gut and the establishment of a latent infection characterized by continuous shedding indicates that Campylobacter in chickens can modify the microbiota composition. In the current study it could be shown that Campylobacter colonization shifted the two major phyla towards an enrichment of Firmicutes with concomitant reduction of Proteobacteria. Interestingly, a reverse correlation between Firmicutes and Proteobacteria was observed, suggesting a possible antagonistic interaction between these two phyla. According to Pan and Yu (2014) alterations in one phyla or species may not only affect the host directly, but can also disrupt the entire microbial community. Notably, bacterial taxa belonging to the phyla Firmicutes are known to be involved in the degradation of complex carbohydrates (not absorbed by the host) and in the production of SCFAs (Thibodeau et al., 2015). Thus, the SCFAs production by Firmicutes might, at least partially, explain their dominance in the infected birds, which have a high SCFAs requirement as a source of energy for C. jejuni to colonize the chicken gut. Furthermore, Brown et al. (2012) reported that members of the phylum Firmicutes can inhibit the growth of opportunistic pathogens, such as E. coli, which has also been shown in the present study.
Besides these major shifts, also low abundant phyla (e.g., Actinobacteria and Tenericutes) were affected by the Campylobacter infection, which could also disequilibrate the microbiome composition. Similarly, Johansen et al. (2006) found in a denaturing gradient gel electrophoresis (DGGE) based experiment that C. jejuni colonization affected the development and complexity of the microbial communities of the ceca over 17 days of age. Furthermore, Qu et al. (2008) noted that the community structure of the cecal microbiome from the C. jejuni challenged chicken has greater diversity and evenness with a higher abundance of Firmicutes at the expense of the Bacteroidetes and other taxa. Sofka et al. (2015) also reported that Campylobacter carriage, assessed in samples from slaughter houses, was associated with moderate modulations of the cecal microbiome as revealed by an increase in Streptococcus and Blautia relative abundance in birds of 56 days of age, originating from different farms and production types. Recently, Thibodeau et al. (2015) found also that C. jejuni colonization induced a moderate alteration of the chicken cecal microbiome beta-diversity at 35 days of age.
This study's results strongly suggest that the Campylobacter associated alterations of the gut microbiota were a direct effect due to the interaction of C. jejuni with the microbiota or a consequence of the host responses or even a combination of both (Barman et al., 2008; Mon et al., 2015). The obtained results indicate that the influence of a Campylobacter infection on microbial communities was more pronounced at 14 dpi than at 7 dpi. This could be explained by an increased load of Camplyobacter at the later time point as demonstrated in recent studies using the same C. jejuni strain (Awad et al., 2014, 2015a,b, 2016).
We also found significant differences in the abundance of certain bacterial species in the infected birds compared with the controls. C. jejuni caused a significant decrease in E. coli (best type strain hit) in the microbiota of infected birds in both jejunum and cecum. This is in agreement with our previous study which showed that Campylobacter colonization decreased E. coli loads in the jejunum and cecum at 7 dpi and at 14 dpi, but increased E. coli translocation to the liver and spleen of the infected birds as determined by conventional bacteriology (Awad et al., 2016). Thus, the current results pointed out that the relative abundance of E. coli could be an important determinant of susceptibility for a Campylobacter infection in particular and Gram-negative pathogens in general.
In contrast to the Campylobacter -E. coli interaction, it was found that the relative abundance of Clostridium spp. was higher in the infected birds compared with the negative controls, indicating a link between C. jejuni and Clostridium. This confirms data from an earlier study in which a positive correlation between high levels of Clostridium perfringens (>6 log) and the colonization of C. jejuni were found by real-time quantitative PCR (Skånseng et al., 2006; Thibodeau et al., 2015). This might be due to the fact that C. jejuni acts as a hydrogen sink leading to improved growth conditions for some Clostridia through increased fermentation (Kaakoush et al., 2014). This link can also be explained by the fact that the Clostridium organic acid production could be used by C. jejuni as an energy source. Furthermore, it was found that a Campylobacter infection induces excess mucous production in the intestine (Molnár et al., 2015) which consequently may enhance Clostridium proliferation due to the fact that an increase in mucin secretion in the gut provides an opportunity for Clostridium spp. to proliferate (M'Sadeq et al., 2015). Overall, the higher abundance of Campylobacter and Clostridium spp. might result in a higher endotoxin production with subsequent increase in intestinal permeability that facilitates the colonization and enhances bacterial translocation from the intestine to the internal organs, which is well in agreement with our pervious results (Awad et al., 2015a, 2016).
Finally, the strong shifts in the bacterial microbiome in the current study might help to explain why a Campylobacter infection is age dependent and chickens in the field become mainly colonized at an age of two to 4 weeks (Newell and Fearnley, 2003; Conlan et al., 2007). In agreement with this, Bereswill et al. (2011) demonstrated that a shift of intestinal microbiota in humans was linked with an increased susceptibility for C. jejuni. Finally, Haag et al. (2012) demonstrated that C. jejuni colonization in mice depends on the microbiota of the host and vice versa and Campylobacter colonization induces a shift of the intestinal microbiota. This was also observed in the present study as community structures were more dissimilar at the OTUs level in the infected birds compared with the controls. Moreover, in the infected birds, the population of beneficial microbes, such as E. coli and E. desmolans were comparatively lower than the potentially pathogenic bacteria, such as Clostridium spp., rendering the need for modulation of the gut microbiota to improve the gut health of the infected birds.
Conclusion
In the current study a substantial change in the composition of luminal and mucosa-associated gut microbiota in broiler chickens from day 1–28 was noticed. It could also be demonstrated that a C. jejuni infection in chickens was associated with significant changes in the composition of the intestinal ecosystem. Furthermore, these changes of the gut microbiota could lead to intestinal dysfunction, which has been evidenced in our previous studies. In this context, the results provide new insights into the microecological divergence of the intestinal microbiota with and without a Campylobacter infection and illustrate the C. jejuni–host crosstalk within the gut of broiler chickens. Understanding the relationship between disruption of the normal gut microbiota and Campylobacter infection may lead to improve in control strategies in order to minimize the consequences for the chicken host and the risk of bacterial spread to humans.
Author contributions
All authors listed, have made substantial, direct and intellectual contribution to the work, and approved it for publication.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Part of this work was performed within the CEPO (Centre of Excellence for Poultry) project, which was funded by the European Regional Development Fund, Cross-border Cooperation Programme Austria–Hungary 2007–2013. Grant No: L00112. Our special acknowledgement to Dr. Alexander Tichy (Bioinformatics and Biostatistics Platform, Department of Biomedical Sciences, University of Veterinary Medicine Vienna) for his assistance with the statistical analyses. Furthermore, we would like to thank all staff who assisted with the animal infection experiments at the Clinic for Poultry and Fish Medicine, University of Veterinary Medicine Vienna.
Supplementary material
The Supplementary Material for this article can be found online at: http://journal.frontiersin.org/article/10.3389/fcimb.2016.00154/full#supplementary-material
Figure S1 Relative abundances (%) of the most abundant bacterial phyla of (A) control and (B) infected birds. Data are presented as the mean values and SD. Left Y-axis for Firmicutes, Proteobacteria and others (unclassified); Right Y-axis for Tenericutes, Acidobacteria, Actinobacteria, Bacteroides, and Cyanobacteria. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content.
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Figure S2 Heatmap showing the relative abundances of the 50 most-abundant OTUs sorted by gut sites and age in the control birds. The heat map shows relative abundance of a given phylotype. Colour scaling is ranged from 0 to higher than 25%. n.d, not detected; n.a, not analyzed.
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Figure S3 Venn diagrams are showing the shared OTUs for the control at different gut sites from day 1–28 (A) jejunum; (B) cecum. jm, jejunal mucosa; jc, jejunal content; cm, cecum mucosa; cc, cecum content; (c), control; (i), infected; d, day.
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Table S1 Relative abundances (%) of bacterial phyla in the control birds from day 1–28 (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content.
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Table S2 Relative abundances (%) of bacterial phyla in different gut sites of control birds (day 1–28).
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Table S3 Relative abundances (%) of bacterial phyla in different gut sites of infected birds (days 21 and 28).
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Table S4 Relative abundances (%) of bacterial phyla in the infected birds at the two sampling points post infection (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content.
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Table S5 The 50 most abundant OTUs in the control birds from day 1–28 (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content.
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Table S6 The 50 most abundant OTUs in the infected birds at the two sampling points post infection (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, and (D) cecal content.
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article-title | Age-Related Differences in the Luminal and Mucosa-Associated Gut Microbiome of Broiler Chickens and Shifts Associated with Campylobacter jejuni Infection |
abstract | Despite the importance of gut microbiota for broiler performance and health little is known about the composition of this ecosystem, its development and response towards bacterial infections. Therefore, the current study was conducted to address the composition and structure of the microbial community in broiler chickens in a longitudinal study from day 1 to day 28 of age in the gut content and on the mucosa. Additionally, the consequences of a Campylobacter (C.) jejuni infection on the microbial community were assessed. The composition of the gut microbiota was analyzed with 16S rRNA gene targeted Illumina MiSeq sequencing. Sequencing of 130 samples yielded 51,825,306 quality-controlled sequences, which clustered into 8285 operational taxonomic units (OTUs; 0.03 distance level) representing 24 phyla. Firmicutes, Proteobacteria, Bacteroidetes, Actinobacteria, and Tenericutes were the main components of the gut microbiota, with Proteobacteria and Firmicutes being the most abundant phyla (between 95.0 and 99.7% of all sequences) at all gut sites. Microbial communities changed in an age-dependent manner. Whereas, young birds had more Proteobacteria, Firmicutes, and Tenericutes dominated in older birds (>14 days old). In addition, 28 day old birds had more diverse bacterial communities than young birds. Furthermore, numerous significant differences in microbial profiles between the mucosa and luminal content of the small and large intestine were detected, with some species being strongly associated with the mucosa whereas others remained within the luminal content of the gut. Following oral infection of 14 day old broiler chickens with 1 × 108 CFU of C. jejuni NCTC 12744, it was found that C. jejuni heavily colonized throughout the small and large intestine. Moreover, C. jejuni colonization was associated with an alteration of the gut microbiota with infected birds having a significantly lower abundance of Escherichia (E.) coli at different gut sites. On the contrary, the level of Clostridium spp. was higher in infected birds compared with birds from the negative controls. In conclusion, the obtained results demonstrate how the bacterial microbiome composition changed within the early life of broiler chickens in the gut lumen and on the mucosal surface. Furthermore, our findings confirmed that the Campylobacter carrier state in chicken is characterized by multiple changes in the intestinal ecology within the host. |
p | Despite the importance of gut microbiota for broiler performance and health little is known about the composition of this ecosystem, its development and response towards bacterial infections. Therefore, the current study was conducted to address the composition and structure of the microbial community in broiler chickens in a longitudinal study from day 1 to day 28 of age in the gut content and on the mucosa. Additionally, the consequences of a Campylobacter (C.) jejuni infection on the microbial community were assessed. The composition of the gut microbiota was analyzed with 16S rRNA gene targeted Illumina MiSeq sequencing. Sequencing of 130 samples yielded 51,825,306 quality-controlled sequences, which clustered into 8285 operational taxonomic units (OTUs; 0.03 distance level) representing 24 phyla. Firmicutes, Proteobacteria, Bacteroidetes, Actinobacteria, and Tenericutes were the main components of the gut microbiota, with Proteobacteria and Firmicutes being the most abundant phyla (between 95.0 and 99.7% of all sequences) at all gut sites. Microbial communities changed in an age-dependent manner. Whereas, young birds had more Proteobacteria, Firmicutes, and Tenericutes dominated in older birds (>14 days old). In addition, 28 day old birds had more diverse bacterial communities than young birds. Furthermore, numerous significant differences in microbial profiles between the mucosa and luminal content of the small and large intestine were detected, with some species being strongly associated with the mucosa whereas others remained within the luminal content of the gut. Following oral infection of 14 day old broiler chickens with 1 × 108 CFU of C. jejuni NCTC 12744, it was found that C. jejuni heavily colonized throughout the small and large intestine. Moreover, C. jejuni colonization was associated with an alteration of the gut microbiota with infected birds having a significantly lower abundance of Escherichia (E.) coli at different gut sites. On the contrary, the level of Clostridium spp. was higher in infected birds compared with birds from the negative controls. In conclusion, the obtained results demonstrate how the bacterial microbiome composition changed within the early life of broiler chickens in the gut lumen and on the mucosal surface. Furthermore, our findings confirmed that the Campylobacter carrier state in chicken is characterized by multiple changes in the intestinal ecology within the host. |
body | Introduction A diverse microbiota is found throughout the gastrointestinal tract (GIT) of chickens, most predominant in the cecum (Mead, 1997; Videnska et al., 2014). The gut microbiota plays an essential role in nutrition, detoxification of certain compounds, growth performance and protection against pathogenic bacteria. The microbiota is crucial to strengthen the immune system, thereby affecting growth, health, and wellbeing of chicken. Generally, the gut microbiota modulates host responses to limit the colonization of pathogens (Rehman et al., 2007). There is little information about the diversity and function of the gut microbiota in chickens, its impact on the host and the impact of certain pathogens. Development of the gut microbiota in chickens occurs immediately after hatching and is influenced by both genetic and external factors like diet and environment (Apajalahti et al., 2004). It was reported that disturbances in the intestinal microbiota leads to a delay in growth, weakens the host resistance and increases the susceptibility to various infectious diseases (Lan et al., 2004). Gong et al. (2002) demonstrated that the cecal microbiota protects chickens against bacterial infections, while microbiota in the small intestine contributes significantly to its function, including digestion and nutrient absorption, which significantly determines the growth rate of the bird. Studies on gut microbiota have mostly been performed with chickens older than 1 week of age due to the various influences in day-old birds. However, the composition of gut microbiota at the first day of life in newly hatched chickens is a matter of interest within a longitudinal study. Therefore, the focus of the actual study was to determine the diversity and community structures of the microbiota within the small and large intestine from hatch until 4 weeks of age. Furthermore, differences among the mucosa-associated and luminal content microbiota were determined for the first time. Campylobacter (C.) jejuni is the most common cause of food-borne bacterial enteritis worldwide (EFSA, 2011). C. jejuni infection of chickens had previously not been considered to influence bird health and it was thought that C. jejuni is part of the normal microbiota of birds (EFSA, 2011). Understanding how Campylobacter species, especially C. jejuni, establishes successful colonization in chickens remains a foremost research priority as this gastrointestinal pathogen not only overcomes the host's defense system, but also competes with the microbial community for space and nutrients. It has been shown that Campylobacter requires numerous factors to successfully colonize the host, to translocate and to avoid clearance (Awad et al., 2014, 2015a,b, 2016; Humphrey et al., 2014). In addition, Awad et al. (2016) showed that Campylobacter had the ability to reduce butyrate, isobutyrate, valerate, and isovalerate which might be due to the utilization of short-chain fatty acids (SCFAs) as a carbon source (Masanta et al., 2013) or due to the reduction of butyric acid producing bacteria amongst the microbiota. In general, there is a complex interplay between microbiota composition and SCFAs concentration and it was found that the type and level of SCFAs in the gut can affect different members of the microbial community in various ways (Mon et al., 2015). It is still unknown how C. jejuni affects the ecology of the chicken gut, a feature of high importance considering a possible detrimental effect on the health of birds associated with C. jejuni colonization. Haag et al. (2012) demonstrated that C. jejuni colonization in mice depends on the microbiota of the host and vice versa and Campylobacter colonization induces a shift of the intestinal microbiota. Thus, it can be hypothesized that Campylobacter colonization is associated with an alteration in the intestinal microbiota of chickens as well. Therefore, the second aim of the actual study was to investigate the dynamics of an experimental Campylobacter jejuni NCTC 12744 infection in 14–28 days old chickens and the consequences on the alteration of the gut microbiome. Materials and methods Ethics statement The animal experiment was approved by the institutional ethics committee of the University of Veterinary Medicine and the Ministry of Research and Science under the license number GZ 68.205/0011-11/3b/2013. All husbandry practices were performed with full consideration of animal welfare. Experimental design In this study, a total of 45 1-day-old broiler chickens (males and females) were obtained from a commercial hatchery (Ross-308, Geflügelhof Schulz, Graz, Austria). Five day-old birds were immediately sacrificed for determining the gut microbiota of the jejunal and cecal mucosa. At 7 and 14 days of age, five birds were randomly selected for measuring the development of gut microbiota from gut content and mucosa. The birds were kept as non-infected for the first 2 weeks and were housed on wood shavings with feed and water supplied ad libitum. The birds were fed a standard commercial diet for the whole experimental period in order to avoid an influence of the change of diet on the microbial composition. At the first and 14 days of age birds were confirmed as Campylobacter-free by taking cloacal swabs which were streaked onto modified charcoal-cefaprazone-deoxycholate agar (CM0739, OXOID, Hampshire, UK) and grown for 48 h under microaerophilic conditions at 42°C. At 14 days of age, 15 birds were infected with Campylobacter jejuni (C. jejuni) reference strain NCTC 12744 and kept separately from 15 non-infected control birds which were inoculated with PBS only. C. jejuni was routinely grown in Lennox L Base broth (LB broth) (Invitrogen, California, USA) at 42°C for 48 h in a shaking incubator. Campylobacter colony-forming unit (CFU) was determined from each suspension by serial dilutions in duplicate using LB agar. Campylobacter suspensions were stored at −80°C by adding 2 mL of 40% glycerol/10 mL LB broth. For infection, Campylobacter suspensions were centrifuged for 5 min at 10,000 × rpm. The pellet was washed 3 times with phosphate-buffered saline (PBS) each time centrifuged at the same conditions as mentioned above. Finally, the pellets were resuspended in PBS and the necessary concentration was adjusted for birds' infection. The infection was performed orally via feeding tube (gavage) with a dose of 1 × 108 CFU/bird at 14 days of age as described previously (Awad et al., 2015a). At 7 days post infection 5 birds from each group were anesthetized by injection of a single dose of thiopental (20 mg/kg) into the wing vein and slaughtered by bleeding of the jugular vein. The final 10 birds/group were killed at 14 days post infection. At each time point the gastrointestinal content from the jejunum and ceca, as well as jejunal and cecal mucosa from 5 birds/group were taken to determine the gut microbiota. Intestinal segments were disclosed at the mesentery with sterile instruments and the digesta was removed. The luminal site of the intestinal segments was washed with sterile ice-cold PBS until the mucosa was completely cleaned from the digesta. The mucosa was rinsed several times with sterile ice cold PBS, after which the mucosa was collected aseptically by scraping off the mucosa using scalpel blades. All samples were stored at −80°C until further processing. DNA extraction, PCR amplification of the 16S rRNA gene, and illumina MISeq sequencing DNA from luminal content and gut mucosa samples was extracted using the PowerSoil® DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA, USA) as described previously (Mann et al., 2014; Yasuda et al., 2015). The same protocol of DNA extraction was applied to luminal content and gut mucosa. From each of the 130 samples a total of 250 mg of gut content or mucosa was used for DNA isolation according to manufacturer's instructions. DNA concentration was determined by a Qubit fluorometer (Invitrogen, Carlsbad, CA, USA). The V345 hypervariable region of the 16S rRNA genes was amplified with the primers F341 (5′-GTGYCAGCMGCCGCGGTAA-3′) (Zakrzewski et al., 2012) and R909 (5′-CCGYCAATTYMTTTRAGTTT-3′) (Tamaki et al., 2011). An amplicon size of approximately 568 bp was produced. 16S rRNA gene PCRs, library preparation and sequencing were performed by Microsynth (Microsynth AG, Balgach Switzerland). Libraries were constructed by ligating sequencing adapters and indices onto purified PCR products using the Nextera XT Sample Preparation Kit (Illumina) and equimolar amounts of each of the libraries were pooled and sequenced on an Illumina MiSeq Sequencing Platform. Sequence data were analyzed with the software package QIIME (Caporaso et al., 2010). Low quality sequences (q < 20) were filtered, chimeric sequences were excluded by using the USEARCH 6.1 database (Edgar, 2010) and sequences were clustered into operational taxonomic units (OTUs; 97% similarity) with the QIIME script “pick_open_reference_otus.py.” OTUs with less than 10 sequences were removed, resulting in 8285 OTUs, which were used for all downstream analysis. The representative sequences of the 50 most abundant OTUs over all sampling time points were classified against type strains using the Greengenes database (http://greengenes.lbl.gov) (DeSantis et al., 2006). Microbial diversity analysis Both alpha and beta diversity indices were used to estimate the microbiome diversity within—and between microbial communities. Calculations were done with the “summary.single” command in the software package mothur (http://www.mothur.org/; Kozich et al., 2013). Alpha diversity indices analysis included Chao1 index (richness estimate), abundance-based coverage estimator (ACE, richness estimate), Shannon's diversity, and Simpson's diversity index. For the Bray-Curtis similarity, the dataset was rarefied to the minimum number of sequences per sample. Rarefaction curve was constructed based on the observed number of OTUs and nearly reached asymptotes for all samples (data not shown). Principal component analysis was done with JMP® (Version 10.0.0, SAS Institute Inc., Cary, NC). Shared OTUs among gut sites at different age were plotted as Venn diagrams using the R environment (package “VennDiagram,” version 1.6.17.) (Chen, 2016). Heatmaps were created using JColorGrid (Joachimiak et al., 2006). Statistical analysis Statistically significant differences in relative abundance with regard to sampling sites and time were calculated using “metastats” in mothur, which is based on the homonymous bioinformatics program (White et al., 2009; Paulson et al., 2011). “Metastats” uses repeated t statistics and Fisher's tests on random permutations to handle sparsely-sampled features (White et al., 2009). Results were reported as a mean and standard deviation (SD). The significance level was set to P < 0.05. The P-values were adjusted with the Benjamini and Hochberg false discovery rate correction (FDR, q-value), and a q < 0.25 was considered significant (Lim et al., 2016). Furthermore, significant differences between the diversity estimators of the two groups were performed using the non-parametric Kruskal-Wallis-test followed by Mann-Whitney-test. PASW statistics 20, SPSS software (Chicago, Il., USA) was used for statistical analyses of diversity estimators. Accession numbers Sequencing data are available in the European Nucleotide Archive (ENA) database under the accession number PRJEB14860. Results Sequence analysis, phylum and OTU classification Sequencing of 130 samples yielded 51,825,306 quality-controlled sequences, clustering into 8285 operational taxonomic units (OTUs; 0.03 distance level). Throughout all gut sites 24 phyla were identified with Firmicutes, Proteobacteria, and Tenericutes being the most abundant ones. In Figure S1A, Tables S1A–D, relative abundances of all phyla are delineated with respect to age and groups. The results showed that in the jejunum and cecum, Firmicutes and Proteobacteria were the dominating luminal and mucosal-associated phyla in all birds investigated (Tables S2, S3). At the first day of life Proteobacteria were significantly higher in the jejunal (P = 0.0000, q = 0.0000) and cecal (P = 0.016; q = 0.059) mucosa of the birds and decreased thereafter, as no significant differences were found between samples from day 14 to day 28 of age (P = 0.140; q = 0.438 and P = 0.519; q = 0.955). On the contrary, Firmicutes were significantly lower at day 1 and increased thereafter (P = 0.001; q = 0.016 and P = 0.006; q = 0.055 in the jejunal and cecal mucosa, respectively). For infected birds, relative abundances of bacterial phyla at the two sampling time points carried out post infection are represented in Figure S1B, Tables S4A–D. Figure 1 shows that the phylum Proteobacteria decreased while Firmicutes increased at either 21 (7 dpi) or 28 days of age (14 dpi). There was a significant decrease in Actinobacteria and Proteobacteria in the jejunal mucosa at 14 dpi (P = 0.006; q = 0.100 and P = 0.005; q = 0.100), while Firmicutes and Bacteroidetes were more abundant in the infected birds compared to the controls (P = 0.005; q = 0.100 and P = 0.023; q = 0.217, Table S4A). However, in the cecal content and cecal mucosa, Bacteroidetes (P = 0.001; q = 0.019) increased at 7 dpi, but decreased (P = 0.002; q = 0.026 and P = 0.005; q = 0.048) at 14 dpi in the infected birds compared with the controls, indicating that the Campylobacter infection modulates the jejunal and cecal phylum abundances in different ways. Figure 1 Relative abundances (%) of the most abundant phyla in the infected birds compared with the controls at the two sampling points post infection of (A) jejunum and (B) cecum. Data are presented as the mean values and standard deviation (SD). JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i). In Table 1, the 50 most abundant OTUs from all birds are listed including the internal OTU number, relative abundance together with the reference strain and similarity (compared with strains of the Greengenes database). Relative OTUs abundances at different ages in all birds are shown in Tables S5A–D, S6A–D. The OTUs and species abundances sorted by age at the four gut sites of the birds are shown in the heatmaps of Figure S2. In total, the 50 most abundant OTUs accounted for 73.9% of all sequences and of those 42 OTUs differed significantly in their relative abundances over all gut sites independent of the age (Tables 2, 3). At the first day of age, a notable high relative abundance of OTU 1, 25, 27, and 35 (best type strain hits: Escherichia coli, Enterococcus faecalis, Clostridium paraputrificum, and Clostridium sartagoforme) were found in both jejunal and cecal mucosa (Tables S5A,C), whereas OTU 38 (best type strain hit: Acinetobacter johnsonii) was only abundant in the jejunal mucosa and OTU 42 (best type strain hit: C. paraputrificum) was only abundant in the cecal mucosa. All these abundant OTUs decreased by age. In the jejunal mucosa, OTU 1 was the most abundant (57.9%), followed by the other four OTUs which ranged between 2.6 and 7.9%. Similarly, in the mucosa of the cecum, OTU 1 was highly abundant (65.9%), followed by OTUs 27, 25, 35, and 42 which ranged between 7.8 and 3.3%. Table 1 The 50 most abundant OTUs retrieved from different gut sites from all birds independent of the infection status. OTUs No. of sequences Relative abundance (%) Best type strain hita Similarity (%) OTU 1 642068 10.64 Escherichia coli (GU968184.1) 100 OTU 2 341923 5.66 Lactobacillus johnsonii (HM772969.1) 100 OTU 3 339288 5.62 Lactobacillus salivarius (NZ_AEBA01000145.1) 100 OTU 4 310060 5.14 Clostridium spp. (FJ808599.1) 87 OTU 5 273783 4.54 Enterococcus durans (FJ917726.1) 100 OTU 6 209121 3.46 Anaerotruncus colihominis (NR_027558.1) 100 OTU 7 208070 3.45 Eubacterium desmolans (L34618.1) 98 OTU 8 161864 2.68 Clostridium cellulolyticum (X71847.1) 87 OTU 9 157466 2.61 Spiroplasma lampyridicola (AY189134.1) 82 OTU 10 151864 2.52 Clostridium leptum (AJ305238.1) 97 OTU 11 130587 2.16 Eubacterium desmolans (L34618.1) 99 OTU 12 127446 2.11 Eubacterium desmolans (L34618.1) 98 OTU 13 120732 2.00 Clostridium papyrosolvens (NR_026102.1) 87 OTU 14 113436 1.88 Eubacterium coprostanoligenes (HM037995.1) 92 OTU 15 98491 1.63 Clostridium straminisolvens (NR_024829.1); Clostridium thermocellum (AB558166.1) 87 OTU 16 87863 1.46 Clostridium cellulolyticum (NC_011898.1) 87 OTU 17 70842 1.17 Bacillus subtilis (FJ608705.1) 94 OTU 18 67038 1.11 Lactobacillus reuteri (EU547311.1) 99 OTU 19 66212 1.10 Ruminococcus bromii (NR_025930.1) 94 OTU 20 65592 1.09 Eubacterium desmolans (L34618.1) 95 OTU 21 53133 0.88 Clostridium cellulolyticum (NC_011898.1); Clostridium papyrosolvens (NR_026102.1) 87 OTU 22 49736 0.82 Clostridium thermocellum (AB558166.1) 85 OTU 23 47570 0.79 Clostridium thermosuccinogenes (Y18180.1); Clostridium thermocellum (AB558166.1) 86 OTU 24 40373 0.67 Clostridium leptum (AJ305238.1) 95 OTU 25 36925 0.61 Enterococcus faecalis (FJ607291.1) 100 OTU 26 35311 0.58 Proteus mirabilis (GU477712.1) 100 OTU 27 31154 0.52 Clostridium paraputrificum (AY442815.1) 100 OTU 28 29186 0.48 Variovorax paradoxus (HQ005421.1) 100 OTU 29 28876 0.48 Campylobacter subsp. jejuni (NC_008787.1) 100 OTU 30 27988 0.46 Clostridium leptum (AJ305238.1) 93 OTU 31 23587 0.39 Anaerotruncus colihominis (NR_027558.1) 93 OTU 32 23559 0.39 Lactobacillus crispatus (FN692037.1) 100 OTU 33 22863 0.38 Phyllobacterium myrsinacearum (AY785330.1) 100 OTU 34 21547 0.36 Catabacter hongkongensis (AY574991.1); Clostridium thermosuccinogenes (Y18180.1) 86 OTU 35 20378 0.34 Clostridium sartagoforme (FJ384380.1) 100 OTU 36 18849 0.31 Acetivibrio cellulolyticus (L35515.1) 95 OTU 37 18055 0.30 Clostridium papyrosolvens (NR_026102.1) 86 OTU 38 17890 0.30 Acinetobacter johnsonii (EU977694.1) 100 OTU 39 15658 0.26 Clostridium papyrosolvens (NR_026102.1) 87 OTU 40 15361 0.25 Lactobacillus johnsonii (EU381128.1) 96 OTU 41 15143 0.25 Clostridium thermosuccinogenes (Y18180.1) 87 OTU 42 14985 0.25 Clostridium paraputrificum (AY442815.1) 100 OTU 43 14682 0.24 Marinobacter sp. (FJ889664.1) 99 OTU 44 14652 0.24 Clostridium papyrosolvens (NR_026102.1) 87 OTU 45 14304 0.24 Shigella flexneri (CP000266.1) 99 OTU 46 13619 0.23 Clostridium cellulolyticum (NC_011898.1) 86 OTU 47 13307 0.22 Clostridium papyrosolvens (NR_026102.1) 86 OTU 48 13152 0.22 Clostridium papyrosolvens (NR_026102.1) 87 OTU 49 12978 0.21 Clostridium papyrosolvens (NR_026102.1) 87 OTU 50 12418 0.21 Lactobacillus salivarius (NZ_AEBA01000145.1) 98 a Greengenes best type strain hit accession numbers are listed in parenthesis. Table 2 Relative abundances (%) of the most abundant OTUs in different gut sites of control birds (day 1–28). OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa OTU 49 0 0.02 0.05 0.11 0.01 0.02 0.01 0.02 0.056 0.164 0.655 0.858 0.366 0.623 0.133 0.326 OTU 25 1.89 4.01 0.06 0.07 1.05 2.95 0.01 0.02 0.001 0.011 0.015 0.067 0.365 0.623 0.001 0.011 OTU 5 12.41 25.84 13.09 21.85 0.28 0.56 0.07 0.09 0.920 0.990 0.039 0.134 0.002 0.017 0.001 0.011 OTU 30 0.45 1.45 0.40 0.72 0.74 1.11 1.25 2.09 0.913 0.990 0.385 0.643 0.808 0.946 0.059 0.170 OTU 9 0.90 2.72 1.03 3.05 3.56 9.78 5.82 15.04 0.938 0.990 0.514 0.765 0.196 0.401 0.091 0.244 OTU 13 1.34 5.22 0.75 1.84 1.36 4.51 1.41 4.43 0.714 0.890 0.831 0.946 0.940 0.990 0.549 0.770 OTU 15 0.07 0.20 0.13 0.32 1.17 1.98 4.21 9.38 0.792 0.942 0.095 0.250 0.005 0.030 0.001 0.011 OTU 18 2.36 8.46 2.34 6.03 0.08 0.23 0.03 0.09 0.961 0.994 0.409 0.665 0.081 0.220 0.013 0.059 OTU 21 0.65 2.01 0.32 0.87 0.53 1.11 1.08 3.21 0.588 0.787 0.599 0.796 0.812 0.946 0.294 0.526 OTU 33 0.96 1.38 2.57 5.92 0 0 0 0 0.341 0.603 0.001 0.011 OTU 12 0.95 2.20 1.25 4.71 2.42 5.21 5.41 11.82 0.776 0.929 0.285 0.519 0.491 0.739 0.131 0.326 OTU 28 3.21 7.19 2.99 7.77 0 0 0 0 0.941 0.990 0.006 0.034 0.001 0.011 0.001 0.011 OTU 37 0.12 0.56 0 0.01 0.39 1.93 0.07 0.28 0.140 0.326 0.939 0.990 0.947 0.991 0.177 0.379 OTU 40 0.05 0.11 1.08 1.53 0 0 0.10 0.44 0.001 0.011 0.464 0.722 0.001 0.011 0.008 0.043 OTU 3 10.36 20.66 18.43 23.28 0.39 0.63 1.52 5.30 0.252 0.475 0.517 0.765 0.001 0.011 0.002 0.017 OTU 26 0.03 0.07 0.03 0.06 1.34 2.35 1.75 3.25 0.483 0.737 0.691 0.875 0.001 0.011 0.003 0.020 OTU 19 0.80 1.99 0.22 0.57 1.09 2.22 1.01 2.17 0.189 0.395 0.979 0.997 0.961 0.994 0.134 0.326 OTU 44 0.04 0.15 0.02 0.04 0.06 0.12 0.07 0.14 0.748 0.908 0.660 0.858 0.452 0.715 0.052 0.155 OTU 39 0.02 0.07 0.01 0.02 0.07 0.20 0.08 0.19 0.769 0.927 0.726 0.893 0.253 0.475 0.046 0.147 OTU 29 0 0 0 0 0 0 0 0 0.002 0.017 OTU 2 10.86 14.76 24.38 24.19 0.13 0.26 0.31 1.13 0.046 0.147 0.817 0.946 0.001 0.011 0.001 0.011 OTU 38 1.51 5.31 0.17 0.67 0 0 0 0 0.145 0.326 0.002 0.017 OTU 42 0.51 1.20 0.01 0.03 0.67 1.71 0.01 0.03 0.012 0.057 0.041 0.136 0.717 0.890 0.669 0.864 OTU 17 0.46 1.30 0.02 0.05 2.79 7.57 0.05 0.15 0.041 0.136 0.063 0.176 0.243 0.466 0.571 0.770 OTU 1 14.87 24.08 5.33 7.93 22.17 26.59 13.03 17.69 0.069 0.190 0.231 0.452 0.295 0.526 0.062 0.176 OTU 11 0.69 1.32 0.51 0.97 2.63 7.62 3.10 5.11 0.362 0.623 0.692 0.875 0.458 0.719 0.003 0.020 OTU 4 0.51 2.00 0.17 0.56 1.34 4.60 2.14 7.58 0.571 0.770 0.611 0.806 0.525 0.770 0.147 0.326 OTU 48 0 0 0 0 0 0 0 0 0.036 0.131 OTU 14 0.24 0.69 0.22 0.43 3.77 8.30 4.66 10.97 0.542 0.770 0.747 0.908 0.023 0.091 0.004 0.025 OTU 46 0 0.02 0.01 0.02 0.26 0.65 0.25 0.50 0.348 0.609 0.991 1.000 0.028 0.106 0.039 0.134 OTU 31 0.23 0.55 0.05 0.12 0.87 1.67 0.33 0.51 0.137 0.326 0.170 0.368 0.166 0.364 0.016 0.068 OTU 45 0.05 0.09 0.01 0.01 0.35 0.56 1.02 1.62 0.023 0.091 0.096 0.250 0.016 0.068 0.004 0.025 OTU 10 0.37 1.03 0.20 0.46 4.39 11.22 4.97 10.40 0.477 0.736 0.824 0.946 0.013 0.059 0.003 0.020 OTU 32 0.12 0.43 0.23 0.79 0 0 0 0 0.540 0.770 0.868 0.975 0.012 0.057 0.006 0.034 OTU 8 0.28 1.29 0.03 0.10 1.43 5.01 2.34 7.10 0.537 0.770 0.551 0.770 0.370 0.624 0.138 0.326 OTU 6 1.17 3.54 0.13 0.28 9.20 15.81 1.39 1.56 0.238 0.461 0.007 0.039 0.021 0.087 0.001 0.011 OTU 36 0.03 0.11 0.11 0.22 0.68 1.66 0.25 0.49 0.144 0.326 0.263 0.488 0.003 0.020 0.220 0.445 OTU 35 0.57 1.28 0.02 0.04 0.90 2.13 0.02 0.08 0.012 0.057 0.034 0.126 0.542 0.770 0.867 0.975 OTU 7 1.07 2.73 1.41 2.66 3.52 7.28 6.47 12.19 0.832 0.946 0.282 0.518 0.125 0.320 0.037 0.132 OTU 16 0.73 3.50 0.27 1.01 1.41 3.77 1.96 4.92 0.905 0.990 0.562 0.770 0.400 0.656 0.146 0.326 OTU 27 0.98 2.31 0.02 0.07 1.56 4.02 0.01 0.05 0.012 0.057 0.048 0.151 0.563 0.770 0.719 0.890 OTU 20 1.68 4.52 0.05 0.18 0.86 4.28 0.91 4.07 0.049 0.151 0.981 0.997 0.448 0.715 0.997 1.000 OTU 50 0.09 0.15 0.84 0.95 0 0.01 0.06 0.23 0.001 0.011 0.486 0.737 0.001 0.011 0.002 0.017 OTU 22 0 0 0 0.02 0 0 0 0.01 0.231 0.452 0.882 0.985 OTU 47 0.12 0.53 0 0.02 0.32 1.55 0.06 0.22 0.191 0.395 0.917 0.990 0.933 0.990 0.180 0.381 OTU 41 0 0.01 0 0 0 0 0 0 0.228 0.452 1.000 1.000 OTU 23 0.12 0.50 0.01 0.02 0.07 0.20 0.09 0.23 0.136 0.326 0.682 0.874 0.819 0.946 0.024 0.093 OTU 43 0.01 0.03 0 0 0 0 0 0 OTU 34 0.03 0.14 0 0 0.06 0.16 0.14 0.38 0.903 0.990 0.417 0.672 0.390 0.645 0.051 0.155 OTU 24 0.11 0.52 0.18 0.39 1.18 1.89 1.10 1.90 0.567 0.770 0.973 0.997 0.001 0.011 0.003 0.020 a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. Table 3 Relative abundances (%) of the most abundant OTUs in different gut sites of infected birds (days 21 and 28). OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa OTU 49 0.18 0.28 0.43 0.98 0.61 1.44 0.52 0.91 0.689 0.880 0.936 0.989 0.550 0.791 0.516 0.776 OTU 25 0.02 0.04 0.08 0.09 0.00 0.00 0 0 0.077 0.178 0.063 0.168 OTU 5 1.65 2.21 8.89 6.18 0.01 0.01 0 0 0.009 0.043 0.761 0.927 0.001 0.007 0.001 0.007 OTU 30 0.31 0.94 0.06 0.08 0.30 0.38 0.16 0.12 0.957 0.989 0.355 0.596 1.000 1.000 0.013 0.056 OTU 9 0.17 0.39 0.14 0.14 1.47 4.29 2.06 5.88 0.903 0.987 0.575 0.791 0.530 0.785 0.217 0.408 OTU 13 0.64 1.06 0.72 1.35 2.87 3.77 2.65 2.58 0.955 0.989 0.950 0.989 0.056 0.159 0.020 0.071 OTU 15 0.08 0.13 0.01 0.02 1.24 0.89 2.13 1.23 0.049 0.146 0.040 0.126 0.001 0.007 0.001 0.007 OTU 18 4.67 9.39 6.34 11.77 0.19 0.44 0.14 0.36 0.572 0.791 0.857 0.986 0.102 0.218 0.011 0.051 OTU 21 0.28 0.58 0.16 0.19 1.63 2.60 1.93 2.41 0.565 0.791 0.611 0.611 0.085 0.191 0.009 0.043 OTU 33 1.11 1.14 0.13 0.13 0.00 0.00 0.00 0.00 0.008 0.041 1.000 1.000 0.001 0.007 0.001 0.007 OTU 12 0.51 0.74 0.06 0.08 0.06 0.09 0.05 0.05 0.056 0.159 0.929 0.989 0.062 0.168 0.796 0.949 OTU 28 1.19 1.20 0.20 0.21 0.00 0.00 0.00 0.00 0.015 0.060 0.016 0.060 0.001 0.007 0.001 0.007 OTU 37 0.14 0.27 0.01 0.02 0.35 0.18 0.51 0.27 0.074 0.178 0.077 0.178 0.207 0.394 0.001 0.007 OTU 40 0.07 0.08 1.35 0.83 0.01 0.01 0.00 0.01 0.001 0.007 0.881 0.987 0.008 0.041 0.001 0.007 OTU 3 11.02 13.33 29.61 19.69 0.52 0.56 0.41 0.45 0.067 0.173 0.865 0.986 0.004 0.023 0.001 0.007 OTU 26 0 0 0.01 0.05 0.01 0.01 0.01 0.01 0.542 0.791 0.801 0.949 0.070 0.176 0.990 1.000 OTU 19 0.14 0.29 0.31 0.24 3.24 7.48 2.09 5.77 0.372 0.613 0.614 0.823 0.107 0.223 0.441 0.700 OTU 44 0.43 1.20 0.07 0.12 0.49 0.94 1.06 2.17 0.594 0.809 0.574 0.791 0.552 0.791 0.014 0.059 OTU 39 0.02 0.05 0.13 0.20 0.59 0.79 1.02 1.34 0.072 0.178 0.318 0.539 0.001 0.007 0.016 0.060 OTU 29 0.30 0.66 0.01 0.03 3.92 6.25 0.38 0.51 0.052 0.152 0.049 0.146 0.036 0.115 0.005 0.028 OTU 2 19.98 22.32 23.46 10.10 0.85 1.46 0.19 0.30 0.834 0.975 0.285 0.493 0.002 0.012 0.001 0.007 OTU 38 0 0.01 0 0 0 0 0 0 0.690 0.012 OTU 42 0 0 0 0 0 0 0 0 OTU 17 0.62 1.33 0.25 0.31 4.45 6.58 0.12 0.18 0.451 0.703 0.002 0.012 0.091 0.201 0.531 0.785 OTU 1 0.11 0.18 0.81 1.36 0.28 0.40 0.19 0.36 0.145 0.292 0.760 0.927 0.280 0.491 0.255 0.455 OTU 11 1.09 1.39 0.10 0.10 2.01 2.44 2.31 3.56 0.026 0.086 0.761 0.927 0.907 0.987 0.007 0.038 OTU 4 3.43 6.60 0.13 0.11 12.51 8.03 16.82 10.92 0.154 0.303 0.162 0.315 0.016 0.060 0.001 0.007 OTU 48 0.41 1.14 0.01 0.02 2.29 7.23 0.38 1.17 0.225 0.414 0.747 0.927 0.817 0.962 0.222 0.413 OTU 14 0.24 0.65 0.07 0.07 0.45 0.84 1.41 2.08 0.364 0.606 0.122 0.251 0.619 0.824 0.076 0.178 OTU 46 0.21 0.60 0.01 0.02 0.49 0.81 0.52 0.87 0.306 0.524 0.757 0.927 0.396 0.646 0.016 0.060 OTU 31 0.03 0.06 0.03 0.04 0.37 0.52 0.08 0.07 0.955 0.989 0.057 0.159 0.012 0.055 0.019 0.068 OTU 45 0 0 0 0 0 0 0 0 1.000 1.000 0.281 0.491 OTU 10 0.26 0.82 0.09 0.12 0.29 0.57 0.22 0.30 0.960 0.989 0.896 0.987 0.891 0.987 0.175 0.336 OTU 32 2.90 3.72 3.80 3.98 0.18 0.46 0.05 0.11 0.872 0.986 0.567 0.791 0.004 0.023 0.001 0.007 OTU 8 1.21 2.88 0.05 0.09 7.75 7.99 6.25 8.70 0.036 0.115 0.917 0.989 0.021 0.073 0.001 0.007 OTU 6 0.82 1.99 0.10 0.13 4.11 2.46 1.24 1.97 0.455 0.703 0.026 0.086 0.019 0.068 0.001 0.007 OTU 36 0.21 0.40 0.23 0.21 0.34 0.37 0.19 0.22 0.893 0.987 0.441 0.700 0.473 0.724 0.871 0.986 OTU 35 0 0 0 0 0 0 0 0 OTU 7 0.24 0.40 0.08 0.17 4.65 13.62 6.23 18.65 0.095 0.205 0.692 0.880 0.501 0.760 0.062 0.168 OTU 16 0.19 0.27 0.29 0.47 1.37 1.80 1.55 1.94 0.776 0.932 0.653 0.862 0.074 0.178 0.048 0.146 OTU 27 0 0 0 0 0 0 0 0 OTU 20 0.22 0.67 0.03 0.05 4.32 13.62 0.62 1.88 0.849 0.986 0.770 0.932 0.576 0.791 0.424 0.686 OTU 50 0.10 0.17 1.20 0.73 0.01 0.01 0.01 0.01 0.001 0.007 0.979 1.000 0.013 0.056 0.001 0.007 OTU 22 0.14 0.42 0 0 2.08 5.32 3.60 9.82 0.107 0.223 0.671 0.877 0.236 0.430 0.001 0.007 OTU 47 0.03 0.06 0.01 0.01 0.20 0.10 0.31 0.23 0.244 0.440 0.092 0.201 0.001 0.007 0.001 0.007 OTU 41 0.99 2.99 0 0 0.50 0.87 1.28 3.32 0.723 0.913 0.923 0.989 OTU 23 0.63 1.18 0.02 0.02 2.39 2.31 2.88 2.65 0.124 0.252 0.448 0.703 0.064 0.168 0.001 0.007 OTU 43 8.90 28.14 0 0 0 0 0 0 OTU 34 0.02 0.05 0 0 0.85 0.79 1.54 1.09 0.148 0.294 0.068 0.173 0.001 0.007 0.001 0.007 OTU 24 0 0 0.05 0.07 0.15 0.13 0.12 0.11 0.674 0.877 0.082 0.187 a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. The OTUs and species abundances sorted by gut sites of the infected birds compared with the control birds are shown in the heatmaps (Figure 2). Interestingly, in the infected birds, the abundance of E. coli and Eubacterium desmolans (best type strain hits) were lower at different gut sites (Figure 3A). On the contrary, Clostridium spp. abundance was higher in the infected birds compared with the negative controls (Figure 3B). Figure 2 Heatmap showing the relative abundances (%) of the 50 most-abundant OTUs sorted by gut sites of the infected birds compared with the controls at the two sampling points post infection. The heat map integrates relative abundance of a given phylotype. Colour scaling is ranged from 0 to ≥ 25%. n.d, not detected. Figure 3 Relative abundances (%) of the most relevant OTUs in the infected birds compared with the controls at the two sampling points post infection (A) OTUs 1 and 12, (B) OTUs 4 and 29. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. Assessment of the microbial community diversity Diversity indices estimating species richness and evenness for birds are shown in Figure 4. Diversity indices indicated that microbial richness and diversity increased with age. Interestingly, diversity indices were not different comparing samples from days 1 and 7. However, older chickens (14–28 days of age) had a significantly more diverse microbial community structure as indicated by the number of OTUs observed (Sobs), Chao1, ACE, Shannon's index, and Simpson index (P < 0.01). In addition, the microbial diversity in older chickens is more consistent, as there was no difference in diversity indices comparing samples from days 14 to 28. The results also revealed significant differences in the microbial diversity among jejunum and cecum as the chicken aged, supported by Sobs (P < 0.001), Chao1 (P < 0.001), ACE (P < 0.001), Shannon's index (P < 0.001), and Simpson index (P = 0.060) with a more complex diversity in the cecum compared with the jejunum. Furthermore, a difference in species richness among the luminal and mucosa-associated gut microbiota, independent of the age, was detected in all birds as supported by Sobs (P = 0.017), Chao1 (P = 0.015), ACE (P = 0.022), respectively. Figure 4 Species richness and diversity measures of the microbial community at all gut sites in the control (A), infected birds (B), and (C) species richness and diversity estimates for bacteria from cecum content of the infected birds compared with the controls. Left Y-axis for number of observed OTUs (Sobs), Chao 1 and ACE, and Right Y-axis for Shannon and Simpson. Significant differences were calculated with Kruskal-Wallis-tests and Mann-Whitney-tests, and significance was declared at P < 0.05. Data are presented as the mean values and SD. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. In the infected birds, significant differences in the microbial diversity among jejunum and cecum supported by Sobs (P < 0.001), Chao1 (P < 0.001), ACE (P < 0.001), Shannon's index (P < 0.001), and Simpson index (P = 0.011) were found. Additionally, an increase in the species richness among luminal and mucosa-associated gut microbiota of the infected birds at 14 dpi compared with those from 7 dpi was obtained. Diversity indices were not significantly different among the gut sites of infected and control birds. Exceptional to this, a higher species richness was noticed in the cecum content of infected birds at 14 dpi, supported by Sobs, Chao1, and ACE (P = 0.047, Figure 4C), indicating that the Campylobacter infection increased the microbiota complexity. Similarity and stability of the gut microbiota composition over time The microbial community similarity among all samples over time was assessed by calculating a Bray-Curtis similarity matrix. Community similarity analysis based on the Bray-Curtis index showed clear differences between gut sites and age, indicating strong shifts in microbial community structures (Figure 5). In addition, the Bray-Curtis index suggested that the birds at the first day of age displayed a high degree of dissimilarity compared with the other ages. It was also apparent that microbiota compositions of older birds were more similar compared with young birds. Figure 5 Microbial community similarity between all samples calculated with Bray-Curtis similarities, which displays the similarity results between the control and infected groups according to age and gut sites. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. The Bray-Curtis index revealed clear differences between jejunum and cecum from infected birds at the two sampling time points post infection. Furthermore, the comparison of the microbiota between control and infected birds showed that community structures were more dissimilar at the OTUs level, demonstrating that the gut microbial communities changed as a result of infection. To measure the similarity between microbial communities in all birds at different ages, principal component analysis (PCA) was performed (Figure 6). PCA analysis showed that there was a clear clustering of the birds at days 1 and 7 of age in the jejunum and cecum compared with the other days. In addition, the microbial community of the older chickens clustered with less variation compared to young birds. PCA plots also demonstrate that, the microbial community was more separated in the ceca than in the jejunum. Figure 6 Principal component analysis (PCA) was analyzed for the control (A) and infected birds (B). Orange (day 1), Red (day 7), Green (day 14), Blue (day 21), and Black (day 28). Each symbol indicates an individual bird. All PCA plots include the data of all samples; symbols not belonging to the sample group indicated in the header are displayed faded. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. To delineate the shared species among the groups, a Venn diagram displaying the overlaps between gut sites at different ages and groups was performed (Figure S3). The proportions of shared OTUs appear to be low at each gut site from day 1 to day 28 of age. These shared species, however, varied from one site to another. Furthermore, the analysis showed that only 399 OTUs (n = 1847 OTUs) were shared among the jejunal mucosa in the control and infected birds, while 745 OTUs (n = 2401 OTUs) were shared between the jejunal content in the control and infected birds at the two time points post infection (Figure 7A). In the cecal mucosa and the cecal content, the comparison revealed that only 2218 OTUs (n = 6736 OTUs) and 2617 OTUs (n = 6860 OTUs) were shared, among control and infected birds combining the two time points post infection (Figure 7B). These data demonstrated that 25–36% of the observed OTUs in the jejunum and cecum were shared between the control and infected birds, respectively. Figure 7 Venn diagrams showing the shared OTUs between the control and infected birds at different gut sites at the two sampling points post infection (A) jejunum; (B) cecum. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i); d, day. Discussion The intestinal microbiota acts as a physical barrier for incoming pathogens and plays an important role in the host resistance against infections by both direct interactions with pathogenic bacteria via competitive exclusion, such as occupation of attachment sites or consumption of nutrient sources, and indirectly by influencing the immune system via production of antimicrobial substances (Sekirov et al., 2010). Development of the gut microbiota in chickens occurs immediately after hatching and by getting older, this microbiome becomes very diverse until it reaches a relatively stable dynamic state (Pan and Yu, 2014). Interactions of the intestinal microbiome with the host and certain microorganisms have profound effects on bird health, and are therefore of great importance for poultry production. Consequently, in the present study, the composition of the gut microbiota of chickens in a longitudinal study from day 1 to day 28 of age was analyzed and the differences between content and mucosa-associated gut microbiota were investigated. In order to extend the range of analyses comparisons were performed between control chickens and chickens infected at 14 days of age with C. jejuni. In this study, a high diversity of phyla (15 in the jejunal and 4 in the cecal mucosal samples) was found at day 1 of life, indicating a rapid intake of environmental organisms after birth. In addition, the composition of the gut microbiota differed substantially between young and older birds, with Proteobacteria being significantly more present at the first day of life and decreasing thereafter, whereas the Firmicutes were the predominant phylum in older birds. This is in agreement with Lu et al. (2003) who found that the gut is firstly colonized by the phylum Proteobacteria, particularly by the family Enterobacteriaceae. In older birds, the phylum Firmicutes mainly represented by Lachnospiraceae, Ruminococcaceae, Clostridiaceae, and Lactobacillaceae dominated. As a consequence, the chicken gut is firstly colonized by facultative aerobes which are substituted later on by anaerobes. Obviously, oxygen consumption by the aerobic bacteria alters the gut ecosystem toward more reducing conditions, which facilitates subsequent growth and colonization of the obligate anaerobes (Wise and Siragusa, 2007). Besides Proteobacteria and Firmicutes, also lower abundant phyla (e.g., Actinobacteria and Tenericutes) changed significantly with time, indicating high dynamics in the re-organization of the whole microbiome through time. Taken together, the present study revealed that the chicken gut is largely dominated by the phyla Proteobacteria and Firmicutes, with lower proportions of Actinobacteria, Bacteroidetes, and Tenericutes. Similarly, previous studies have also shown that Firmicutes, Bacterioidetes, and Proteobacteria are the most common phyla in the chicken ceca (Wei et al., 2013; Oakley et al., 2014; Sergeant et al., 2014). Interestingly, jejunal, and cecal microbiota were found to be distinct and certain acid-tolerant bacteria, mostly Acidobacteria, were present in the jejunum only. Altogether, the results demonstrated that the abundance of bacteria varied between the jejunum and the cecum, with some species more present in the jejunum (e.g., Acinetobacter and Acidobacteria) and others (e.g., Bacteroides and Clostridium) being predominant in the cecum of chickens. This and other variations can be explained by the fact that feed passes quickly through the foregut and is retained for hours in the hindgut. In addition, the small intestine is mainly responsible for food digestion and absorption, while the large intestine, especially the cecum, is responsible for microbial fermentation, further nutrient absorption and detoxification of substances that are harmful to the host (Gong et al., 2002). Chickens investigated in the current study had a high abundance of E. coli and E. faecalis (best type strain hits) in the first week of life which might potentially increase their resistance to other bacterial infections. E. coli, a facultative anaerobe bacterium, was the dominant species in the early life of chickens. Thus, a depletion of E. coli during the second week of life could potentially affect the host susceptibility to enteric pathogen infections, representing a key role for these gut microbiota in host resistance. This decrease in E. coli abundance has been attributed with a beginning dominance of anaerobes (Zhu and Joerger, 2003). It may be possible that such disturbances in the community structure allow a pathogen to colonize and proliferate. Anyhow, it remains hypothetical whether these diversity changes influence the susceptibility to pathogens and the outcome of infection. The current results revealed that E. coli, E. faecalis, C. paraputrificum, and C. sartagoforme (best type strain hits) were more predominant in the mucosa than in the lumen, suggesting significant implications for birds' health, considering that the mucosa-associated bacteria are of great importance in the host mucosal responses with consequences for the mucosal barrier (Ott et al., 2004). Despite the high prevalence of Campylobacter in chickens the mechanism of colonization in the gut is still poorly understood. The high bacterial load in the gut and the establishment of a latent infection characterized by continuous shedding indicates that Campylobacter in chickens can modify the microbiota composition. In the current study it could be shown that Campylobacter colonization shifted the two major phyla towards an enrichment of Firmicutes with concomitant reduction of Proteobacteria. Interestingly, a reverse correlation between Firmicutes and Proteobacteria was observed, suggesting a possible antagonistic interaction between these two phyla. According to Pan and Yu (2014) alterations in one phyla or species may not only affect the host directly, but can also disrupt the entire microbial community. Notably, bacterial taxa belonging to the phyla Firmicutes are known to be involved in the degradation of complex carbohydrates (not absorbed by the host) and in the production of SCFAs (Thibodeau et al., 2015). Thus, the SCFAs production by Firmicutes might, at least partially, explain their dominance in the infected birds, which have a high SCFAs requirement as a source of energy for C. jejuni to colonize the chicken gut. Furthermore, Brown et al. (2012) reported that members of the phylum Firmicutes can inhibit the growth of opportunistic pathogens, such as E. coli, which has also been shown in the present study. Besides these major shifts, also low abundant phyla (e.g., Actinobacteria and Tenericutes) were affected by the Campylobacter infection, which could also disequilibrate the microbiome composition. Similarly, Johansen et al. (2006) found in a denaturing gradient gel electrophoresis (DGGE) based experiment that C. jejuni colonization affected the development and complexity of the microbial communities of the ceca over 17 days of age. Furthermore, Qu et al. (2008) noted that the community structure of the cecal microbiome from the C. jejuni challenged chicken has greater diversity and evenness with a higher abundance of Firmicutes at the expense of the Bacteroidetes and other taxa. Sofka et al. (2015) also reported that Campylobacter carriage, assessed in samples from slaughter houses, was associated with moderate modulations of the cecal microbiome as revealed by an increase in Streptococcus and Blautia relative abundance in birds of 56 days of age, originating from different farms and production types. Recently, Thibodeau et al. (2015) found also that C. jejuni colonization induced a moderate alteration of the chicken cecal microbiome beta-diversity at 35 days of age. This study's results strongly suggest that the Campylobacter associated alterations of the gut microbiota were a direct effect due to the interaction of C. jejuni with the microbiota or a consequence of the host responses or even a combination of both (Barman et al., 2008; Mon et al., 2015). The obtained results indicate that the influence of a Campylobacter infection on microbial communities was more pronounced at 14 dpi than at 7 dpi. This could be explained by an increased load of Camplyobacter at the later time point as demonstrated in recent studies using the same C. jejuni strain (Awad et al., 2014, 2015a,b, 2016). We also found significant differences in the abundance of certain bacterial species in the infected birds compared with the controls. C. jejuni caused a significant decrease in E. coli (best type strain hit) in the microbiota of infected birds in both jejunum and cecum. This is in agreement with our previous study which showed that Campylobacter colonization decreased E. coli loads in the jejunum and cecum at 7 dpi and at 14 dpi, but increased E. coli translocation to the liver and spleen of the infected birds as determined by conventional bacteriology (Awad et al., 2016). Thus, the current results pointed out that the relative abundance of E. coli could be an important determinant of susceptibility for a Campylobacter infection in particular and Gram-negative pathogens in general. In contrast to the Campylobacter -E. coli interaction, it was found that the relative abundance of Clostridium spp. was higher in the infected birds compared with the negative controls, indicating a link between C. jejuni and Clostridium. This confirms data from an earlier study in which a positive correlation between high levels of Clostridium perfringens (>6 log) and the colonization of C. jejuni were found by real-time quantitative PCR (Skånseng et al., 2006; Thibodeau et al., 2015). This might be due to the fact that C. jejuni acts as a hydrogen sink leading to improved growth conditions for some Clostridia through increased fermentation (Kaakoush et al., 2014). This link can also be explained by the fact that the Clostridium organic acid production could be used by C. jejuni as an energy source. Furthermore, it was found that a Campylobacter infection induces excess mucous production in the intestine (Molnár et al., 2015) which consequently may enhance Clostridium proliferation due to the fact that an increase in mucin secretion in the gut provides an opportunity for Clostridium spp. to proliferate (M'Sadeq et al., 2015). Overall, the higher abundance of Campylobacter and Clostridium spp. might result in a higher endotoxin production with subsequent increase in intestinal permeability that facilitates the colonization and enhances bacterial translocation from the intestine to the internal organs, which is well in agreement with our pervious results (Awad et al., 2015a, 2016). Finally, the strong shifts in the bacterial microbiome in the current study might help to explain why a Campylobacter infection is age dependent and chickens in the field become mainly colonized at an age of two to 4 weeks (Newell and Fearnley, 2003; Conlan et al., 2007). In agreement with this, Bereswill et al. (2011) demonstrated that a shift of intestinal microbiota in humans was linked with an increased susceptibility for C. jejuni. Finally, Haag et al. (2012) demonstrated that C. jejuni colonization in mice depends on the microbiota of the host and vice versa and Campylobacter colonization induces a shift of the intestinal microbiota. This was also observed in the present study as community structures were more dissimilar at the OTUs level in the infected birds compared with the controls. Moreover, in the infected birds, the population of beneficial microbes, such as E. coli and E. desmolans were comparatively lower than the potentially pathogenic bacteria, such as Clostridium spp., rendering the need for modulation of the gut microbiota to improve the gut health of the infected birds. Conclusion In the current study a substantial change in the composition of luminal and mucosa-associated gut microbiota in broiler chickens from day 1–28 was noticed. It could also be demonstrated that a C. jejuni infection in chickens was associated with significant changes in the composition of the intestinal ecosystem. Furthermore, these changes of the gut microbiota could lead to intestinal dysfunction, which has been evidenced in our previous studies. In this context, the results provide new insights into the microecological divergence of the intestinal microbiota with and without a Campylobacter infection and illustrate the C. jejuni–host crosstalk within the gut of broiler chickens. Understanding the relationship between disruption of the normal gut microbiota and Campylobacter infection may lead to improve in control strategies in order to minimize the consequences for the chicken host and the risk of bacterial spread to humans. Author contributions All authors listed, have made substantial, direct and intellectual contribution to the work, and approved it for publication. Conflict of interest statement The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. |
sec | Introduction A diverse microbiota is found throughout the gastrointestinal tract (GIT) of chickens, most predominant in the cecum (Mead, 1997; Videnska et al., 2014). The gut microbiota plays an essential role in nutrition, detoxification of certain compounds, growth performance and protection against pathogenic bacteria. The microbiota is crucial to strengthen the immune system, thereby affecting growth, health, and wellbeing of chicken. Generally, the gut microbiota modulates host responses to limit the colonization of pathogens (Rehman et al., 2007). There is little information about the diversity and function of the gut microbiota in chickens, its impact on the host and the impact of certain pathogens. Development of the gut microbiota in chickens occurs immediately after hatching and is influenced by both genetic and external factors like diet and environment (Apajalahti et al., 2004). It was reported that disturbances in the intestinal microbiota leads to a delay in growth, weakens the host resistance and increases the susceptibility to various infectious diseases (Lan et al., 2004). Gong et al. (2002) demonstrated that the cecal microbiota protects chickens against bacterial infections, while microbiota in the small intestine contributes significantly to its function, including digestion and nutrient absorption, which significantly determines the growth rate of the bird. Studies on gut microbiota have mostly been performed with chickens older than 1 week of age due to the various influences in day-old birds. However, the composition of gut microbiota at the first day of life in newly hatched chickens is a matter of interest within a longitudinal study. Therefore, the focus of the actual study was to determine the diversity and community structures of the microbiota within the small and large intestine from hatch until 4 weeks of age. Furthermore, differences among the mucosa-associated and luminal content microbiota were determined for the first time. Campylobacter (C.) jejuni is the most common cause of food-borne bacterial enteritis worldwide (EFSA, 2011). C. jejuni infection of chickens had previously not been considered to influence bird health and it was thought that C. jejuni is part of the normal microbiota of birds (EFSA, 2011). Understanding how Campylobacter species, especially C. jejuni, establishes successful colonization in chickens remains a foremost research priority as this gastrointestinal pathogen not only overcomes the host's defense system, but also competes with the microbial community for space and nutrients. It has been shown that Campylobacter requires numerous factors to successfully colonize the host, to translocate and to avoid clearance (Awad et al., 2014, 2015a,b, 2016; Humphrey et al., 2014). In addition, Awad et al. (2016) showed that Campylobacter had the ability to reduce butyrate, isobutyrate, valerate, and isovalerate which might be due to the utilization of short-chain fatty acids (SCFAs) as a carbon source (Masanta et al., 2013) or due to the reduction of butyric acid producing bacteria amongst the microbiota. In general, there is a complex interplay between microbiota composition and SCFAs concentration and it was found that the type and level of SCFAs in the gut can affect different members of the microbial community in various ways (Mon et al., 2015). It is still unknown how C. jejuni affects the ecology of the chicken gut, a feature of high importance considering a possible detrimental effect on the health of birds associated with C. jejuni colonization. Haag et al. (2012) demonstrated that C. jejuni colonization in mice depends on the microbiota of the host and vice versa and Campylobacter colonization induces a shift of the intestinal microbiota. Thus, it can be hypothesized that Campylobacter colonization is associated with an alteration in the intestinal microbiota of chickens as well. Therefore, the second aim of the actual study was to investigate the dynamics of an experimental Campylobacter jejuni NCTC 12744 infection in 14–28 days old chickens and the consequences on the alteration of the gut microbiome. |
title | Introduction |
p | A diverse microbiota is found throughout the gastrointestinal tract (GIT) of chickens, most predominant in the cecum (Mead, 1997; Videnska et al., 2014). The gut microbiota plays an essential role in nutrition, detoxification of certain compounds, growth performance and protection against pathogenic bacteria. The microbiota is crucial to strengthen the immune system, thereby affecting growth, health, and wellbeing of chicken. Generally, the gut microbiota modulates host responses to limit the colonization of pathogens (Rehman et al., 2007). There is little information about the diversity and function of the gut microbiota in chickens, its impact on the host and the impact of certain pathogens. |
p | Development of the gut microbiota in chickens occurs immediately after hatching and is influenced by both genetic and external factors like diet and environment (Apajalahti et al., 2004). It was reported that disturbances in the intestinal microbiota leads to a delay in growth, weakens the host resistance and increases the susceptibility to various infectious diseases (Lan et al., 2004). Gong et al. (2002) demonstrated that the cecal microbiota protects chickens against bacterial infections, while microbiota in the small intestine contributes significantly to its function, including digestion and nutrient absorption, which significantly determines the growth rate of the bird. Studies on gut microbiota have mostly been performed with chickens older than 1 week of age due to the various influences in day-old birds. However, the composition of gut microbiota at the first day of life in newly hatched chickens is a matter of interest within a longitudinal study. Therefore, the focus of the actual study was to determine the diversity and community structures of the microbiota within the small and large intestine from hatch until 4 weeks of age. Furthermore, differences among the mucosa-associated and luminal content microbiota were determined for the first time. |
p | Campylobacter (C.) jejuni is the most common cause of food-borne bacterial enteritis worldwide (EFSA, 2011). C. jejuni infection of chickens had previously not been considered to influence bird health and it was thought that C. jejuni is part of the normal microbiota of birds (EFSA, 2011). Understanding how Campylobacter species, especially C. jejuni, establishes successful colonization in chickens remains a foremost research priority as this gastrointestinal pathogen not only overcomes the host's defense system, but also competes with the microbial community for space and nutrients. |
p | It has been shown that Campylobacter requires numerous factors to successfully colonize the host, to translocate and to avoid clearance (Awad et al., 2014, 2015a,b, 2016; Humphrey et al., 2014). In addition, Awad et al. (2016) showed that Campylobacter had the ability to reduce butyrate, isobutyrate, valerate, and isovalerate which might be due to the utilization of short-chain fatty acids (SCFAs) as a carbon source (Masanta et al., 2013) or due to the reduction of butyric acid producing bacteria amongst the microbiota. In general, there is a complex interplay between microbiota composition and SCFAs concentration and it was found that the type and level of SCFAs in the gut can affect different members of the microbial community in various ways (Mon et al., 2015). |
p | It is still unknown how C. jejuni affects the ecology of the chicken gut, a feature of high importance considering a possible detrimental effect on the health of birds associated with C. jejuni colonization. Haag et al. (2012) demonstrated that C. jejuni colonization in mice depends on the microbiota of the host and vice versa and Campylobacter colonization induces a shift of the intestinal microbiota. Thus, it can be hypothesized that Campylobacter colonization is associated with an alteration in the intestinal microbiota of chickens as well. Therefore, the second aim of the actual study was to investigate the dynamics of an experimental Campylobacter jejuni NCTC 12744 infection in 14–28 days old chickens and the consequences on the alteration of the gut microbiome. |
sec | Materials and methods Ethics statement The animal experiment was approved by the institutional ethics committee of the University of Veterinary Medicine and the Ministry of Research and Science under the license number GZ 68.205/0011-11/3b/2013. All husbandry practices were performed with full consideration of animal welfare. Experimental design In this study, a total of 45 1-day-old broiler chickens (males and females) were obtained from a commercial hatchery (Ross-308, Geflügelhof Schulz, Graz, Austria). Five day-old birds were immediately sacrificed for determining the gut microbiota of the jejunal and cecal mucosa. At 7 and 14 days of age, five birds were randomly selected for measuring the development of gut microbiota from gut content and mucosa. The birds were kept as non-infected for the first 2 weeks and were housed on wood shavings with feed and water supplied ad libitum. The birds were fed a standard commercial diet for the whole experimental period in order to avoid an influence of the change of diet on the microbial composition. At the first and 14 days of age birds were confirmed as Campylobacter-free by taking cloacal swabs which were streaked onto modified charcoal-cefaprazone-deoxycholate agar (CM0739, OXOID, Hampshire, UK) and grown for 48 h under microaerophilic conditions at 42°C. At 14 days of age, 15 birds were infected with Campylobacter jejuni (C. jejuni) reference strain NCTC 12744 and kept separately from 15 non-infected control birds which were inoculated with PBS only. C. jejuni was routinely grown in Lennox L Base broth (LB broth) (Invitrogen, California, USA) at 42°C for 48 h in a shaking incubator. Campylobacter colony-forming unit (CFU) was determined from each suspension by serial dilutions in duplicate using LB agar. Campylobacter suspensions were stored at −80°C by adding 2 mL of 40% glycerol/10 mL LB broth. For infection, Campylobacter suspensions were centrifuged for 5 min at 10,000 × rpm. The pellet was washed 3 times with phosphate-buffered saline (PBS) each time centrifuged at the same conditions as mentioned above. Finally, the pellets were resuspended in PBS and the necessary concentration was adjusted for birds' infection. The infection was performed orally via feeding tube (gavage) with a dose of 1 × 108 CFU/bird at 14 days of age as described previously (Awad et al., 2015a). At 7 days post infection 5 birds from each group were anesthetized by injection of a single dose of thiopental (20 mg/kg) into the wing vein and slaughtered by bleeding of the jugular vein. The final 10 birds/group were killed at 14 days post infection. At each time point the gastrointestinal content from the jejunum and ceca, as well as jejunal and cecal mucosa from 5 birds/group were taken to determine the gut microbiota. Intestinal segments were disclosed at the mesentery with sterile instruments and the digesta was removed. The luminal site of the intestinal segments was washed with sterile ice-cold PBS until the mucosa was completely cleaned from the digesta. The mucosa was rinsed several times with sterile ice cold PBS, after which the mucosa was collected aseptically by scraping off the mucosa using scalpel blades. All samples were stored at −80°C until further processing. DNA extraction, PCR amplification of the 16S rRNA gene, and illumina MISeq sequencing DNA from luminal content and gut mucosa samples was extracted using the PowerSoil® DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA, USA) as described previously (Mann et al., 2014; Yasuda et al., 2015). The same protocol of DNA extraction was applied to luminal content and gut mucosa. From each of the 130 samples a total of 250 mg of gut content or mucosa was used for DNA isolation according to manufacturer's instructions. DNA concentration was determined by a Qubit fluorometer (Invitrogen, Carlsbad, CA, USA). The V345 hypervariable region of the 16S rRNA genes was amplified with the primers F341 (5′-GTGYCAGCMGCCGCGGTAA-3′) (Zakrzewski et al., 2012) and R909 (5′-CCGYCAATTYMTTTRAGTTT-3′) (Tamaki et al., 2011). An amplicon size of approximately 568 bp was produced. 16S rRNA gene PCRs, library preparation and sequencing were performed by Microsynth (Microsynth AG, Balgach Switzerland). Libraries were constructed by ligating sequencing adapters and indices onto purified PCR products using the Nextera XT Sample Preparation Kit (Illumina) and equimolar amounts of each of the libraries were pooled and sequenced on an Illumina MiSeq Sequencing Platform. Sequence data were analyzed with the software package QIIME (Caporaso et al., 2010). Low quality sequences (q < 20) were filtered, chimeric sequences were excluded by using the USEARCH 6.1 database (Edgar, 2010) and sequences were clustered into operational taxonomic units (OTUs; 97% similarity) with the QIIME script “pick_open_reference_otus.py.” OTUs with less than 10 sequences were removed, resulting in 8285 OTUs, which were used for all downstream analysis. The representative sequences of the 50 most abundant OTUs over all sampling time points were classified against type strains using the Greengenes database (http://greengenes.lbl.gov) (DeSantis et al., 2006). Microbial diversity analysis Both alpha and beta diversity indices were used to estimate the microbiome diversity within—and between microbial communities. Calculations were done with the “summary.single” command in the software package mothur (http://www.mothur.org/; Kozich et al., 2013). Alpha diversity indices analysis included Chao1 index (richness estimate), abundance-based coverage estimator (ACE, richness estimate), Shannon's diversity, and Simpson's diversity index. For the Bray-Curtis similarity, the dataset was rarefied to the minimum number of sequences per sample. Rarefaction curve was constructed based on the observed number of OTUs and nearly reached asymptotes for all samples (data not shown). Principal component analysis was done with JMP® (Version 10.0.0, SAS Institute Inc., Cary, NC). Shared OTUs among gut sites at different age were plotted as Venn diagrams using the R environment (package “VennDiagram,” version 1.6.17.) (Chen, 2016). Heatmaps were created using JColorGrid (Joachimiak et al., 2006). Statistical analysis Statistically significant differences in relative abundance with regard to sampling sites and time were calculated using “metastats” in mothur, which is based on the homonymous bioinformatics program (White et al., 2009; Paulson et al., 2011). “Metastats” uses repeated t statistics and Fisher's tests on random permutations to handle sparsely-sampled features (White et al., 2009). Results were reported as a mean and standard deviation (SD). The significance level was set to P < 0.05. The P-values were adjusted with the Benjamini and Hochberg false discovery rate correction (FDR, q-value), and a q < 0.25 was considered significant (Lim et al., 2016). Furthermore, significant differences between the diversity estimators of the two groups were performed using the non-parametric Kruskal-Wallis-test followed by Mann-Whitney-test. PASW statistics 20, SPSS software (Chicago, Il., USA) was used for statistical analyses of diversity estimators. Accession numbers Sequencing data are available in the European Nucleotide Archive (ENA) database under the accession number PRJEB14860. |
title | Materials and methods |
sec | Ethics statement The animal experiment was approved by the institutional ethics committee of the University of Veterinary Medicine and the Ministry of Research and Science under the license number GZ 68.205/0011-11/3b/2013. All husbandry practices were performed with full consideration of animal welfare. |
title | Ethics statement |
p | The animal experiment was approved by the institutional ethics committee of the University of Veterinary Medicine and the Ministry of Research and Science under the license number GZ 68.205/0011-11/3b/2013. All husbandry practices were performed with full consideration of animal welfare. |
sec | Experimental design In this study, a total of 45 1-day-old broiler chickens (males and females) were obtained from a commercial hatchery (Ross-308, Geflügelhof Schulz, Graz, Austria). Five day-old birds were immediately sacrificed for determining the gut microbiota of the jejunal and cecal mucosa. At 7 and 14 days of age, five birds were randomly selected for measuring the development of gut microbiota from gut content and mucosa. The birds were kept as non-infected for the first 2 weeks and were housed on wood shavings with feed and water supplied ad libitum. The birds were fed a standard commercial diet for the whole experimental period in order to avoid an influence of the change of diet on the microbial composition. At the first and 14 days of age birds were confirmed as Campylobacter-free by taking cloacal swabs which were streaked onto modified charcoal-cefaprazone-deoxycholate agar (CM0739, OXOID, Hampshire, UK) and grown for 48 h under microaerophilic conditions at 42°C. At 14 days of age, 15 birds were infected with Campylobacter jejuni (C. jejuni) reference strain NCTC 12744 and kept separately from 15 non-infected control birds which were inoculated with PBS only. C. jejuni was routinely grown in Lennox L Base broth (LB broth) (Invitrogen, California, USA) at 42°C for 48 h in a shaking incubator. Campylobacter colony-forming unit (CFU) was determined from each suspension by serial dilutions in duplicate using LB agar. Campylobacter suspensions were stored at −80°C by adding 2 mL of 40% glycerol/10 mL LB broth. For infection, Campylobacter suspensions were centrifuged for 5 min at 10,000 × rpm. The pellet was washed 3 times with phosphate-buffered saline (PBS) each time centrifuged at the same conditions as mentioned above. Finally, the pellets were resuspended in PBS and the necessary concentration was adjusted for birds' infection. The infection was performed orally via feeding tube (gavage) with a dose of 1 × 108 CFU/bird at 14 days of age as described previously (Awad et al., 2015a). At 7 days post infection 5 birds from each group were anesthetized by injection of a single dose of thiopental (20 mg/kg) into the wing vein and slaughtered by bleeding of the jugular vein. The final 10 birds/group were killed at 14 days post infection. At each time point the gastrointestinal content from the jejunum and ceca, as well as jejunal and cecal mucosa from 5 birds/group were taken to determine the gut microbiota. Intestinal segments were disclosed at the mesentery with sterile instruments and the digesta was removed. The luminal site of the intestinal segments was washed with sterile ice-cold PBS until the mucosa was completely cleaned from the digesta. The mucosa was rinsed several times with sterile ice cold PBS, after which the mucosa was collected aseptically by scraping off the mucosa using scalpel blades. All samples were stored at −80°C until further processing. |
title | Experimental design |
p | In this study, a total of 45 1-day-old broiler chickens (males and females) were obtained from a commercial hatchery (Ross-308, Geflügelhof Schulz, Graz, Austria). Five day-old birds were immediately sacrificed for determining the gut microbiota of the jejunal and cecal mucosa. At 7 and 14 days of age, five birds were randomly selected for measuring the development of gut microbiota from gut content and mucosa. The birds were kept as non-infected for the first 2 weeks and were housed on wood shavings with feed and water supplied ad libitum. The birds were fed a standard commercial diet for the whole experimental period in order to avoid an influence of the change of diet on the microbial composition. |
p | At the first and 14 days of age birds were confirmed as Campylobacter-free by taking cloacal swabs which were streaked onto modified charcoal-cefaprazone-deoxycholate agar (CM0739, OXOID, Hampshire, UK) and grown for 48 h under microaerophilic conditions at 42°C. At 14 days of age, 15 birds were infected with Campylobacter jejuni (C. jejuni) reference strain NCTC 12744 and kept separately from 15 non-infected control birds which were inoculated with PBS only. C. jejuni was routinely grown in Lennox L Base broth (LB broth) (Invitrogen, California, USA) at 42°C for 48 h in a shaking incubator. Campylobacter colony-forming unit (CFU) was determined from each suspension by serial dilutions in duplicate using LB agar. Campylobacter suspensions were stored at −80°C by adding 2 mL of 40% glycerol/10 mL LB broth. For infection, Campylobacter suspensions were centrifuged for 5 min at 10,000 × rpm. The pellet was washed 3 times with phosphate-buffered saline (PBS) each time centrifuged at the same conditions as mentioned above. Finally, the pellets were resuspended in PBS and the necessary concentration was adjusted for birds' infection. |
p | The infection was performed orally via feeding tube (gavage) with a dose of 1 × 108 CFU/bird at 14 days of age as described previously (Awad et al., 2015a). At 7 days post infection 5 birds from each group were anesthetized by injection of a single dose of thiopental (20 mg/kg) into the wing vein and slaughtered by bleeding of the jugular vein. The final 10 birds/group were killed at 14 days post infection. At each time point the gastrointestinal content from the jejunum and ceca, as well as jejunal and cecal mucosa from 5 birds/group were taken to determine the gut microbiota. Intestinal segments were disclosed at the mesentery with sterile instruments and the digesta was removed. The luminal site of the intestinal segments was washed with sterile ice-cold PBS until the mucosa was completely cleaned from the digesta. The mucosa was rinsed several times with sterile ice cold PBS, after which the mucosa was collected aseptically by scraping off the mucosa using scalpel blades. All samples were stored at −80°C until further processing. |
sec | DNA extraction, PCR amplification of the 16S rRNA gene, and illumina MISeq sequencing DNA from luminal content and gut mucosa samples was extracted using the PowerSoil® DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA, USA) as described previously (Mann et al., 2014; Yasuda et al., 2015). The same protocol of DNA extraction was applied to luminal content and gut mucosa. From each of the 130 samples a total of 250 mg of gut content or mucosa was used for DNA isolation according to manufacturer's instructions. DNA concentration was determined by a Qubit fluorometer (Invitrogen, Carlsbad, CA, USA). The V345 hypervariable region of the 16S rRNA genes was amplified with the primers F341 (5′-GTGYCAGCMGCCGCGGTAA-3′) (Zakrzewski et al., 2012) and R909 (5′-CCGYCAATTYMTTTRAGTTT-3′) (Tamaki et al., 2011). An amplicon size of approximately 568 bp was produced. 16S rRNA gene PCRs, library preparation and sequencing were performed by Microsynth (Microsynth AG, Balgach Switzerland). Libraries were constructed by ligating sequencing adapters and indices onto purified PCR products using the Nextera XT Sample Preparation Kit (Illumina) and equimolar amounts of each of the libraries were pooled and sequenced on an Illumina MiSeq Sequencing Platform. Sequence data were analyzed with the software package QIIME (Caporaso et al., 2010). Low quality sequences (q < 20) were filtered, chimeric sequences were excluded by using the USEARCH 6.1 database (Edgar, 2010) and sequences were clustered into operational taxonomic units (OTUs; 97% similarity) with the QIIME script “pick_open_reference_otus.py.” OTUs with less than 10 sequences were removed, resulting in 8285 OTUs, which were used for all downstream analysis. The representative sequences of the 50 most abundant OTUs over all sampling time points were classified against type strains using the Greengenes database (http://greengenes.lbl.gov) (DeSantis et al., 2006). |
title | DNA extraction, PCR amplification of the 16S rRNA gene, and illumina MISeq sequencing |
p | DNA from luminal content and gut mucosa samples was extracted using the PowerSoil® DNA Isolation Kit (MoBio Laboratories, Carlsbad, CA, USA) as described previously (Mann et al., 2014; Yasuda et al., 2015). The same protocol of DNA extraction was applied to luminal content and gut mucosa. From each of the 130 samples a total of 250 mg of gut content or mucosa was used for DNA isolation according to manufacturer's instructions. DNA concentration was determined by a Qubit fluorometer (Invitrogen, Carlsbad, CA, USA). The V345 hypervariable region of the 16S rRNA genes was amplified with the primers F341 (5′-GTGYCAGCMGCCGCGGTAA-3′) (Zakrzewski et al., 2012) and R909 (5′-CCGYCAATTYMTTTRAGTTT-3′) (Tamaki et al., 2011). An amplicon size of approximately 568 bp was produced. |
p | 16S rRNA gene PCRs, library preparation and sequencing were performed by Microsynth (Microsynth AG, Balgach Switzerland). Libraries were constructed by ligating sequencing adapters and indices onto purified PCR products using the Nextera XT Sample Preparation Kit (Illumina) and equimolar amounts of each of the libraries were pooled and sequenced on an Illumina MiSeq Sequencing Platform. Sequence data were analyzed with the software package QIIME (Caporaso et al., 2010). Low quality sequences (q < 20) were filtered, chimeric sequences were excluded by using the USEARCH 6.1 database (Edgar, 2010) and sequences were clustered into operational taxonomic units (OTUs; 97% similarity) with the QIIME script “pick_open_reference_otus.py.” OTUs with less than 10 sequences were removed, resulting in 8285 OTUs, which were used for all downstream analysis. The representative sequences of the 50 most abundant OTUs over all sampling time points were classified against type strains using the Greengenes database (http://greengenes.lbl.gov) (DeSantis et al., 2006). |
sec | Microbial diversity analysis Both alpha and beta diversity indices were used to estimate the microbiome diversity within—and between microbial communities. Calculations were done with the “summary.single” command in the software package mothur (http://www.mothur.org/; Kozich et al., 2013). Alpha diversity indices analysis included Chao1 index (richness estimate), abundance-based coverage estimator (ACE, richness estimate), Shannon's diversity, and Simpson's diversity index. For the Bray-Curtis similarity, the dataset was rarefied to the minimum number of sequences per sample. Rarefaction curve was constructed based on the observed number of OTUs and nearly reached asymptotes for all samples (data not shown). Principal component analysis was done with JMP® (Version 10.0.0, SAS Institute Inc., Cary, NC). Shared OTUs among gut sites at different age were plotted as Venn diagrams using the R environment (package “VennDiagram,” version 1.6.17.) (Chen, 2016). Heatmaps were created using JColorGrid (Joachimiak et al., 2006). |
title | Microbial diversity analysis |
p | Both alpha and beta diversity indices were used to estimate the microbiome diversity within—and between microbial communities. Calculations were done with the “summary.single” command in the software package mothur (http://www.mothur.org/; Kozich et al., 2013). Alpha diversity indices analysis included Chao1 index (richness estimate), abundance-based coverage estimator (ACE, richness estimate), Shannon's diversity, and Simpson's diversity index. |
p | For the Bray-Curtis similarity, the dataset was rarefied to the minimum number of sequences per sample. Rarefaction curve was constructed based on the observed number of OTUs and nearly reached asymptotes for all samples (data not shown). |
p | Principal component analysis was done with JMP® (Version 10.0.0, SAS Institute Inc., Cary, NC). Shared OTUs among gut sites at different age were plotted as Venn diagrams using the R environment (package “VennDiagram,” version 1.6.17.) (Chen, 2016). Heatmaps were created using JColorGrid (Joachimiak et al., 2006). |
sec | Statistical analysis Statistically significant differences in relative abundance with regard to sampling sites and time were calculated using “metastats” in mothur, which is based on the homonymous bioinformatics program (White et al., 2009; Paulson et al., 2011). “Metastats” uses repeated t statistics and Fisher's tests on random permutations to handle sparsely-sampled features (White et al., 2009). Results were reported as a mean and standard deviation (SD). The significance level was set to P < 0.05. The P-values were adjusted with the Benjamini and Hochberg false discovery rate correction (FDR, q-value), and a q < 0.25 was considered significant (Lim et al., 2016). Furthermore, significant differences between the diversity estimators of the two groups were performed using the non-parametric Kruskal-Wallis-test followed by Mann-Whitney-test. PASW statistics 20, SPSS software (Chicago, Il., USA) was used for statistical analyses of diversity estimators. |
title | Statistical analysis |
p | Statistically significant differences in relative abundance with regard to sampling sites and time were calculated using “metastats” in mothur, which is based on the homonymous bioinformatics program (White et al., 2009; Paulson et al., 2011). “Metastats” uses repeated t statistics and Fisher's tests on random permutations to handle sparsely-sampled features (White et al., 2009). Results were reported as a mean and standard deviation (SD). The significance level was set to P < 0.05. The P-values were adjusted with the Benjamini and Hochberg false discovery rate correction (FDR, q-value), and a q < 0.25 was considered significant (Lim et al., 2016). Furthermore, significant differences between the diversity estimators of the two groups were performed using the non-parametric Kruskal-Wallis-test followed by Mann-Whitney-test. PASW statistics 20, SPSS software (Chicago, Il., USA) was used for statistical analyses of diversity estimators. |
sec | Accession numbers Sequencing data are available in the European Nucleotide Archive (ENA) database under the accession number PRJEB14860. |
title | Accession numbers |
p | Sequencing data are available in the European Nucleotide Archive (ENA) database under the accession number PRJEB14860. |
sec | Results Sequence analysis, phylum and OTU classification Sequencing of 130 samples yielded 51,825,306 quality-controlled sequences, clustering into 8285 operational taxonomic units (OTUs; 0.03 distance level). Throughout all gut sites 24 phyla were identified with Firmicutes, Proteobacteria, and Tenericutes being the most abundant ones. In Figure S1A, Tables S1A–D, relative abundances of all phyla are delineated with respect to age and groups. The results showed that in the jejunum and cecum, Firmicutes and Proteobacteria were the dominating luminal and mucosal-associated phyla in all birds investigated (Tables S2, S3). At the first day of life Proteobacteria were significantly higher in the jejunal (P = 0.0000, q = 0.0000) and cecal (P = 0.016; q = 0.059) mucosa of the birds and decreased thereafter, as no significant differences were found between samples from day 14 to day 28 of age (P = 0.140; q = 0.438 and P = 0.519; q = 0.955). On the contrary, Firmicutes were significantly lower at day 1 and increased thereafter (P = 0.001; q = 0.016 and P = 0.006; q = 0.055 in the jejunal and cecal mucosa, respectively). For infected birds, relative abundances of bacterial phyla at the two sampling time points carried out post infection are represented in Figure S1B, Tables S4A–D. Figure 1 shows that the phylum Proteobacteria decreased while Firmicutes increased at either 21 (7 dpi) or 28 days of age (14 dpi). There was a significant decrease in Actinobacteria and Proteobacteria in the jejunal mucosa at 14 dpi (P = 0.006; q = 0.100 and P = 0.005; q = 0.100), while Firmicutes and Bacteroidetes were more abundant in the infected birds compared to the controls (P = 0.005; q = 0.100 and P = 0.023; q = 0.217, Table S4A). However, in the cecal content and cecal mucosa, Bacteroidetes (P = 0.001; q = 0.019) increased at 7 dpi, but decreased (P = 0.002; q = 0.026 and P = 0.005; q = 0.048) at 14 dpi in the infected birds compared with the controls, indicating that the Campylobacter infection modulates the jejunal and cecal phylum abundances in different ways. Figure 1 Relative abundances (%) of the most abundant phyla in the infected birds compared with the controls at the two sampling points post infection of (A) jejunum and (B) cecum. Data are presented as the mean values and standard deviation (SD). JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i). In Table 1, the 50 most abundant OTUs from all birds are listed including the internal OTU number, relative abundance together with the reference strain and similarity (compared with strains of the Greengenes database). Relative OTUs abundances at different ages in all birds are shown in Tables S5A–D, S6A–D. The OTUs and species abundances sorted by age at the four gut sites of the birds are shown in the heatmaps of Figure S2. In total, the 50 most abundant OTUs accounted for 73.9% of all sequences and of those 42 OTUs differed significantly in their relative abundances over all gut sites independent of the age (Tables 2, 3). At the first day of age, a notable high relative abundance of OTU 1, 25, 27, and 35 (best type strain hits: Escherichia coli, Enterococcus faecalis, Clostridium paraputrificum, and Clostridium sartagoforme) were found in both jejunal and cecal mucosa (Tables S5A,C), whereas OTU 38 (best type strain hit: Acinetobacter johnsonii) was only abundant in the jejunal mucosa and OTU 42 (best type strain hit: C. paraputrificum) was only abundant in the cecal mucosa. All these abundant OTUs decreased by age. In the jejunal mucosa, OTU 1 was the most abundant (57.9%), followed by the other four OTUs which ranged between 2.6 and 7.9%. Similarly, in the mucosa of the cecum, OTU 1 was highly abundant (65.9%), followed by OTUs 27, 25, 35, and 42 which ranged between 7.8 and 3.3%. Table 1 The 50 most abundant OTUs retrieved from different gut sites from all birds independent of the infection status. OTUs No. of sequences Relative abundance (%) Best type strain hita Similarity (%) OTU 1 642068 10.64 Escherichia coli (GU968184.1) 100 OTU 2 341923 5.66 Lactobacillus johnsonii (HM772969.1) 100 OTU 3 339288 5.62 Lactobacillus salivarius (NZ_AEBA01000145.1) 100 OTU 4 310060 5.14 Clostridium spp. (FJ808599.1) 87 OTU 5 273783 4.54 Enterococcus durans (FJ917726.1) 100 OTU 6 209121 3.46 Anaerotruncus colihominis (NR_027558.1) 100 OTU 7 208070 3.45 Eubacterium desmolans (L34618.1) 98 OTU 8 161864 2.68 Clostridium cellulolyticum (X71847.1) 87 OTU 9 157466 2.61 Spiroplasma lampyridicola (AY189134.1) 82 OTU 10 151864 2.52 Clostridium leptum (AJ305238.1) 97 OTU 11 130587 2.16 Eubacterium desmolans (L34618.1) 99 OTU 12 127446 2.11 Eubacterium desmolans (L34618.1) 98 OTU 13 120732 2.00 Clostridium papyrosolvens (NR_026102.1) 87 OTU 14 113436 1.88 Eubacterium coprostanoligenes (HM037995.1) 92 OTU 15 98491 1.63 Clostridium straminisolvens (NR_024829.1); Clostridium thermocellum (AB558166.1) 87 OTU 16 87863 1.46 Clostridium cellulolyticum (NC_011898.1) 87 OTU 17 70842 1.17 Bacillus subtilis (FJ608705.1) 94 OTU 18 67038 1.11 Lactobacillus reuteri (EU547311.1) 99 OTU 19 66212 1.10 Ruminococcus bromii (NR_025930.1) 94 OTU 20 65592 1.09 Eubacterium desmolans (L34618.1) 95 OTU 21 53133 0.88 Clostridium cellulolyticum (NC_011898.1); Clostridium papyrosolvens (NR_026102.1) 87 OTU 22 49736 0.82 Clostridium thermocellum (AB558166.1) 85 OTU 23 47570 0.79 Clostridium thermosuccinogenes (Y18180.1); Clostridium thermocellum (AB558166.1) 86 OTU 24 40373 0.67 Clostridium leptum (AJ305238.1) 95 OTU 25 36925 0.61 Enterococcus faecalis (FJ607291.1) 100 OTU 26 35311 0.58 Proteus mirabilis (GU477712.1) 100 OTU 27 31154 0.52 Clostridium paraputrificum (AY442815.1) 100 OTU 28 29186 0.48 Variovorax paradoxus (HQ005421.1) 100 OTU 29 28876 0.48 Campylobacter subsp. jejuni (NC_008787.1) 100 OTU 30 27988 0.46 Clostridium leptum (AJ305238.1) 93 OTU 31 23587 0.39 Anaerotruncus colihominis (NR_027558.1) 93 OTU 32 23559 0.39 Lactobacillus crispatus (FN692037.1) 100 OTU 33 22863 0.38 Phyllobacterium myrsinacearum (AY785330.1) 100 OTU 34 21547 0.36 Catabacter hongkongensis (AY574991.1); Clostridium thermosuccinogenes (Y18180.1) 86 OTU 35 20378 0.34 Clostridium sartagoforme (FJ384380.1) 100 OTU 36 18849 0.31 Acetivibrio cellulolyticus (L35515.1) 95 OTU 37 18055 0.30 Clostridium papyrosolvens (NR_026102.1) 86 OTU 38 17890 0.30 Acinetobacter johnsonii (EU977694.1) 100 OTU 39 15658 0.26 Clostridium papyrosolvens (NR_026102.1) 87 OTU 40 15361 0.25 Lactobacillus johnsonii (EU381128.1) 96 OTU 41 15143 0.25 Clostridium thermosuccinogenes (Y18180.1) 87 OTU 42 14985 0.25 Clostridium paraputrificum (AY442815.1) 100 OTU 43 14682 0.24 Marinobacter sp. (FJ889664.1) 99 OTU 44 14652 0.24 Clostridium papyrosolvens (NR_026102.1) 87 OTU 45 14304 0.24 Shigella flexneri (CP000266.1) 99 OTU 46 13619 0.23 Clostridium cellulolyticum (NC_011898.1) 86 OTU 47 13307 0.22 Clostridium papyrosolvens (NR_026102.1) 86 OTU 48 13152 0.22 Clostridium papyrosolvens (NR_026102.1) 87 OTU 49 12978 0.21 Clostridium papyrosolvens (NR_026102.1) 87 OTU 50 12418 0.21 Lactobacillus salivarius (NZ_AEBA01000145.1) 98 a Greengenes best type strain hit accession numbers are listed in parenthesis. Table 2 Relative abundances (%) of the most abundant OTUs in different gut sites of control birds (day 1–28). OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa OTU 49 0 0.02 0.05 0.11 0.01 0.02 0.01 0.02 0.056 0.164 0.655 0.858 0.366 0.623 0.133 0.326 OTU 25 1.89 4.01 0.06 0.07 1.05 2.95 0.01 0.02 0.001 0.011 0.015 0.067 0.365 0.623 0.001 0.011 OTU 5 12.41 25.84 13.09 21.85 0.28 0.56 0.07 0.09 0.920 0.990 0.039 0.134 0.002 0.017 0.001 0.011 OTU 30 0.45 1.45 0.40 0.72 0.74 1.11 1.25 2.09 0.913 0.990 0.385 0.643 0.808 0.946 0.059 0.170 OTU 9 0.90 2.72 1.03 3.05 3.56 9.78 5.82 15.04 0.938 0.990 0.514 0.765 0.196 0.401 0.091 0.244 OTU 13 1.34 5.22 0.75 1.84 1.36 4.51 1.41 4.43 0.714 0.890 0.831 0.946 0.940 0.990 0.549 0.770 OTU 15 0.07 0.20 0.13 0.32 1.17 1.98 4.21 9.38 0.792 0.942 0.095 0.250 0.005 0.030 0.001 0.011 OTU 18 2.36 8.46 2.34 6.03 0.08 0.23 0.03 0.09 0.961 0.994 0.409 0.665 0.081 0.220 0.013 0.059 OTU 21 0.65 2.01 0.32 0.87 0.53 1.11 1.08 3.21 0.588 0.787 0.599 0.796 0.812 0.946 0.294 0.526 OTU 33 0.96 1.38 2.57 5.92 0 0 0 0 0.341 0.603 0.001 0.011 OTU 12 0.95 2.20 1.25 4.71 2.42 5.21 5.41 11.82 0.776 0.929 0.285 0.519 0.491 0.739 0.131 0.326 OTU 28 3.21 7.19 2.99 7.77 0 0 0 0 0.941 0.990 0.006 0.034 0.001 0.011 0.001 0.011 OTU 37 0.12 0.56 0 0.01 0.39 1.93 0.07 0.28 0.140 0.326 0.939 0.990 0.947 0.991 0.177 0.379 OTU 40 0.05 0.11 1.08 1.53 0 0 0.10 0.44 0.001 0.011 0.464 0.722 0.001 0.011 0.008 0.043 OTU 3 10.36 20.66 18.43 23.28 0.39 0.63 1.52 5.30 0.252 0.475 0.517 0.765 0.001 0.011 0.002 0.017 OTU 26 0.03 0.07 0.03 0.06 1.34 2.35 1.75 3.25 0.483 0.737 0.691 0.875 0.001 0.011 0.003 0.020 OTU 19 0.80 1.99 0.22 0.57 1.09 2.22 1.01 2.17 0.189 0.395 0.979 0.997 0.961 0.994 0.134 0.326 OTU 44 0.04 0.15 0.02 0.04 0.06 0.12 0.07 0.14 0.748 0.908 0.660 0.858 0.452 0.715 0.052 0.155 OTU 39 0.02 0.07 0.01 0.02 0.07 0.20 0.08 0.19 0.769 0.927 0.726 0.893 0.253 0.475 0.046 0.147 OTU 29 0 0 0 0 0 0 0 0 0.002 0.017 OTU 2 10.86 14.76 24.38 24.19 0.13 0.26 0.31 1.13 0.046 0.147 0.817 0.946 0.001 0.011 0.001 0.011 OTU 38 1.51 5.31 0.17 0.67 0 0 0 0 0.145 0.326 0.002 0.017 OTU 42 0.51 1.20 0.01 0.03 0.67 1.71 0.01 0.03 0.012 0.057 0.041 0.136 0.717 0.890 0.669 0.864 OTU 17 0.46 1.30 0.02 0.05 2.79 7.57 0.05 0.15 0.041 0.136 0.063 0.176 0.243 0.466 0.571 0.770 OTU 1 14.87 24.08 5.33 7.93 22.17 26.59 13.03 17.69 0.069 0.190 0.231 0.452 0.295 0.526 0.062 0.176 OTU 11 0.69 1.32 0.51 0.97 2.63 7.62 3.10 5.11 0.362 0.623 0.692 0.875 0.458 0.719 0.003 0.020 OTU 4 0.51 2.00 0.17 0.56 1.34 4.60 2.14 7.58 0.571 0.770 0.611 0.806 0.525 0.770 0.147 0.326 OTU 48 0 0 0 0 0 0 0 0 0.036 0.131 OTU 14 0.24 0.69 0.22 0.43 3.77 8.30 4.66 10.97 0.542 0.770 0.747 0.908 0.023 0.091 0.004 0.025 OTU 46 0 0.02 0.01 0.02 0.26 0.65 0.25 0.50 0.348 0.609 0.991 1.000 0.028 0.106 0.039 0.134 OTU 31 0.23 0.55 0.05 0.12 0.87 1.67 0.33 0.51 0.137 0.326 0.170 0.368 0.166 0.364 0.016 0.068 OTU 45 0.05 0.09 0.01 0.01 0.35 0.56 1.02 1.62 0.023 0.091 0.096 0.250 0.016 0.068 0.004 0.025 OTU 10 0.37 1.03 0.20 0.46 4.39 11.22 4.97 10.40 0.477 0.736 0.824 0.946 0.013 0.059 0.003 0.020 OTU 32 0.12 0.43 0.23 0.79 0 0 0 0 0.540 0.770 0.868 0.975 0.012 0.057 0.006 0.034 OTU 8 0.28 1.29 0.03 0.10 1.43 5.01 2.34 7.10 0.537 0.770 0.551 0.770 0.370 0.624 0.138 0.326 OTU 6 1.17 3.54 0.13 0.28 9.20 15.81 1.39 1.56 0.238 0.461 0.007 0.039 0.021 0.087 0.001 0.011 OTU 36 0.03 0.11 0.11 0.22 0.68 1.66 0.25 0.49 0.144 0.326 0.263 0.488 0.003 0.020 0.220 0.445 OTU 35 0.57 1.28 0.02 0.04 0.90 2.13 0.02 0.08 0.012 0.057 0.034 0.126 0.542 0.770 0.867 0.975 OTU 7 1.07 2.73 1.41 2.66 3.52 7.28 6.47 12.19 0.832 0.946 0.282 0.518 0.125 0.320 0.037 0.132 OTU 16 0.73 3.50 0.27 1.01 1.41 3.77 1.96 4.92 0.905 0.990 0.562 0.770 0.400 0.656 0.146 0.326 OTU 27 0.98 2.31 0.02 0.07 1.56 4.02 0.01 0.05 0.012 0.057 0.048 0.151 0.563 0.770 0.719 0.890 OTU 20 1.68 4.52 0.05 0.18 0.86 4.28 0.91 4.07 0.049 0.151 0.981 0.997 0.448 0.715 0.997 1.000 OTU 50 0.09 0.15 0.84 0.95 0 0.01 0.06 0.23 0.001 0.011 0.486 0.737 0.001 0.011 0.002 0.017 OTU 22 0 0 0 0.02 0 0 0 0.01 0.231 0.452 0.882 0.985 OTU 47 0.12 0.53 0 0.02 0.32 1.55 0.06 0.22 0.191 0.395 0.917 0.990 0.933 0.990 0.180 0.381 OTU 41 0 0.01 0 0 0 0 0 0 0.228 0.452 1.000 1.000 OTU 23 0.12 0.50 0.01 0.02 0.07 0.20 0.09 0.23 0.136 0.326 0.682 0.874 0.819 0.946 0.024 0.093 OTU 43 0.01 0.03 0 0 0 0 0 0 OTU 34 0.03 0.14 0 0 0.06 0.16 0.14 0.38 0.903 0.990 0.417 0.672 0.390 0.645 0.051 0.155 OTU 24 0.11 0.52 0.18 0.39 1.18 1.89 1.10 1.90 0.567 0.770 0.973 0.997 0.001 0.011 0.003 0.020 a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. Table 3 Relative abundances (%) of the most abundant OTUs in different gut sites of infected birds (days 21 and 28). OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa OTU 49 0.18 0.28 0.43 0.98 0.61 1.44 0.52 0.91 0.689 0.880 0.936 0.989 0.550 0.791 0.516 0.776 OTU 25 0.02 0.04 0.08 0.09 0.00 0.00 0 0 0.077 0.178 0.063 0.168 OTU 5 1.65 2.21 8.89 6.18 0.01 0.01 0 0 0.009 0.043 0.761 0.927 0.001 0.007 0.001 0.007 OTU 30 0.31 0.94 0.06 0.08 0.30 0.38 0.16 0.12 0.957 0.989 0.355 0.596 1.000 1.000 0.013 0.056 OTU 9 0.17 0.39 0.14 0.14 1.47 4.29 2.06 5.88 0.903 0.987 0.575 0.791 0.530 0.785 0.217 0.408 OTU 13 0.64 1.06 0.72 1.35 2.87 3.77 2.65 2.58 0.955 0.989 0.950 0.989 0.056 0.159 0.020 0.071 OTU 15 0.08 0.13 0.01 0.02 1.24 0.89 2.13 1.23 0.049 0.146 0.040 0.126 0.001 0.007 0.001 0.007 OTU 18 4.67 9.39 6.34 11.77 0.19 0.44 0.14 0.36 0.572 0.791 0.857 0.986 0.102 0.218 0.011 0.051 OTU 21 0.28 0.58 0.16 0.19 1.63 2.60 1.93 2.41 0.565 0.791 0.611 0.611 0.085 0.191 0.009 0.043 OTU 33 1.11 1.14 0.13 0.13 0.00 0.00 0.00 0.00 0.008 0.041 1.000 1.000 0.001 0.007 0.001 0.007 OTU 12 0.51 0.74 0.06 0.08 0.06 0.09 0.05 0.05 0.056 0.159 0.929 0.989 0.062 0.168 0.796 0.949 OTU 28 1.19 1.20 0.20 0.21 0.00 0.00 0.00 0.00 0.015 0.060 0.016 0.060 0.001 0.007 0.001 0.007 OTU 37 0.14 0.27 0.01 0.02 0.35 0.18 0.51 0.27 0.074 0.178 0.077 0.178 0.207 0.394 0.001 0.007 OTU 40 0.07 0.08 1.35 0.83 0.01 0.01 0.00 0.01 0.001 0.007 0.881 0.987 0.008 0.041 0.001 0.007 OTU 3 11.02 13.33 29.61 19.69 0.52 0.56 0.41 0.45 0.067 0.173 0.865 0.986 0.004 0.023 0.001 0.007 OTU 26 0 0 0.01 0.05 0.01 0.01 0.01 0.01 0.542 0.791 0.801 0.949 0.070 0.176 0.990 1.000 OTU 19 0.14 0.29 0.31 0.24 3.24 7.48 2.09 5.77 0.372 0.613 0.614 0.823 0.107 0.223 0.441 0.700 OTU 44 0.43 1.20 0.07 0.12 0.49 0.94 1.06 2.17 0.594 0.809 0.574 0.791 0.552 0.791 0.014 0.059 OTU 39 0.02 0.05 0.13 0.20 0.59 0.79 1.02 1.34 0.072 0.178 0.318 0.539 0.001 0.007 0.016 0.060 OTU 29 0.30 0.66 0.01 0.03 3.92 6.25 0.38 0.51 0.052 0.152 0.049 0.146 0.036 0.115 0.005 0.028 OTU 2 19.98 22.32 23.46 10.10 0.85 1.46 0.19 0.30 0.834 0.975 0.285 0.493 0.002 0.012 0.001 0.007 OTU 38 0 0.01 0 0 0 0 0 0 0.690 0.012 OTU 42 0 0 0 0 0 0 0 0 OTU 17 0.62 1.33 0.25 0.31 4.45 6.58 0.12 0.18 0.451 0.703 0.002 0.012 0.091 0.201 0.531 0.785 OTU 1 0.11 0.18 0.81 1.36 0.28 0.40 0.19 0.36 0.145 0.292 0.760 0.927 0.280 0.491 0.255 0.455 OTU 11 1.09 1.39 0.10 0.10 2.01 2.44 2.31 3.56 0.026 0.086 0.761 0.927 0.907 0.987 0.007 0.038 OTU 4 3.43 6.60 0.13 0.11 12.51 8.03 16.82 10.92 0.154 0.303 0.162 0.315 0.016 0.060 0.001 0.007 OTU 48 0.41 1.14 0.01 0.02 2.29 7.23 0.38 1.17 0.225 0.414 0.747 0.927 0.817 0.962 0.222 0.413 OTU 14 0.24 0.65 0.07 0.07 0.45 0.84 1.41 2.08 0.364 0.606 0.122 0.251 0.619 0.824 0.076 0.178 OTU 46 0.21 0.60 0.01 0.02 0.49 0.81 0.52 0.87 0.306 0.524 0.757 0.927 0.396 0.646 0.016 0.060 OTU 31 0.03 0.06 0.03 0.04 0.37 0.52 0.08 0.07 0.955 0.989 0.057 0.159 0.012 0.055 0.019 0.068 OTU 45 0 0 0 0 0 0 0 0 1.000 1.000 0.281 0.491 OTU 10 0.26 0.82 0.09 0.12 0.29 0.57 0.22 0.30 0.960 0.989 0.896 0.987 0.891 0.987 0.175 0.336 OTU 32 2.90 3.72 3.80 3.98 0.18 0.46 0.05 0.11 0.872 0.986 0.567 0.791 0.004 0.023 0.001 0.007 OTU 8 1.21 2.88 0.05 0.09 7.75 7.99 6.25 8.70 0.036 0.115 0.917 0.989 0.021 0.073 0.001 0.007 OTU 6 0.82 1.99 0.10 0.13 4.11 2.46 1.24 1.97 0.455 0.703 0.026 0.086 0.019 0.068 0.001 0.007 OTU 36 0.21 0.40 0.23 0.21 0.34 0.37 0.19 0.22 0.893 0.987 0.441 0.700 0.473 0.724 0.871 0.986 OTU 35 0 0 0 0 0 0 0 0 OTU 7 0.24 0.40 0.08 0.17 4.65 13.62 6.23 18.65 0.095 0.205 0.692 0.880 0.501 0.760 0.062 0.168 OTU 16 0.19 0.27 0.29 0.47 1.37 1.80 1.55 1.94 0.776 0.932 0.653 0.862 0.074 0.178 0.048 0.146 OTU 27 0 0 0 0 0 0 0 0 OTU 20 0.22 0.67 0.03 0.05 4.32 13.62 0.62 1.88 0.849 0.986 0.770 0.932 0.576 0.791 0.424 0.686 OTU 50 0.10 0.17 1.20 0.73 0.01 0.01 0.01 0.01 0.001 0.007 0.979 1.000 0.013 0.056 0.001 0.007 OTU 22 0.14 0.42 0 0 2.08 5.32 3.60 9.82 0.107 0.223 0.671 0.877 0.236 0.430 0.001 0.007 OTU 47 0.03 0.06 0.01 0.01 0.20 0.10 0.31 0.23 0.244 0.440 0.092 0.201 0.001 0.007 0.001 0.007 OTU 41 0.99 2.99 0 0 0.50 0.87 1.28 3.32 0.723 0.913 0.923 0.989 OTU 23 0.63 1.18 0.02 0.02 2.39 2.31 2.88 2.65 0.124 0.252 0.448 0.703 0.064 0.168 0.001 0.007 OTU 43 8.90 28.14 0 0 0 0 0 0 OTU 34 0.02 0.05 0 0 0.85 0.79 1.54 1.09 0.148 0.294 0.068 0.173 0.001 0.007 0.001 0.007 OTU 24 0 0 0.05 0.07 0.15 0.13 0.12 0.11 0.674 0.877 0.082 0.187 a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. The OTUs and species abundances sorted by gut sites of the infected birds compared with the control birds are shown in the heatmaps (Figure 2). Interestingly, in the infected birds, the abundance of E. coli and Eubacterium desmolans (best type strain hits) were lower at different gut sites (Figure 3A). On the contrary, Clostridium spp. abundance was higher in the infected birds compared with the negative controls (Figure 3B). Figure 2 Heatmap showing the relative abundances (%) of the 50 most-abundant OTUs sorted by gut sites of the infected birds compared with the controls at the two sampling points post infection. The heat map integrates relative abundance of a given phylotype. Colour scaling is ranged from 0 to ≥ 25%. n.d, not detected. Figure 3 Relative abundances (%) of the most relevant OTUs in the infected birds compared with the controls at the two sampling points post infection (A) OTUs 1 and 12, (B) OTUs 4 and 29. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. Assessment of the microbial community diversity Diversity indices estimating species richness and evenness for birds are shown in Figure 4. Diversity indices indicated that microbial richness and diversity increased with age. Interestingly, diversity indices were not different comparing samples from days 1 and 7. However, older chickens (14–28 days of age) had a significantly more diverse microbial community structure as indicated by the number of OTUs observed (Sobs), Chao1, ACE, Shannon's index, and Simpson index (P < 0.01). In addition, the microbial diversity in older chickens is more consistent, as there was no difference in diversity indices comparing samples from days 14 to 28. The results also revealed significant differences in the microbial diversity among jejunum and cecum as the chicken aged, supported by Sobs (P < 0.001), Chao1 (P < 0.001), ACE (P < 0.001), Shannon's index (P < 0.001), and Simpson index (P = 0.060) with a more complex diversity in the cecum compared with the jejunum. Furthermore, a difference in species richness among the luminal and mucosa-associated gut microbiota, independent of the age, was detected in all birds as supported by Sobs (P = 0.017), Chao1 (P = 0.015), ACE (P = 0.022), respectively. Figure 4 Species richness and diversity measures of the microbial community at all gut sites in the control (A), infected birds (B), and (C) species richness and diversity estimates for bacteria from cecum content of the infected birds compared with the controls. Left Y-axis for number of observed OTUs (Sobs), Chao 1 and ACE, and Right Y-axis for Shannon and Simpson. Significant differences were calculated with Kruskal-Wallis-tests and Mann-Whitney-tests, and significance was declared at P < 0.05. Data are presented as the mean values and SD. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. In the infected birds, significant differences in the microbial diversity among jejunum and cecum supported by Sobs (P < 0.001), Chao1 (P < 0.001), ACE (P < 0.001), Shannon's index (P < 0.001), and Simpson index (P = 0.011) were found. Additionally, an increase in the species richness among luminal and mucosa-associated gut microbiota of the infected birds at 14 dpi compared with those from 7 dpi was obtained. Diversity indices were not significantly different among the gut sites of infected and control birds. Exceptional to this, a higher species richness was noticed in the cecum content of infected birds at 14 dpi, supported by Sobs, Chao1, and ACE (P = 0.047, Figure 4C), indicating that the Campylobacter infection increased the microbiota complexity. Similarity and stability of the gut microbiota composition over time The microbial community similarity among all samples over time was assessed by calculating a Bray-Curtis similarity matrix. Community similarity analysis based on the Bray-Curtis index showed clear differences between gut sites and age, indicating strong shifts in microbial community structures (Figure 5). In addition, the Bray-Curtis index suggested that the birds at the first day of age displayed a high degree of dissimilarity compared with the other ages. It was also apparent that microbiota compositions of older birds were more similar compared with young birds. Figure 5 Microbial community similarity between all samples calculated with Bray-Curtis similarities, which displays the similarity results between the control and infected groups according to age and gut sites. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. The Bray-Curtis index revealed clear differences between jejunum and cecum from infected birds at the two sampling time points post infection. Furthermore, the comparison of the microbiota between control and infected birds showed that community structures were more dissimilar at the OTUs level, demonstrating that the gut microbial communities changed as a result of infection. To measure the similarity between microbial communities in all birds at different ages, principal component analysis (PCA) was performed (Figure 6). PCA analysis showed that there was a clear clustering of the birds at days 1 and 7 of age in the jejunum and cecum compared with the other days. In addition, the microbial community of the older chickens clustered with less variation compared to young birds. PCA plots also demonstrate that, the microbial community was more separated in the ceca than in the jejunum. Figure 6 Principal component analysis (PCA) was analyzed for the control (A) and infected birds (B). Orange (day 1), Red (day 7), Green (day 14), Blue (day 21), and Black (day 28). Each symbol indicates an individual bird. All PCA plots include the data of all samples; symbols not belonging to the sample group indicated in the header are displayed faded. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. To delineate the shared species among the groups, a Venn diagram displaying the overlaps between gut sites at different ages and groups was performed (Figure S3). The proportions of shared OTUs appear to be low at each gut site from day 1 to day 28 of age. These shared species, however, varied from one site to another. Furthermore, the analysis showed that only 399 OTUs (n = 1847 OTUs) were shared among the jejunal mucosa in the control and infected birds, while 745 OTUs (n = 2401 OTUs) were shared between the jejunal content in the control and infected birds at the two time points post infection (Figure 7A). In the cecal mucosa and the cecal content, the comparison revealed that only 2218 OTUs (n = 6736 OTUs) and 2617 OTUs (n = 6860 OTUs) were shared, among control and infected birds combining the two time points post infection (Figure 7B). These data demonstrated that 25–36% of the observed OTUs in the jejunum and cecum were shared between the control and infected birds, respectively. Figure 7 Venn diagrams showing the shared OTUs between the control and infected birds at different gut sites at the two sampling points post infection (A) jejunum; (B) cecum. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i); d, day. |
title | Results |
sec | Sequence analysis, phylum and OTU classification Sequencing of 130 samples yielded 51,825,306 quality-controlled sequences, clustering into 8285 operational taxonomic units (OTUs; 0.03 distance level). Throughout all gut sites 24 phyla were identified with Firmicutes, Proteobacteria, and Tenericutes being the most abundant ones. In Figure S1A, Tables S1A–D, relative abundances of all phyla are delineated with respect to age and groups. The results showed that in the jejunum and cecum, Firmicutes and Proteobacteria were the dominating luminal and mucosal-associated phyla in all birds investigated (Tables S2, S3). At the first day of life Proteobacteria were significantly higher in the jejunal (P = 0.0000, q = 0.0000) and cecal (P = 0.016; q = 0.059) mucosa of the birds and decreased thereafter, as no significant differences were found between samples from day 14 to day 28 of age (P = 0.140; q = 0.438 and P = 0.519; q = 0.955). On the contrary, Firmicutes were significantly lower at day 1 and increased thereafter (P = 0.001; q = 0.016 and P = 0.006; q = 0.055 in the jejunal and cecal mucosa, respectively). For infected birds, relative abundances of bacterial phyla at the two sampling time points carried out post infection are represented in Figure S1B, Tables S4A–D. Figure 1 shows that the phylum Proteobacteria decreased while Firmicutes increased at either 21 (7 dpi) or 28 days of age (14 dpi). There was a significant decrease in Actinobacteria and Proteobacteria in the jejunal mucosa at 14 dpi (P = 0.006; q = 0.100 and P = 0.005; q = 0.100), while Firmicutes and Bacteroidetes were more abundant in the infected birds compared to the controls (P = 0.005; q = 0.100 and P = 0.023; q = 0.217, Table S4A). However, in the cecal content and cecal mucosa, Bacteroidetes (P = 0.001; q = 0.019) increased at 7 dpi, but decreased (P = 0.002; q = 0.026 and P = 0.005; q = 0.048) at 14 dpi in the infected birds compared with the controls, indicating that the Campylobacter infection modulates the jejunal and cecal phylum abundances in different ways. Figure 1 Relative abundances (%) of the most abundant phyla in the infected birds compared with the controls at the two sampling points post infection of (A) jejunum and (B) cecum. Data are presented as the mean values and standard deviation (SD). JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i). In Table 1, the 50 most abundant OTUs from all birds are listed including the internal OTU number, relative abundance together with the reference strain and similarity (compared with strains of the Greengenes database). Relative OTUs abundances at different ages in all birds are shown in Tables S5A–D, S6A–D. The OTUs and species abundances sorted by age at the four gut sites of the birds are shown in the heatmaps of Figure S2. In total, the 50 most abundant OTUs accounted for 73.9% of all sequences and of those 42 OTUs differed significantly in their relative abundances over all gut sites independent of the age (Tables 2, 3). At the first day of age, a notable high relative abundance of OTU 1, 25, 27, and 35 (best type strain hits: Escherichia coli, Enterococcus faecalis, Clostridium paraputrificum, and Clostridium sartagoforme) were found in both jejunal and cecal mucosa (Tables S5A,C), whereas OTU 38 (best type strain hit: Acinetobacter johnsonii) was only abundant in the jejunal mucosa and OTU 42 (best type strain hit: C. paraputrificum) was only abundant in the cecal mucosa. All these abundant OTUs decreased by age. In the jejunal mucosa, OTU 1 was the most abundant (57.9%), followed by the other four OTUs which ranged between 2.6 and 7.9%. Similarly, in the mucosa of the cecum, OTU 1 was highly abundant (65.9%), followed by OTUs 27, 25, 35, and 42 which ranged between 7.8 and 3.3%. Table 1 The 50 most abundant OTUs retrieved from different gut sites from all birds independent of the infection status. OTUs No. of sequences Relative abundance (%) Best type strain hita Similarity (%) OTU 1 642068 10.64 Escherichia coli (GU968184.1) 100 OTU 2 341923 5.66 Lactobacillus johnsonii (HM772969.1) 100 OTU 3 339288 5.62 Lactobacillus salivarius (NZ_AEBA01000145.1) 100 OTU 4 310060 5.14 Clostridium spp. (FJ808599.1) 87 OTU 5 273783 4.54 Enterococcus durans (FJ917726.1) 100 OTU 6 209121 3.46 Anaerotruncus colihominis (NR_027558.1) 100 OTU 7 208070 3.45 Eubacterium desmolans (L34618.1) 98 OTU 8 161864 2.68 Clostridium cellulolyticum (X71847.1) 87 OTU 9 157466 2.61 Spiroplasma lampyridicola (AY189134.1) 82 OTU 10 151864 2.52 Clostridium leptum (AJ305238.1) 97 OTU 11 130587 2.16 Eubacterium desmolans (L34618.1) 99 OTU 12 127446 2.11 Eubacterium desmolans (L34618.1) 98 OTU 13 120732 2.00 Clostridium papyrosolvens (NR_026102.1) 87 OTU 14 113436 1.88 Eubacterium coprostanoligenes (HM037995.1) 92 OTU 15 98491 1.63 Clostridium straminisolvens (NR_024829.1); Clostridium thermocellum (AB558166.1) 87 OTU 16 87863 1.46 Clostridium cellulolyticum (NC_011898.1) 87 OTU 17 70842 1.17 Bacillus subtilis (FJ608705.1) 94 OTU 18 67038 1.11 Lactobacillus reuteri (EU547311.1) 99 OTU 19 66212 1.10 Ruminococcus bromii (NR_025930.1) 94 OTU 20 65592 1.09 Eubacterium desmolans (L34618.1) 95 OTU 21 53133 0.88 Clostridium cellulolyticum (NC_011898.1); Clostridium papyrosolvens (NR_026102.1) 87 OTU 22 49736 0.82 Clostridium thermocellum (AB558166.1) 85 OTU 23 47570 0.79 Clostridium thermosuccinogenes (Y18180.1); Clostridium thermocellum (AB558166.1) 86 OTU 24 40373 0.67 Clostridium leptum (AJ305238.1) 95 OTU 25 36925 0.61 Enterococcus faecalis (FJ607291.1) 100 OTU 26 35311 0.58 Proteus mirabilis (GU477712.1) 100 OTU 27 31154 0.52 Clostridium paraputrificum (AY442815.1) 100 OTU 28 29186 0.48 Variovorax paradoxus (HQ005421.1) 100 OTU 29 28876 0.48 Campylobacter subsp. jejuni (NC_008787.1) 100 OTU 30 27988 0.46 Clostridium leptum (AJ305238.1) 93 OTU 31 23587 0.39 Anaerotruncus colihominis (NR_027558.1) 93 OTU 32 23559 0.39 Lactobacillus crispatus (FN692037.1) 100 OTU 33 22863 0.38 Phyllobacterium myrsinacearum (AY785330.1) 100 OTU 34 21547 0.36 Catabacter hongkongensis (AY574991.1); Clostridium thermosuccinogenes (Y18180.1) 86 OTU 35 20378 0.34 Clostridium sartagoforme (FJ384380.1) 100 OTU 36 18849 0.31 Acetivibrio cellulolyticus (L35515.1) 95 OTU 37 18055 0.30 Clostridium papyrosolvens (NR_026102.1) 86 OTU 38 17890 0.30 Acinetobacter johnsonii (EU977694.1) 100 OTU 39 15658 0.26 Clostridium papyrosolvens (NR_026102.1) 87 OTU 40 15361 0.25 Lactobacillus johnsonii (EU381128.1) 96 OTU 41 15143 0.25 Clostridium thermosuccinogenes (Y18180.1) 87 OTU 42 14985 0.25 Clostridium paraputrificum (AY442815.1) 100 OTU 43 14682 0.24 Marinobacter sp. (FJ889664.1) 99 OTU 44 14652 0.24 Clostridium papyrosolvens (NR_026102.1) 87 OTU 45 14304 0.24 Shigella flexneri (CP000266.1) 99 OTU 46 13619 0.23 Clostridium cellulolyticum (NC_011898.1) 86 OTU 47 13307 0.22 Clostridium papyrosolvens (NR_026102.1) 86 OTU 48 13152 0.22 Clostridium papyrosolvens (NR_026102.1) 87 OTU 49 12978 0.21 Clostridium papyrosolvens (NR_026102.1) 87 OTU 50 12418 0.21 Lactobacillus salivarius (NZ_AEBA01000145.1) 98 a Greengenes best type strain hit accession numbers are listed in parenthesis. Table 2 Relative abundances (%) of the most abundant OTUs in different gut sites of control birds (day 1–28). OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa OTU 49 0 0.02 0.05 0.11 0.01 0.02 0.01 0.02 0.056 0.164 0.655 0.858 0.366 0.623 0.133 0.326 OTU 25 1.89 4.01 0.06 0.07 1.05 2.95 0.01 0.02 0.001 0.011 0.015 0.067 0.365 0.623 0.001 0.011 OTU 5 12.41 25.84 13.09 21.85 0.28 0.56 0.07 0.09 0.920 0.990 0.039 0.134 0.002 0.017 0.001 0.011 OTU 30 0.45 1.45 0.40 0.72 0.74 1.11 1.25 2.09 0.913 0.990 0.385 0.643 0.808 0.946 0.059 0.170 OTU 9 0.90 2.72 1.03 3.05 3.56 9.78 5.82 15.04 0.938 0.990 0.514 0.765 0.196 0.401 0.091 0.244 OTU 13 1.34 5.22 0.75 1.84 1.36 4.51 1.41 4.43 0.714 0.890 0.831 0.946 0.940 0.990 0.549 0.770 OTU 15 0.07 0.20 0.13 0.32 1.17 1.98 4.21 9.38 0.792 0.942 0.095 0.250 0.005 0.030 0.001 0.011 OTU 18 2.36 8.46 2.34 6.03 0.08 0.23 0.03 0.09 0.961 0.994 0.409 0.665 0.081 0.220 0.013 0.059 OTU 21 0.65 2.01 0.32 0.87 0.53 1.11 1.08 3.21 0.588 0.787 0.599 0.796 0.812 0.946 0.294 0.526 OTU 33 0.96 1.38 2.57 5.92 0 0 0 0 0.341 0.603 0.001 0.011 OTU 12 0.95 2.20 1.25 4.71 2.42 5.21 5.41 11.82 0.776 0.929 0.285 0.519 0.491 0.739 0.131 0.326 OTU 28 3.21 7.19 2.99 7.77 0 0 0 0 0.941 0.990 0.006 0.034 0.001 0.011 0.001 0.011 OTU 37 0.12 0.56 0 0.01 0.39 1.93 0.07 0.28 0.140 0.326 0.939 0.990 0.947 0.991 0.177 0.379 OTU 40 0.05 0.11 1.08 1.53 0 0 0.10 0.44 0.001 0.011 0.464 0.722 0.001 0.011 0.008 0.043 OTU 3 10.36 20.66 18.43 23.28 0.39 0.63 1.52 5.30 0.252 0.475 0.517 0.765 0.001 0.011 0.002 0.017 OTU 26 0.03 0.07 0.03 0.06 1.34 2.35 1.75 3.25 0.483 0.737 0.691 0.875 0.001 0.011 0.003 0.020 OTU 19 0.80 1.99 0.22 0.57 1.09 2.22 1.01 2.17 0.189 0.395 0.979 0.997 0.961 0.994 0.134 0.326 OTU 44 0.04 0.15 0.02 0.04 0.06 0.12 0.07 0.14 0.748 0.908 0.660 0.858 0.452 0.715 0.052 0.155 OTU 39 0.02 0.07 0.01 0.02 0.07 0.20 0.08 0.19 0.769 0.927 0.726 0.893 0.253 0.475 0.046 0.147 OTU 29 0 0 0 0 0 0 0 0 0.002 0.017 OTU 2 10.86 14.76 24.38 24.19 0.13 0.26 0.31 1.13 0.046 0.147 0.817 0.946 0.001 0.011 0.001 0.011 OTU 38 1.51 5.31 0.17 0.67 0 0 0 0 0.145 0.326 0.002 0.017 OTU 42 0.51 1.20 0.01 0.03 0.67 1.71 0.01 0.03 0.012 0.057 0.041 0.136 0.717 0.890 0.669 0.864 OTU 17 0.46 1.30 0.02 0.05 2.79 7.57 0.05 0.15 0.041 0.136 0.063 0.176 0.243 0.466 0.571 0.770 OTU 1 14.87 24.08 5.33 7.93 22.17 26.59 13.03 17.69 0.069 0.190 0.231 0.452 0.295 0.526 0.062 0.176 OTU 11 0.69 1.32 0.51 0.97 2.63 7.62 3.10 5.11 0.362 0.623 0.692 0.875 0.458 0.719 0.003 0.020 OTU 4 0.51 2.00 0.17 0.56 1.34 4.60 2.14 7.58 0.571 0.770 0.611 0.806 0.525 0.770 0.147 0.326 OTU 48 0 0 0 0 0 0 0 0 0.036 0.131 OTU 14 0.24 0.69 0.22 0.43 3.77 8.30 4.66 10.97 0.542 0.770 0.747 0.908 0.023 0.091 0.004 0.025 OTU 46 0 0.02 0.01 0.02 0.26 0.65 0.25 0.50 0.348 0.609 0.991 1.000 0.028 0.106 0.039 0.134 OTU 31 0.23 0.55 0.05 0.12 0.87 1.67 0.33 0.51 0.137 0.326 0.170 0.368 0.166 0.364 0.016 0.068 OTU 45 0.05 0.09 0.01 0.01 0.35 0.56 1.02 1.62 0.023 0.091 0.096 0.250 0.016 0.068 0.004 0.025 OTU 10 0.37 1.03 0.20 0.46 4.39 11.22 4.97 10.40 0.477 0.736 0.824 0.946 0.013 0.059 0.003 0.020 OTU 32 0.12 0.43 0.23 0.79 0 0 0 0 0.540 0.770 0.868 0.975 0.012 0.057 0.006 0.034 OTU 8 0.28 1.29 0.03 0.10 1.43 5.01 2.34 7.10 0.537 0.770 0.551 0.770 0.370 0.624 0.138 0.326 OTU 6 1.17 3.54 0.13 0.28 9.20 15.81 1.39 1.56 0.238 0.461 0.007 0.039 0.021 0.087 0.001 0.011 OTU 36 0.03 0.11 0.11 0.22 0.68 1.66 0.25 0.49 0.144 0.326 0.263 0.488 0.003 0.020 0.220 0.445 OTU 35 0.57 1.28 0.02 0.04 0.90 2.13 0.02 0.08 0.012 0.057 0.034 0.126 0.542 0.770 0.867 0.975 OTU 7 1.07 2.73 1.41 2.66 3.52 7.28 6.47 12.19 0.832 0.946 0.282 0.518 0.125 0.320 0.037 0.132 OTU 16 0.73 3.50 0.27 1.01 1.41 3.77 1.96 4.92 0.905 0.990 0.562 0.770 0.400 0.656 0.146 0.326 OTU 27 0.98 2.31 0.02 0.07 1.56 4.02 0.01 0.05 0.012 0.057 0.048 0.151 0.563 0.770 0.719 0.890 OTU 20 1.68 4.52 0.05 0.18 0.86 4.28 0.91 4.07 0.049 0.151 0.981 0.997 0.448 0.715 0.997 1.000 OTU 50 0.09 0.15 0.84 0.95 0 0.01 0.06 0.23 0.001 0.011 0.486 0.737 0.001 0.011 0.002 0.017 OTU 22 0 0 0 0.02 0 0 0 0.01 0.231 0.452 0.882 0.985 OTU 47 0.12 0.53 0 0.02 0.32 1.55 0.06 0.22 0.191 0.395 0.917 0.990 0.933 0.990 0.180 0.381 OTU 41 0 0.01 0 0 0 0 0 0 0.228 0.452 1.000 1.000 OTU 23 0.12 0.50 0.01 0.02 0.07 0.20 0.09 0.23 0.136 0.326 0.682 0.874 0.819 0.946 0.024 0.093 OTU 43 0.01 0.03 0 0 0 0 0 0 OTU 34 0.03 0.14 0 0 0.06 0.16 0.14 0.38 0.903 0.990 0.417 0.672 0.390 0.645 0.051 0.155 OTU 24 0.11 0.52 0.18 0.39 1.18 1.89 1.10 1.90 0.567 0.770 0.973 0.997 0.001 0.011 0.003 0.020 a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. Table 3 Relative abundances (%) of the most abundant OTUs in different gut sites of infected birds (days 21 and 28). OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa OTU 49 0.18 0.28 0.43 0.98 0.61 1.44 0.52 0.91 0.689 0.880 0.936 0.989 0.550 0.791 0.516 0.776 OTU 25 0.02 0.04 0.08 0.09 0.00 0.00 0 0 0.077 0.178 0.063 0.168 OTU 5 1.65 2.21 8.89 6.18 0.01 0.01 0 0 0.009 0.043 0.761 0.927 0.001 0.007 0.001 0.007 OTU 30 0.31 0.94 0.06 0.08 0.30 0.38 0.16 0.12 0.957 0.989 0.355 0.596 1.000 1.000 0.013 0.056 OTU 9 0.17 0.39 0.14 0.14 1.47 4.29 2.06 5.88 0.903 0.987 0.575 0.791 0.530 0.785 0.217 0.408 OTU 13 0.64 1.06 0.72 1.35 2.87 3.77 2.65 2.58 0.955 0.989 0.950 0.989 0.056 0.159 0.020 0.071 OTU 15 0.08 0.13 0.01 0.02 1.24 0.89 2.13 1.23 0.049 0.146 0.040 0.126 0.001 0.007 0.001 0.007 OTU 18 4.67 9.39 6.34 11.77 0.19 0.44 0.14 0.36 0.572 0.791 0.857 0.986 0.102 0.218 0.011 0.051 OTU 21 0.28 0.58 0.16 0.19 1.63 2.60 1.93 2.41 0.565 0.791 0.611 0.611 0.085 0.191 0.009 0.043 OTU 33 1.11 1.14 0.13 0.13 0.00 0.00 0.00 0.00 0.008 0.041 1.000 1.000 0.001 0.007 0.001 0.007 OTU 12 0.51 0.74 0.06 0.08 0.06 0.09 0.05 0.05 0.056 0.159 0.929 0.989 0.062 0.168 0.796 0.949 OTU 28 1.19 1.20 0.20 0.21 0.00 0.00 0.00 0.00 0.015 0.060 0.016 0.060 0.001 0.007 0.001 0.007 OTU 37 0.14 0.27 0.01 0.02 0.35 0.18 0.51 0.27 0.074 0.178 0.077 0.178 0.207 0.394 0.001 0.007 OTU 40 0.07 0.08 1.35 0.83 0.01 0.01 0.00 0.01 0.001 0.007 0.881 0.987 0.008 0.041 0.001 0.007 OTU 3 11.02 13.33 29.61 19.69 0.52 0.56 0.41 0.45 0.067 0.173 0.865 0.986 0.004 0.023 0.001 0.007 OTU 26 0 0 0.01 0.05 0.01 0.01 0.01 0.01 0.542 0.791 0.801 0.949 0.070 0.176 0.990 1.000 OTU 19 0.14 0.29 0.31 0.24 3.24 7.48 2.09 5.77 0.372 0.613 0.614 0.823 0.107 0.223 0.441 0.700 OTU 44 0.43 1.20 0.07 0.12 0.49 0.94 1.06 2.17 0.594 0.809 0.574 0.791 0.552 0.791 0.014 0.059 OTU 39 0.02 0.05 0.13 0.20 0.59 0.79 1.02 1.34 0.072 0.178 0.318 0.539 0.001 0.007 0.016 0.060 OTU 29 0.30 0.66 0.01 0.03 3.92 6.25 0.38 0.51 0.052 0.152 0.049 0.146 0.036 0.115 0.005 0.028 OTU 2 19.98 22.32 23.46 10.10 0.85 1.46 0.19 0.30 0.834 0.975 0.285 0.493 0.002 0.012 0.001 0.007 OTU 38 0 0.01 0 0 0 0 0 0 0.690 0.012 OTU 42 0 0 0 0 0 0 0 0 OTU 17 0.62 1.33 0.25 0.31 4.45 6.58 0.12 0.18 0.451 0.703 0.002 0.012 0.091 0.201 0.531 0.785 OTU 1 0.11 0.18 0.81 1.36 0.28 0.40 0.19 0.36 0.145 0.292 0.760 0.927 0.280 0.491 0.255 0.455 OTU 11 1.09 1.39 0.10 0.10 2.01 2.44 2.31 3.56 0.026 0.086 0.761 0.927 0.907 0.987 0.007 0.038 OTU 4 3.43 6.60 0.13 0.11 12.51 8.03 16.82 10.92 0.154 0.303 0.162 0.315 0.016 0.060 0.001 0.007 OTU 48 0.41 1.14 0.01 0.02 2.29 7.23 0.38 1.17 0.225 0.414 0.747 0.927 0.817 0.962 0.222 0.413 OTU 14 0.24 0.65 0.07 0.07 0.45 0.84 1.41 2.08 0.364 0.606 0.122 0.251 0.619 0.824 0.076 0.178 OTU 46 0.21 0.60 0.01 0.02 0.49 0.81 0.52 0.87 0.306 0.524 0.757 0.927 0.396 0.646 0.016 0.060 OTU 31 0.03 0.06 0.03 0.04 0.37 0.52 0.08 0.07 0.955 0.989 0.057 0.159 0.012 0.055 0.019 0.068 OTU 45 0 0 0 0 0 0 0 0 1.000 1.000 0.281 0.491 OTU 10 0.26 0.82 0.09 0.12 0.29 0.57 0.22 0.30 0.960 0.989 0.896 0.987 0.891 0.987 0.175 0.336 OTU 32 2.90 3.72 3.80 3.98 0.18 0.46 0.05 0.11 0.872 0.986 0.567 0.791 0.004 0.023 0.001 0.007 OTU 8 1.21 2.88 0.05 0.09 7.75 7.99 6.25 8.70 0.036 0.115 0.917 0.989 0.021 0.073 0.001 0.007 OTU 6 0.82 1.99 0.10 0.13 4.11 2.46 1.24 1.97 0.455 0.703 0.026 0.086 0.019 0.068 0.001 0.007 OTU 36 0.21 0.40 0.23 0.21 0.34 0.37 0.19 0.22 0.893 0.987 0.441 0.700 0.473 0.724 0.871 0.986 OTU 35 0 0 0 0 0 0 0 0 OTU 7 0.24 0.40 0.08 0.17 4.65 13.62 6.23 18.65 0.095 0.205 0.692 0.880 0.501 0.760 0.062 0.168 OTU 16 0.19 0.27 0.29 0.47 1.37 1.80 1.55 1.94 0.776 0.932 0.653 0.862 0.074 0.178 0.048 0.146 OTU 27 0 0 0 0 0 0 0 0 OTU 20 0.22 0.67 0.03 0.05 4.32 13.62 0.62 1.88 0.849 0.986 0.770 0.932 0.576 0.791 0.424 0.686 OTU 50 0.10 0.17 1.20 0.73 0.01 0.01 0.01 0.01 0.001 0.007 0.979 1.000 0.013 0.056 0.001 0.007 OTU 22 0.14 0.42 0 0 2.08 5.32 3.60 9.82 0.107 0.223 0.671 0.877 0.236 0.430 0.001 0.007 OTU 47 0.03 0.06 0.01 0.01 0.20 0.10 0.31 0.23 0.244 0.440 0.092 0.201 0.001 0.007 0.001 0.007 OTU 41 0.99 2.99 0 0 0.50 0.87 1.28 3.32 0.723 0.913 0.923 0.989 OTU 23 0.63 1.18 0.02 0.02 2.39 2.31 2.88 2.65 0.124 0.252 0.448 0.703 0.064 0.168 0.001 0.007 OTU 43 8.90 28.14 0 0 0 0 0 0 OTU 34 0.02 0.05 0 0 0.85 0.79 1.54 1.09 0.148 0.294 0.068 0.173 0.001 0.007 0.001 0.007 OTU 24 0 0 0.05 0.07 0.15 0.13 0.12 0.11 0.674 0.877 0.082 0.187 a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. The OTUs and species abundances sorted by gut sites of the infected birds compared with the control birds are shown in the heatmaps (Figure 2). Interestingly, in the infected birds, the abundance of E. coli and Eubacterium desmolans (best type strain hits) were lower at different gut sites (Figure 3A). On the contrary, Clostridium spp. abundance was higher in the infected birds compared with the negative controls (Figure 3B). Figure 2 Heatmap showing the relative abundances (%) of the 50 most-abundant OTUs sorted by gut sites of the infected birds compared with the controls at the two sampling points post infection. The heat map integrates relative abundance of a given phylotype. Colour scaling is ranged from 0 to ≥ 25%. n.d, not detected. Figure 3 Relative abundances (%) of the most relevant OTUs in the infected birds compared with the controls at the two sampling points post infection (A) OTUs 1 and 12, (B) OTUs 4 and 29. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
title | Sequence analysis, phylum and OTU classification |
p | Sequencing of 130 samples yielded 51,825,306 quality-controlled sequences, clustering into 8285 operational taxonomic units (OTUs; 0.03 distance level). Throughout all gut sites 24 phyla were identified with Firmicutes, Proteobacteria, and Tenericutes being the most abundant ones. In Figure S1A, Tables S1A–D, relative abundances of all phyla are delineated with respect to age and groups. The results showed that in the jejunum and cecum, Firmicutes and Proteobacteria were the dominating luminal and mucosal-associated phyla in all birds investigated (Tables S2, S3). |
p | At the first day of life Proteobacteria were significantly higher in the jejunal (P = 0.0000, q = 0.0000) and cecal (P = 0.016; q = 0.059) mucosa of the birds and decreased thereafter, as no significant differences were found between samples from day 14 to day 28 of age (P = 0.140; q = 0.438 and P = 0.519; q = 0.955). On the contrary, Firmicutes were significantly lower at day 1 and increased thereafter (P = 0.001; q = 0.016 and P = 0.006; q = 0.055 in the jejunal and cecal mucosa, respectively). |
p | For infected birds, relative abundances of bacterial phyla at the two sampling time points carried out post infection are represented in Figure S1B, Tables S4A–D. Figure 1 shows that the phylum Proteobacteria decreased while Firmicutes increased at either 21 (7 dpi) or 28 days of age (14 dpi). There was a significant decrease in Actinobacteria and Proteobacteria in the jejunal mucosa at 14 dpi (P = 0.006; q = 0.100 and P = 0.005; q = 0.100), while Firmicutes and Bacteroidetes were more abundant in the infected birds compared to the controls (P = 0.005; q = 0.100 and P = 0.023; q = 0.217, Table S4A). However, in the cecal content and cecal mucosa, Bacteroidetes (P = 0.001; q = 0.019) increased at 7 dpi, but decreased (P = 0.002; q = 0.026 and P = 0.005; q = 0.048) at 14 dpi in the infected birds compared with the controls, indicating that the Campylobacter infection modulates the jejunal and cecal phylum abundances in different ways. |
figure | Figure 1 Relative abundances (%) of the most abundant phyla in the infected birds compared with the controls at the two sampling points post infection of (A) jejunum and (B) cecum. Data are presented as the mean values and standard deviation (SD). JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i). |
label | Figure 1 |
caption | Relative abundances (%) of the most abundant phyla in the infected birds compared with the controls at the two sampling points post infection of (A) jejunum and (B) cecum. Data are presented as the mean values and standard deviation (SD). JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i). |
p | Relative abundances (%) of the most abundant phyla in the infected birds compared with the controls at the two sampling points post infection of (A) jejunum and (B) cecum. Data are presented as the mean values and standard deviation (SD). JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i). |
p | In Table 1, the 50 most abundant OTUs from all birds are listed including the internal OTU number, relative abundance together with the reference strain and similarity (compared with strains of the Greengenes database). Relative OTUs abundances at different ages in all birds are shown in Tables S5A–D, S6A–D. The OTUs and species abundances sorted by age at the four gut sites of the birds are shown in the heatmaps of Figure S2. In total, the 50 most abundant OTUs accounted for 73.9% of all sequences and of those 42 OTUs differed significantly in their relative abundances over all gut sites independent of the age (Tables 2, 3). At the first day of age, a notable high relative abundance of OTU 1, 25, 27, and 35 (best type strain hits: Escherichia coli, Enterococcus faecalis, Clostridium paraputrificum, and Clostridium sartagoforme) were found in both jejunal and cecal mucosa (Tables S5A,C), whereas OTU 38 (best type strain hit: Acinetobacter johnsonii) was only abundant in the jejunal mucosa and OTU 42 (best type strain hit: C. paraputrificum) was only abundant in the cecal mucosa. All these abundant OTUs decreased by age. In the jejunal mucosa, OTU 1 was the most abundant (57.9%), followed by the other four OTUs which ranged between 2.6 and 7.9%. Similarly, in the mucosa of the cecum, OTU 1 was highly abundant (65.9%), followed by OTUs 27, 25, 35, and 42 which ranged between 7.8 and 3.3%. |
table-wrap | Table 1 The 50 most abundant OTUs retrieved from different gut sites from all birds independent of the infection status. OTUs No. of sequences Relative abundance (%) Best type strain hita Similarity (%) OTU 1 642068 10.64 Escherichia coli (GU968184.1) 100 OTU 2 341923 5.66 Lactobacillus johnsonii (HM772969.1) 100 OTU 3 339288 5.62 Lactobacillus salivarius (NZ_AEBA01000145.1) 100 OTU 4 310060 5.14 Clostridium spp. (FJ808599.1) 87 OTU 5 273783 4.54 Enterococcus durans (FJ917726.1) 100 OTU 6 209121 3.46 Anaerotruncus colihominis (NR_027558.1) 100 OTU 7 208070 3.45 Eubacterium desmolans (L34618.1) 98 OTU 8 161864 2.68 Clostridium cellulolyticum (X71847.1) 87 OTU 9 157466 2.61 Spiroplasma lampyridicola (AY189134.1) 82 OTU 10 151864 2.52 Clostridium leptum (AJ305238.1) 97 OTU 11 130587 2.16 Eubacterium desmolans (L34618.1) 99 OTU 12 127446 2.11 Eubacterium desmolans (L34618.1) 98 OTU 13 120732 2.00 Clostridium papyrosolvens (NR_026102.1) 87 OTU 14 113436 1.88 Eubacterium coprostanoligenes (HM037995.1) 92 OTU 15 98491 1.63 Clostridium straminisolvens (NR_024829.1); Clostridium thermocellum (AB558166.1) 87 OTU 16 87863 1.46 Clostridium cellulolyticum (NC_011898.1) 87 OTU 17 70842 1.17 Bacillus subtilis (FJ608705.1) 94 OTU 18 67038 1.11 Lactobacillus reuteri (EU547311.1) 99 OTU 19 66212 1.10 Ruminococcus bromii (NR_025930.1) 94 OTU 20 65592 1.09 Eubacterium desmolans (L34618.1) 95 OTU 21 53133 0.88 Clostridium cellulolyticum (NC_011898.1); Clostridium papyrosolvens (NR_026102.1) 87 OTU 22 49736 0.82 Clostridium thermocellum (AB558166.1) 85 OTU 23 47570 0.79 Clostridium thermosuccinogenes (Y18180.1); Clostridium thermocellum (AB558166.1) 86 OTU 24 40373 0.67 Clostridium leptum (AJ305238.1) 95 OTU 25 36925 0.61 Enterococcus faecalis (FJ607291.1) 100 OTU 26 35311 0.58 Proteus mirabilis (GU477712.1) 100 OTU 27 31154 0.52 Clostridium paraputrificum (AY442815.1) 100 OTU 28 29186 0.48 Variovorax paradoxus (HQ005421.1) 100 OTU 29 28876 0.48 Campylobacter subsp. jejuni (NC_008787.1) 100 OTU 30 27988 0.46 Clostridium leptum (AJ305238.1) 93 OTU 31 23587 0.39 Anaerotruncus colihominis (NR_027558.1) 93 OTU 32 23559 0.39 Lactobacillus crispatus (FN692037.1) 100 OTU 33 22863 0.38 Phyllobacterium myrsinacearum (AY785330.1) 100 OTU 34 21547 0.36 Catabacter hongkongensis (AY574991.1); Clostridium thermosuccinogenes (Y18180.1) 86 OTU 35 20378 0.34 Clostridium sartagoforme (FJ384380.1) 100 OTU 36 18849 0.31 Acetivibrio cellulolyticus (L35515.1) 95 OTU 37 18055 0.30 Clostridium papyrosolvens (NR_026102.1) 86 OTU 38 17890 0.30 Acinetobacter johnsonii (EU977694.1) 100 OTU 39 15658 0.26 Clostridium papyrosolvens (NR_026102.1) 87 OTU 40 15361 0.25 Lactobacillus johnsonii (EU381128.1) 96 OTU 41 15143 0.25 Clostridium thermosuccinogenes (Y18180.1) 87 OTU 42 14985 0.25 Clostridium paraputrificum (AY442815.1) 100 OTU 43 14682 0.24 Marinobacter sp. (FJ889664.1) 99 OTU 44 14652 0.24 Clostridium papyrosolvens (NR_026102.1) 87 OTU 45 14304 0.24 Shigella flexneri (CP000266.1) 99 OTU 46 13619 0.23 Clostridium cellulolyticum (NC_011898.1) 86 OTU 47 13307 0.22 Clostridium papyrosolvens (NR_026102.1) 86 OTU 48 13152 0.22 Clostridium papyrosolvens (NR_026102.1) 87 OTU 49 12978 0.21 Clostridium papyrosolvens (NR_026102.1) 87 OTU 50 12418 0.21 Lactobacillus salivarius (NZ_AEBA01000145.1) 98 a Greengenes best type strain hit accession numbers are listed in parenthesis. |
label | Table 1 |
caption | The 50 most abundant OTUs retrieved from different gut sites from all birds independent of the infection status. |
p | The 50 most abundant OTUs retrieved from different gut sites from all birds independent of the infection status. |
table | OTUs No. of sequences Relative abundance (%) Best type strain hita Similarity (%) OTU 1 642068 10.64 Escherichia coli (GU968184.1) 100 OTU 2 341923 5.66 Lactobacillus johnsonii (HM772969.1) 100 OTU 3 339288 5.62 Lactobacillus salivarius (NZ_AEBA01000145.1) 100 OTU 4 310060 5.14 Clostridium spp. (FJ808599.1) 87 OTU 5 273783 4.54 Enterococcus durans (FJ917726.1) 100 OTU 6 209121 3.46 Anaerotruncus colihominis (NR_027558.1) 100 OTU 7 208070 3.45 Eubacterium desmolans (L34618.1) 98 OTU 8 161864 2.68 Clostridium cellulolyticum (X71847.1) 87 OTU 9 157466 2.61 Spiroplasma lampyridicola (AY189134.1) 82 OTU 10 151864 2.52 Clostridium leptum (AJ305238.1) 97 OTU 11 130587 2.16 Eubacterium desmolans (L34618.1) 99 OTU 12 127446 2.11 Eubacterium desmolans (L34618.1) 98 OTU 13 120732 2.00 Clostridium papyrosolvens (NR_026102.1) 87 OTU 14 113436 1.88 Eubacterium coprostanoligenes (HM037995.1) 92 OTU 15 98491 1.63 Clostridium straminisolvens (NR_024829.1); Clostridium thermocellum (AB558166.1) 87 OTU 16 87863 1.46 Clostridium cellulolyticum (NC_011898.1) 87 OTU 17 70842 1.17 Bacillus subtilis (FJ608705.1) 94 OTU 18 67038 1.11 Lactobacillus reuteri (EU547311.1) 99 OTU 19 66212 1.10 Ruminococcus bromii (NR_025930.1) 94 OTU 20 65592 1.09 Eubacterium desmolans (L34618.1) 95 OTU 21 53133 0.88 Clostridium cellulolyticum (NC_011898.1); Clostridium papyrosolvens (NR_026102.1) 87 OTU 22 49736 0.82 Clostridium thermocellum (AB558166.1) 85 OTU 23 47570 0.79 Clostridium thermosuccinogenes (Y18180.1); Clostridium thermocellum (AB558166.1) 86 OTU 24 40373 0.67 Clostridium leptum (AJ305238.1) 95 OTU 25 36925 0.61 Enterococcus faecalis (FJ607291.1) 100 OTU 26 35311 0.58 Proteus mirabilis (GU477712.1) 100 OTU 27 31154 0.52 Clostridium paraputrificum (AY442815.1) 100 OTU 28 29186 0.48 Variovorax paradoxus (HQ005421.1) 100 OTU 29 28876 0.48 Campylobacter subsp. jejuni (NC_008787.1) 100 OTU 30 27988 0.46 Clostridium leptum (AJ305238.1) 93 OTU 31 23587 0.39 Anaerotruncus colihominis (NR_027558.1) 93 OTU 32 23559 0.39 Lactobacillus crispatus (FN692037.1) 100 OTU 33 22863 0.38 Phyllobacterium myrsinacearum (AY785330.1) 100 OTU 34 21547 0.36 Catabacter hongkongensis (AY574991.1); Clostridium thermosuccinogenes (Y18180.1) 86 OTU 35 20378 0.34 Clostridium sartagoforme (FJ384380.1) 100 OTU 36 18849 0.31 Acetivibrio cellulolyticus (L35515.1) 95 OTU 37 18055 0.30 Clostridium papyrosolvens (NR_026102.1) 86 OTU 38 17890 0.30 Acinetobacter johnsonii (EU977694.1) 100 OTU 39 15658 0.26 Clostridium papyrosolvens (NR_026102.1) 87 OTU 40 15361 0.25 Lactobacillus johnsonii (EU381128.1) 96 OTU 41 15143 0.25 Clostridium thermosuccinogenes (Y18180.1) 87 OTU 42 14985 0.25 Clostridium paraputrificum (AY442815.1) 100 OTU 43 14682 0.24 Marinobacter sp. (FJ889664.1) 99 OTU 44 14652 0.24 Clostridium papyrosolvens (NR_026102.1) 87 OTU 45 14304 0.24 Shigella flexneri (CP000266.1) 99 OTU 46 13619 0.23 Clostridium cellulolyticum (NC_011898.1) 86 OTU 47 13307 0.22 Clostridium papyrosolvens (NR_026102.1) 86 OTU 48 13152 0.22 Clostridium papyrosolvens (NR_026102.1) 87 OTU 49 12978 0.21 Clostridium papyrosolvens (NR_026102.1) 87 OTU 50 12418 0.21 Lactobacillus salivarius (NZ_AEBA01000145.1) 98 |
tr | OTUs No. of sequences Relative abundance (%) Best type strain hita Similarity (%) |
th | OTUs |
th | No. of sequences |
th | Relative abundance (%) |
th | Best type strain hita |
th | Similarity (%) |
tr | OTU 1 642068 10.64 Escherichia coli (GU968184.1) 100 |
td | OTU 1 |
td | 642068 |
td | 10.64 |
td | Escherichia coli (GU968184.1) |
td | 100 |
tr | OTU 2 341923 5.66 Lactobacillus johnsonii (HM772969.1) 100 |
td | OTU 2 |
td | 341923 |
td | 5.66 |
td | Lactobacillus johnsonii (HM772969.1) |
td | 100 |
tr | OTU 3 339288 5.62 Lactobacillus salivarius (NZ_AEBA01000145.1) 100 |
td | OTU 3 |
td | 339288 |
td | 5.62 |
td | Lactobacillus salivarius (NZ_AEBA01000145.1) |
td | 100 |
tr | OTU 4 310060 5.14 Clostridium spp. (FJ808599.1) 87 |
td | OTU 4 |
td | 310060 |
td | 5.14 |
td | Clostridium spp. (FJ808599.1) |
td | 87 |
tr | OTU 5 273783 4.54 Enterococcus durans (FJ917726.1) 100 |
td | OTU 5 |
td | 273783 |
td | 4.54 |
td | Enterococcus durans (FJ917726.1) |
td | 100 |
tr | OTU 6 209121 3.46 Anaerotruncus colihominis (NR_027558.1) 100 |
td | OTU 6 |
td | 209121 |
td | 3.46 |
td | Anaerotruncus colihominis (NR_027558.1) |
td | 100 |
tr | OTU 7 208070 3.45 Eubacterium desmolans (L34618.1) 98 |
td | OTU 7 |
td | 208070 |
td | 3.45 |
td | Eubacterium desmolans (L34618.1) |
td | 98 |
tr | OTU 8 161864 2.68 Clostridium cellulolyticum (X71847.1) 87 |
td | OTU 8 |
td | 161864 |
td | 2.68 |
td | Clostridium cellulolyticum (X71847.1) |
td | 87 |
tr | OTU 9 157466 2.61 Spiroplasma lampyridicola (AY189134.1) 82 |
td | OTU 9 |
td | 157466 |
td | 2.61 |
td | Spiroplasma lampyridicola (AY189134.1) |
td | 82 |
tr | OTU 10 151864 2.52 Clostridium leptum (AJ305238.1) 97 |
td | OTU 10 |
td | 151864 |
td | 2.52 |
td | Clostridium leptum (AJ305238.1) |
td | 97 |
tr | OTU 11 130587 2.16 Eubacterium desmolans (L34618.1) 99 |
td | OTU 11 |
td | 130587 |
td | 2.16 |
td | Eubacterium desmolans (L34618.1) |
td | 99 |
tr | OTU 12 127446 2.11 Eubacterium desmolans (L34618.1) 98 |
td | OTU 12 |
td | 127446 |
td | 2.11 |
td | Eubacterium desmolans (L34618.1) |
td | 98 |
tr | OTU 13 120732 2.00 Clostridium papyrosolvens (NR_026102.1) 87 |
td | OTU 13 |
td | 120732 |
td | 2.00 |
td | Clostridium papyrosolvens (NR_026102.1) |
td | 87 |
tr | OTU 14 113436 1.88 Eubacterium coprostanoligenes (HM037995.1) 92 |
td | OTU 14 |
td | 113436 |
td | 1.88 |
td | Eubacterium coprostanoligenes (HM037995.1) |
td | 92 |
tr | OTU 15 98491 1.63 Clostridium straminisolvens (NR_024829.1); Clostridium thermocellum (AB558166.1) 87 |
td | OTU 15 |
td | 98491 |
td | 1.63 |
td | Clostridium straminisolvens (NR_024829.1); Clostridium thermocellum (AB558166.1) |
td | 87 |
tr | OTU 16 87863 1.46 Clostridium cellulolyticum (NC_011898.1) 87 |
td | OTU 16 |
td | 87863 |
td | 1.46 |
td | Clostridium cellulolyticum (NC_011898.1) |
td | 87 |
tr | OTU 17 70842 1.17 Bacillus subtilis (FJ608705.1) 94 |
td | OTU 17 |
td | 70842 |
td | 1.17 |
td | Bacillus subtilis (FJ608705.1) |
td | 94 |
tr | OTU 18 67038 1.11 Lactobacillus reuteri (EU547311.1) 99 |
td | OTU 18 |
td | 67038 |
td | 1.11 |
td | Lactobacillus reuteri (EU547311.1) |
td | 99 |
tr | OTU 19 66212 1.10 Ruminococcus bromii (NR_025930.1) 94 |
td | OTU 19 |
td | 66212 |
td | 1.10 |
td | Ruminococcus bromii (NR_025930.1) |
td | 94 |
tr | OTU 20 65592 1.09 Eubacterium desmolans (L34618.1) 95 |
td | OTU 20 |
td | 65592 |
td | 1.09 |
td | Eubacterium desmolans (L34618.1) |
td | 95 |
tr | OTU 21 53133 0.88 Clostridium cellulolyticum (NC_011898.1); Clostridium papyrosolvens (NR_026102.1) 87 |
td | OTU 21 |
td | 53133 |
td | 0.88 |
td | Clostridium cellulolyticum (NC_011898.1); Clostridium papyrosolvens (NR_026102.1) |
td | 87 |
tr | OTU 22 49736 0.82 Clostridium thermocellum (AB558166.1) 85 |
td | OTU 22 |
td | 49736 |
td | 0.82 |
td | Clostridium thermocellum (AB558166.1) |
td | 85 |
tr | OTU 23 47570 0.79 Clostridium thermosuccinogenes (Y18180.1); Clostridium thermocellum (AB558166.1) 86 |
td | OTU 23 |
td | 47570 |
td | 0.79 |
td | Clostridium thermosuccinogenes (Y18180.1); Clostridium thermocellum (AB558166.1) |
td | 86 |
tr | OTU 24 40373 0.67 Clostridium leptum (AJ305238.1) 95 |
td | OTU 24 |
td | 40373 |
td | 0.67 |
td | Clostridium leptum (AJ305238.1) |
td | 95 |
tr | OTU 25 36925 0.61 Enterococcus faecalis (FJ607291.1) 100 |
td | OTU 25 |
td | 36925 |
td | 0.61 |
td | Enterococcus faecalis (FJ607291.1) |
td | 100 |
tr | OTU 26 35311 0.58 Proteus mirabilis (GU477712.1) 100 |
td | OTU 26 |
td | 35311 |
td | 0.58 |
td | Proteus mirabilis (GU477712.1) |
td | 100 |
tr | OTU 27 31154 0.52 Clostridium paraputrificum (AY442815.1) 100 |
td | OTU 27 |
td | 31154 |
td | 0.52 |
td | Clostridium paraputrificum (AY442815.1) |
td | 100 |
tr | OTU 28 29186 0.48 Variovorax paradoxus (HQ005421.1) 100 |
td | OTU 28 |
td | 29186 |
td | 0.48 |
td | Variovorax paradoxus (HQ005421.1) |
td | 100 |
tr | OTU 29 28876 0.48 Campylobacter subsp. jejuni (NC_008787.1) 100 |
td | OTU 29 |
td | 28876 |
td | 0.48 |
td | Campylobacter subsp. jejuni (NC_008787.1) |
td | 100 |
tr | OTU 30 27988 0.46 Clostridium leptum (AJ305238.1) 93 |
td | OTU 30 |
td | 27988 |
td | 0.46 |
td | Clostridium leptum (AJ305238.1) |
td | 93 |
tr | OTU 31 23587 0.39 Anaerotruncus colihominis (NR_027558.1) 93 |
td | OTU 31 |
td | 23587 |
td | 0.39 |
td | Anaerotruncus colihominis (NR_027558.1) |
td | 93 |
tr | OTU 32 23559 0.39 Lactobacillus crispatus (FN692037.1) 100 |
td | OTU 32 |
td | 23559 |
td | 0.39 |
td | Lactobacillus crispatus (FN692037.1) |
td | 100 |
tr | OTU 33 22863 0.38 Phyllobacterium myrsinacearum (AY785330.1) 100 |
td | OTU 33 |
td | 22863 |
td | 0.38 |
td | Phyllobacterium myrsinacearum (AY785330.1) |
td | 100 |
tr | OTU 34 21547 0.36 Catabacter hongkongensis (AY574991.1); Clostridium thermosuccinogenes (Y18180.1) 86 |
td | OTU 34 |
td | 21547 |
td | 0.36 |
td | Catabacter hongkongensis (AY574991.1); Clostridium thermosuccinogenes (Y18180.1) |
td | 86 |
tr | OTU 35 20378 0.34 Clostridium sartagoforme (FJ384380.1) 100 |
td | OTU 35 |
td | 20378 |
td | 0.34 |
td | Clostridium sartagoforme (FJ384380.1) |
td | 100 |
tr | OTU 36 18849 0.31 Acetivibrio cellulolyticus (L35515.1) 95 |
td | OTU 36 |
td | 18849 |
td | 0.31 |
td | Acetivibrio cellulolyticus (L35515.1) |
td | 95 |
tr | OTU 37 18055 0.30 Clostridium papyrosolvens (NR_026102.1) 86 |
td | OTU 37 |
td | 18055 |
td | 0.30 |
td | Clostridium papyrosolvens (NR_026102.1) |
td | 86 |
tr | OTU 38 17890 0.30 Acinetobacter johnsonii (EU977694.1) 100 |
td | OTU 38 |
td | 17890 |
td | 0.30 |
td | Acinetobacter johnsonii (EU977694.1) |
td | 100 |
tr | OTU 39 15658 0.26 Clostridium papyrosolvens (NR_026102.1) 87 |
td | OTU 39 |
td | 15658 |
td | 0.26 |
td | Clostridium papyrosolvens (NR_026102.1) |
td | 87 |
tr | OTU 40 15361 0.25 Lactobacillus johnsonii (EU381128.1) 96 |
td | OTU 40 |
td | 15361 |
td | 0.25 |
td | Lactobacillus johnsonii (EU381128.1) |
td | 96 |
tr | OTU 41 15143 0.25 Clostridium thermosuccinogenes (Y18180.1) 87 |
td | OTU 41 |
td | 15143 |
td | 0.25 |
td | Clostridium thermosuccinogenes (Y18180.1) |
td | 87 |
tr | OTU 42 14985 0.25 Clostridium paraputrificum (AY442815.1) 100 |
td | OTU 42 |
td | 14985 |
td | 0.25 |
td | Clostridium paraputrificum (AY442815.1) |
td | 100 |
tr | OTU 43 14682 0.24 Marinobacter sp. (FJ889664.1) 99 |
td | OTU 43 |
td | 14682 |
td | 0.24 |
td | Marinobacter sp. (FJ889664.1) |
td | 99 |
tr | OTU 44 14652 0.24 Clostridium papyrosolvens (NR_026102.1) 87 |
td | OTU 44 |
td | 14652 |
td | 0.24 |
td | Clostridium papyrosolvens (NR_026102.1) |
td | 87 |
tr | OTU 45 14304 0.24 Shigella flexneri (CP000266.1) 99 |
td | OTU 45 |
td | 14304 |
td | 0.24 |
td | Shigella flexneri (CP000266.1) |
td | 99 |
tr | OTU 46 13619 0.23 Clostridium cellulolyticum (NC_011898.1) 86 |
td | OTU 46 |
td | 13619 |
td | 0.23 |
td | Clostridium cellulolyticum (NC_011898.1) |
td | 86 |
tr | OTU 47 13307 0.22 Clostridium papyrosolvens (NR_026102.1) 86 |
td | OTU 47 |
td | 13307 |
td | 0.22 |
td | Clostridium papyrosolvens (NR_026102.1) |
td | 86 |
tr | OTU 48 13152 0.22 Clostridium papyrosolvens (NR_026102.1) 87 |
td | OTU 48 |
td | 13152 |
td | 0.22 |
td | Clostridium papyrosolvens (NR_026102.1) |
td | 87 |
tr | OTU 49 12978 0.21 Clostridium papyrosolvens (NR_026102.1) 87 |
td | OTU 49 |
td | 12978 |
td | 0.21 |
td | Clostridium papyrosolvens (NR_026102.1) |
td | 87 |
tr | OTU 50 12418 0.21 Lactobacillus salivarius (NZ_AEBA01000145.1) 98 |
td | OTU 50 |
td | 12418 |
td | 0.21 |
td | Lactobacillus salivarius (NZ_AEBA01000145.1) |
td | 98 |
table-wrap-foot | a Greengenes best type strain hit accession numbers are listed in parenthesis. |
footnote | a Greengenes best type strain hit accession numbers are listed in parenthesis. |
label | a |
p | Greengenes best type strain hit accession numbers are listed in parenthesis. |
table-wrap | Table 2 Relative abundances (%) of the most abundant OTUs in different gut sites of control birds (day 1–28). OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa OTU 49 0 0.02 0.05 0.11 0.01 0.02 0.01 0.02 0.056 0.164 0.655 0.858 0.366 0.623 0.133 0.326 OTU 25 1.89 4.01 0.06 0.07 1.05 2.95 0.01 0.02 0.001 0.011 0.015 0.067 0.365 0.623 0.001 0.011 OTU 5 12.41 25.84 13.09 21.85 0.28 0.56 0.07 0.09 0.920 0.990 0.039 0.134 0.002 0.017 0.001 0.011 OTU 30 0.45 1.45 0.40 0.72 0.74 1.11 1.25 2.09 0.913 0.990 0.385 0.643 0.808 0.946 0.059 0.170 OTU 9 0.90 2.72 1.03 3.05 3.56 9.78 5.82 15.04 0.938 0.990 0.514 0.765 0.196 0.401 0.091 0.244 OTU 13 1.34 5.22 0.75 1.84 1.36 4.51 1.41 4.43 0.714 0.890 0.831 0.946 0.940 0.990 0.549 0.770 OTU 15 0.07 0.20 0.13 0.32 1.17 1.98 4.21 9.38 0.792 0.942 0.095 0.250 0.005 0.030 0.001 0.011 OTU 18 2.36 8.46 2.34 6.03 0.08 0.23 0.03 0.09 0.961 0.994 0.409 0.665 0.081 0.220 0.013 0.059 OTU 21 0.65 2.01 0.32 0.87 0.53 1.11 1.08 3.21 0.588 0.787 0.599 0.796 0.812 0.946 0.294 0.526 OTU 33 0.96 1.38 2.57 5.92 0 0 0 0 0.341 0.603 0.001 0.011 OTU 12 0.95 2.20 1.25 4.71 2.42 5.21 5.41 11.82 0.776 0.929 0.285 0.519 0.491 0.739 0.131 0.326 OTU 28 3.21 7.19 2.99 7.77 0 0 0 0 0.941 0.990 0.006 0.034 0.001 0.011 0.001 0.011 OTU 37 0.12 0.56 0 0.01 0.39 1.93 0.07 0.28 0.140 0.326 0.939 0.990 0.947 0.991 0.177 0.379 OTU 40 0.05 0.11 1.08 1.53 0 0 0.10 0.44 0.001 0.011 0.464 0.722 0.001 0.011 0.008 0.043 OTU 3 10.36 20.66 18.43 23.28 0.39 0.63 1.52 5.30 0.252 0.475 0.517 0.765 0.001 0.011 0.002 0.017 OTU 26 0.03 0.07 0.03 0.06 1.34 2.35 1.75 3.25 0.483 0.737 0.691 0.875 0.001 0.011 0.003 0.020 OTU 19 0.80 1.99 0.22 0.57 1.09 2.22 1.01 2.17 0.189 0.395 0.979 0.997 0.961 0.994 0.134 0.326 OTU 44 0.04 0.15 0.02 0.04 0.06 0.12 0.07 0.14 0.748 0.908 0.660 0.858 0.452 0.715 0.052 0.155 OTU 39 0.02 0.07 0.01 0.02 0.07 0.20 0.08 0.19 0.769 0.927 0.726 0.893 0.253 0.475 0.046 0.147 OTU 29 0 0 0 0 0 0 0 0 0.002 0.017 OTU 2 10.86 14.76 24.38 24.19 0.13 0.26 0.31 1.13 0.046 0.147 0.817 0.946 0.001 0.011 0.001 0.011 OTU 38 1.51 5.31 0.17 0.67 0 0 0 0 0.145 0.326 0.002 0.017 OTU 42 0.51 1.20 0.01 0.03 0.67 1.71 0.01 0.03 0.012 0.057 0.041 0.136 0.717 0.890 0.669 0.864 OTU 17 0.46 1.30 0.02 0.05 2.79 7.57 0.05 0.15 0.041 0.136 0.063 0.176 0.243 0.466 0.571 0.770 OTU 1 14.87 24.08 5.33 7.93 22.17 26.59 13.03 17.69 0.069 0.190 0.231 0.452 0.295 0.526 0.062 0.176 OTU 11 0.69 1.32 0.51 0.97 2.63 7.62 3.10 5.11 0.362 0.623 0.692 0.875 0.458 0.719 0.003 0.020 OTU 4 0.51 2.00 0.17 0.56 1.34 4.60 2.14 7.58 0.571 0.770 0.611 0.806 0.525 0.770 0.147 0.326 OTU 48 0 0 0 0 0 0 0 0 0.036 0.131 OTU 14 0.24 0.69 0.22 0.43 3.77 8.30 4.66 10.97 0.542 0.770 0.747 0.908 0.023 0.091 0.004 0.025 OTU 46 0 0.02 0.01 0.02 0.26 0.65 0.25 0.50 0.348 0.609 0.991 1.000 0.028 0.106 0.039 0.134 OTU 31 0.23 0.55 0.05 0.12 0.87 1.67 0.33 0.51 0.137 0.326 0.170 0.368 0.166 0.364 0.016 0.068 OTU 45 0.05 0.09 0.01 0.01 0.35 0.56 1.02 1.62 0.023 0.091 0.096 0.250 0.016 0.068 0.004 0.025 OTU 10 0.37 1.03 0.20 0.46 4.39 11.22 4.97 10.40 0.477 0.736 0.824 0.946 0.013 0.059 0.003 0.020 OTU 32 0.12 0.43 0.23 0.79 0 0 0 0 0.540 0.770 0.868 0.975 0.012 0.057 0.006 0.034 OTU 8 0.28 1.29 0.03 0.10 1.43 5.01 2.34 7.10 0.537 0.770 0.551 0.770 0.370 0.624 0.138 0.326 OTU 6 1.17 3.54 0.13 0.28 9.20 15.81 1.39 1.56 0.238 0.461 0.007 0.039 0.021 0.087 0.001 0.011 OTU 36 0.03 0.11 0.11 0.22 0.68 1.66 0.25 0.49 0.144 0.326 0.263 0.488 0.003 0.020 0.220 0.445 OTU 35 0.57 1.28 0.02 0.04 0.90 2.13 0.02 0.08 0.012 0.057 0.034 0.126 0.542 0.770 0.867 0.975 OTU 7 1.07 2.73 1.41 2.66 3.52 7.28 6.47 12.19 0.832 0.946 0.282 0.518 0.125 0.320 0.037 0.132 OTU 16 0.73 3.50 0.27 1.01 1.41 3.77 1.96 4.92 0.905 0.990 0.562 0.770 0.400 0.656 0.146 0.326 OTU 27 0.98 2.31 0.02 0.07 1.56 4.02 0.01 0.05 0.012 0.057 0.048 0.151 0.563 0.770 0.719 0.890 OTU 20 1.68 4.52 0.05 0.18 0.86 4.28 0.91 4.07 0.049 0.151 0.981 0.997 0.448 0.715 0.997 1.000 OTU 50 0.09 0.15 0.84 0.95 0 0.01 0.06 0.23 0.001 0.011 0.486 0.737 0.001 0.011 0.002 0.017 OTU 22 0 0 0 0.02 0 0 0 0.01 0.231 0.452 0.882 0.985 OTU 47 0.12 0.53 0 0.02 0.32 1.55 0.06 0.22 0.191 0.395 0.917 0.990 0.933 0.990 0.180 0.381 OTU 41 0 0.01 0 0 0 0 0 0 0.228 0.452 1.000 1.000 OTU 23 0.12 0.50 0.01 0.02 0.07 0.20 0.09 0.23 0.136 0.326 0.682 0.874 0.819 0.946 0.024 0.093 OTU 43 0.01 0.03 0 0 0 0 0 0 OTU 34 0.03 0.14 0 0 0.06 0.16 0.14 0.38 0.903 0.990 0.417 0.672 0.390 0.645 0.051 0.155 OTU 24 0.11 0.52 0.18 0.39 1.18 1.89 1.10 1.90 0.567 0.770 0.973 0.997 0.001 0.011 0.003 0.020 a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. |
label | Table 2 |
caption | Relative abundances (%) of the most abundant OTUs in different gut sites of control birds (day 1–28). |
p | Relative abundances (%) of the most abundant OTUs in different gut sites of control birds (day 1–28). |
table | OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa OTU 49 0 0.02 0.05 0.11 0.01 0.02 0.01 0.02 0.056 0.164 0.655 0.858 0.366 0.623 0.133 0.326 OTU 25 1.89 4.01 0.06 0.07 1.05 2.95 0.01 0.02 0.001 0.011 0.015 0.067 0.365 0.623 0.001 0.011 OTU 5 12.41 25.84 13.09 21.85 0.28 0.56 0.07 0.09 0.920 0.990 0.039 0.134 0.002 0.017 0.001 0.011 OTU 30 0.45 1.45 0.40 0.72 0.74 1.11 1.25 2.09 0.913 0.990 0.385 0.643 0.808 0.946 0.059 0.170 OTU 9 0.90 2.72 1.03 3.05 3.56 9.78 5.82 15.04 0.938 0.990 0.514 0.765 0.196 0.401 0.091 0.244 OTU 13 1.34 5.22 0.75 1.84 1.36 4.51 1.41 4.43 0.714 0.890 0.831 0.946 0.940 0.990 0.549 0.770 OTU 15 0.07 0.20 0.13 0.32 1.17 1.98 4.21 9.38 0.792 0.942 0.095 0.250 0.005 0.030 0.001 0.011 OTU 18 2.36 8.46 2.34 6.03 0.08 0.23 0.03 0.09 0.961 0.994 0.409 0.665 0.081 0.220 0.013 0.059 OTU 21 0.65 2.01 0.32 0.87 0.53 1.11 1.08 3.21 0.588 0.787 0.599 0.796 0.812 0.946 0.294 0.526 OTU 33 0.96 1.38 2.57 5.92 0 0 0 0 0.341 0.603 0.001 0.011 OTU 12 0.95 2.20 1.25 4.71 2.42 5.21 5.41 11.82 0.776 0.929 0.285 0.519 0.491 0.739 0.131 0.326 OTU 28 3.21 7.19 2.99 7.77 0 0 0 0 0.941 0.990 0.006 0.034 0.001 0.011 0.001 0.011 OTU 37 0.12 0.56 0 0.01 0.39 1.93 0.07 0.28 0.140 0.326 0.939 0.990 0.947 0.991 0.177 0.379 OTU 40 0.05 0.11 1.08 1.53 0 0 0.10 0.44 0.001 0.011 0.464 0.722 0.001 0.011 0.008 0.043 OTU 3 10.36 20.66 18.43 23.28 0.39 0.63 1.52 5.30 0.252 0.475 0.517 0.765 0.001 0.011 0.002 0.017 OTU 26 0.03 0.07 0.03 0.06 1.34 2.35 1.75 3.25 0.483 0.737 0.691 0.875 0.001 0.011 0.003 0.020 OTU 19 0.80 1.99 0.22 0.57 1.09 2.22 1.01 2.17 0.189 0.395 0.979 0.997 0.961 0.994 0.134 0.326 OTU 44 0.04 0.15 0.02 0.04 0.06 0.12 0.07 0.14 0.748 0.908 0.660 0.858 0.452 0.715 0.052 0.155 OTU 39 0.02 0.07 0.01 0.02 0.07 0.20 0.08 0.19 0.769 0.927 0.726 0.893 0.253 0.475 0.046 0.147 OTU 29 0 0 0 0 0 0 0 0 0.002 0.017 OTU 2 10.86 14.76 24.38 24.19 0.13 0.26 0.31 1.13 0.046 0.147 0.817 0.946 0.001 0.011 0.001 0.011 OTU 38 1.51 5.31 0.17 0.67 0 0 0 0 0.145 0.326 0.002 0.017 OTU 42 0.51 1.20 0.01 0.03 0.67 1.71 0.01 0.03 0.012 0.057 0.041 0.136 0.717 0.890 0.669 0.864 OTU 17 0.46 1.30 0.02 0.05 2.79 7.57 0.05 0.15 0.041 0.136 0.063 0.176 0.243 0.466 0.571 0.770 OTU 1 14.87 24.08 5.33 7.93 22.17 26.59 13.03 17.69 0.069 0.190 0.231 0.452 0.295 0.526 0.062 0.176 OTU 11 0.69 1.32 0.51 0.97 2.63 7.62 3.10 5.11 0.362 0.623 0.692 0.875 0.458 0.719 0.003 0.020 OTU 4 0.51 2.00 0.17 0.56 1.34 4.60 2.14 7.58 0.571 0.770 0.611 0.806 0.525 0.770 0.147 0.326 OTU 48 0 0 0 0 0 0 0 0 0.036 0.131 OTU 14 0.24 0.69 0.22 0.43 3.77 8.30 4.66 10.97 0.542 0.770 0.747 0.908 0.023 0.091 0.004 0.025 OTU 46 0 0.02 0.01 0.02 0.26 0.65 0.25 0.50 0.348 0.609 0.991 1.000 0.028 0.106 0.039 0.134 OTU 31 0.23 0.55 0.05 0.12 0.87 1.67 0.33 0.51 0.137 0.326 0.170 0.368 0.166 0.364 0.016 0.068 OTU 45 0.05 0.09 0.01 0.01 0.35 0.56 1.02 1.62 0.023 0.091 0.096 0.250 0.016 0.068 0.004 0.025 OTU 10 0.37 1.03 0.20 0.46 4.39 11.22 4.97 10.40 0.477 0.736 0.824 0.946 0.013 0.059 0.003 0.020 OTU 32 0.12 0.43 0.23 0.79 0 0 0 0 0.540 0.770 0.868 0.975 0.012 0.057 0.006 0.034 OTU 8 0.28 1.29 0.03 0.10 1.43 5.01 2.34 7.10 0.537 0.770 0.551 0.770 0.370 0.624 0.138 0.326 OTU 6 1.17 3.54 0.13 0.28 9.20 15.81 1.39 1.56 0.238 0.461 0.007 0.039 0.021 0.087 0.001 0.011 OTU 36 0.03 0.11 0.11 0.22 0.68 1.66 0.25 0.49 0.144 0.326 0.263 0.488 0.003 0.020 0.220 0.445 OTU 35 0.57 1.28 0.02 0.04 0.90 2.13 0.02 0.08 0.012 0.057 0.034 0.126 0.542 0.770 0.867 0.975 OTU 7 1.07 2.73 1.41 2.66 3.52 7.28 6.47 12.19 0.832 0.946 0.282 0.518 0.125 0.320 0.037 0.132 OTU 16 0.73 3.50 0.27 1.01 1.41 3.77 1.96 4.92 0.905 0.990 0.562 0.770 0.400 0.656 0.146 0.326 OTU 27 0.98 2.31 0.02 0.07 1.56 4.02 0.01 0.05 0.012 0.057 0.048 0.151 0.563 0.770 0.719 0.890 OTU 20 1.68 4.52 0.05 0.18 0.86 4.28 0.91 4.07 0.049 0.151 0.981 0.997 0.448 0.715 0.997 1.000 OTU 50 0.09 0.15 0.84 0.95 0 0.01 0.06 0.23 0.001 0.011 0.486 0.737 0.001 0.011 0.002 0.017 OTU 22 0 0 0 0.02 0 0 0 0.01 0.231 0.452 0.882 0.985 OTU 47 0.12 0.53 0 0.02 0.32 1.55 0.06 0.22 0.191 0.395 0.917 0.990 0.933 0.990 0.180 0.381 OTU 41 0 0.01 0 0 0 0 0 0 0.228 0.452 1.000 1.000 OTU 23 0.12 0.50 0.01 0.02 0.07 0.20 0.09 0.23 0.136 0.326 0.682 0.874 0.819 0.946 0.024 0.093 OTU 43 0.01 0.03 0 0 0 0 0 0 OTU 34 0.03 0.14 0 0 0.06 0.16 0.14 0.38 0.903 0.990 0.417 0.672 0.390 0.645 0.051 0.155 OTU 24 0.11 0.52 0.18 0.39 1.18 1.89 1.10 1.90 0.567 0.770 0.973 0.997 0.001 0.011 0.003 0.020 |
tr | OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC |
th | OTUs ID |
th | Jejunum mucosa |
th | Jejunum content |
th | Cecum mucosa |
th | Cecum content |
th | JM-JC |
th | CM-CC |
th | JM-CM |
th | JC-CC |
tr | Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa |
th | Mean |
th | SD |
th | Mean |
th | SD |
th | Mean |
th | SD |
th | Mean |
th | SD |
th | P-values |
th | q-valuesa |
th | P-values |
th | q-valuesa |
th | P-values |
th | q-valuesa |
th | P-values |
th | q-valuesa |
tr | OTU 49 0 0.02 0.05 0.11 0.01 0.02 0.01 0.02 0.056 0.164 0.655 0.858 0.366 0.623 0.133 0.326 |
td | OTU 49 |
td | 0 |
td | 0.02 |
td | 0.05 |
td | 0.11 |
td | 0.01 |
td | 0.02 |
td | 0.01 |
td | 0.02 |
td | 0.056 |
td | 0.164 |
td | 0.655 |
td | 0.858 |
td | 0.366 |
td | 0.623 |
td | 0.133 |
td | 0.326 |
tr | OTU 25 1.89 4.01 0.06 0.07 1.05 2.95 0.01 0.02 0.001 0.011 0.015 0.067 0.365 0.623 0.001 0.011 |
td | OTU 25 |
td | 1.89 |
td | 4.01 |
td | 0.06 |
td | 0.07 |
td | 1.05 |
td | 2.95 |
td | 0.01 |
td | 0.02 |
td | 0.001 |
td | 0.011 |
td | 0.015 |
td | 0.067 |
td | 0.365 |
td | 0.623 |
td | 0.001 |
td | 0.011 |
tr | OTU 5 12.41 25.84 13.09 21.85 0.28 0.56 0.07 0.09 0.920 0.990 0.039 0.134 0.002 0.017 0.001 0.011 |
td | OTU 5 |
td | 12.41 |
td | 25.84 |
td | 13.09 |
td | 21.85 |
td | 0.28 |
td | 0.56 |
td | 0.07 |
td | 0.09 |
td | 0.920 |
td | 0.990 |
td | 0.039 |
td | 0.134 |
td | 0.002 |
td | 0.017 |
td | 0.001 |
td | 0.011 |
tr | OTU 30 0.45 1.45 0.40 0.72 0.74 1.11 1.25 2.09 0.913 0.990 0.385 0.643 0.808 0.946 0.059 0.170 |
td | OTU 30 |
td | 0.45 |
td | 1.45 |
td | 0.40 |
td | 0.72 |
td | 0.74 |
td | 1.11 |
td | 1.25 |
td | 2.09 |
td | 0.913 |
td | 0.990 |
td | 0.385 |
td | 0.643 |
td | 0.808 |
td | 0.946 |
td | 0.059 |
td | 0.170 |
tr | OTU 9 0.90 2.72 1.03 3.05 3.56 9.78 5.82 15.04 0.938 0.990 0.514 0.765 0.196 0.401 0.091 0.244 |
td | OTU 9 |
td | 0.90 |
td | 2.72 |
td | 1.03 |
td | 3.05 |
td | 3.56 |
td | 9.78 |
td | 5.82 |
td | 15.04 |
td | 0.938 |
td | 0.990 |
td | 0.514 |
td | 0.765 |
td | 0.196 |
td | 0.401 |
td | 0.091 |
td | 0.244 |
tr | OTU 13 1.34 5.22 0.75 1.84 1.36 4.51 1.41 4.43 0.714 0.890 0.831 0.946 0.940 0.990 0.549 0.770 |
td | OTU 13 |
td | 1.34 |
td | 5.22 |
td | 0.75 |
td | 1.84 |
td | 1.36 |
td | 4.51 |
td | 1.41 |
td | 4.43 |
td | 0.714 |
td | 0.890 |
td | 0.831 |
td | 0.946 |
td | 0.940 |
td | 0.990 |
td | 0.549 |
td | 0.770 |
tr | OTU 15 0.07 0.20 0.13 0.32 1.17 1.98 4.21 9.38 0.792 0.942 0.095 0.250 0.005 0.030 0.001 0.011 |
td | OTU 15 |
td | 0.07 |
td | 0.20 |
td | 0.13 |
td | 0.32 |
td | 1.17 |
td | 1.98 |
td | 4.21 |
td | 9.38 |
td | 0.792 |
td | 0.942 |
td | 0.095 |
td | 0.250 |
td | 0.005 |
td | 0.030 |
td | 0.001 |
td | 0.011 |
tr | OTU 18 2.36 8.46 2.34 6.03 0.08 0.23 0.03 0.09 0.961 0.994 0.409 0.665 0.081 0.220 0.013 0.059 |
td | OTU 18 |
td | 2.36 |
td | 8.46 |
td | 2.34 |
td | 6.03 |
td | 0.08 |
td | 0.23 |
td | 0.03 |
td | 0.09 |
td | 0.961 |
td | 0.994 |
td | 0.409 |
td | 0.665 |
td | 0.081 |
td | 0.220 |
td | 0.013 |
td | 0.059 |
tr | OTU 21 0.65 2.01 0.32 0.87 0.53 1.11 1.08 3.21 0.588 0.787 0.599 0.796 0.812 0.946 0.294 0.526 |
td | OTU 21 |
td | 0.65 |
td | 2.01 |
td | 0.32 |
td | 0.87 |
td | 0.53 |
td | 1.11 |
td | 1.08 |
td | 3.21 |
td | 0.588 |
td | 0.787 |
td | 0.599 |
td | 0.796 |
td | 0.812 |
td | 0.946 |
td | 0.294 |
td | 0.526 |
tr | OTU 33 0.96 1.38 2.57 5.92 0 0 0 0 0.341 0.603 0.001 0.011 |
td | OTU 33 |
td | 0.96 |
td | 1.38 |
td | 2.57 |
td | 5.92 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0.341 |
td | 0.603 |
td | 0.001 |
td | 0.011 |
tr | OTU 12 0.95 2.20 1.25 4.71 2.42 5.21 5.41 11.82 0.776 0.929 0.285 0.519 0.491 0.739 0.131 0.326 |
td | OTU 12 |
td | 0.95 |
td | 2.20 |
td | 1.25 |
td | 4.71 |
td | 2.42 |
td | 5.21 |
td | 5.41 |
td | 11.82 |
td | 0.776 |
td | 0.929 |
td | 0.285 |
td | 0.519 |
td | 0.491 |
td | 0.739 |
td | 0.131 |
td | 0.326 |
tr | OTU 28 3.21 7.19 2.99 7.77 0 0 0 0 0.941 0.990 0.006 0.034 0.001 0.011 0.001 0.011 |
td | OTU 28 |
td | 3.21 |
td | 7.19 |
td | 2.99 |
td | 7.77 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0.941 |
td | 0.990 |
td | 0.006 |
td | 0.034 |
td | 0.001 |
td | 0.011 |
td | 0.001 |
td | 0.011 |
tr | OTU 37 0.12 0.56 0 0.01 0.39 1.93 0.07 0.28 0.140 0.326 0.939 0.990 0.947 0.991 0.177 0.379 |
td | OTU 37 |
td | 0.12 |
td | 0.56 |
td | 0 |
td | 0.01 |
td | 0.39 |
td | 1.93 |
td | 0.07 |
td | 0.28 |
td | 0.140 |
td | 0.326 |
td | 0.939 |
td | 0.990 |
td | 0.947 |
td | 0.991 |
td | 0.177 |
td | 0.379 |
tr | OTU 40 0.05 0.11 1.08 1.53 0 0 0.10 0.44 0.001 0.011 0.464 0.722 0.001 0.011 0.008 0.043 |
td | OTU 40 |
td | 0.05 |
td | 0.11 |
td | 1.08 |
td | 1.53 |
td | 0 |
td | 0 |
td | 0.10 |
td | 0.44 |
td | 0.001 |
td | 0.011 |
td | 0.464 |
td | 0.722 |
td | 0.001 |
td | 0.011 |
td | 0.008 |
td | 0.043 |
tr | OTU 3 10.36 20.66 18.43 23.28 0.39 0.63 1.52 5.30 0.252 0.475 0.517 0.765 0.001 0.011 0.002 0.017 |
td | OTU 3 |
td | 10.36 |
td | 20.66 |
td | 18.43 |
td | 23.28 |
td | 0.39 |
td | 0.63 |
td | 1.52 |
td | 5.30 |
td | 0.252 |
td | 0.475 |
td | 0.517 |
td | 0.765 |
td | 0.001 |
td | 0.011 |
td | 0.002 |
td | 0.017 |
tr | OTU 26 0.03 0.07 0.03 0.06 1.34 2.35 1.75 3.25 0.483 0.737 0.691 0.875 0.001 0.011 0.003 0.020 |
td | OTU 26 |
td | 0.03 |
td | 0.07 |
td | 0.03 |
td | 0.06 |
td | 1.34 |
td | 2.35 |
td | 1.75 |
td | 3.25 |
td | 0.483 |
td | 0.737 |
td | 0.691 |
td | 0.875 |
td | 0.001 |
td | 0.011 |
td | 0.003 |
td | 0.020 |
tr | OTU 19 0.80 1.99 0.22 0.57 1.09 2.22 1.01 2.17 0.189 0.395 0.979 0.997 0.961 0.994 0.134 0.326 |
td | OTU 19 |
td | 0.80 |
td | 1.99 |
td | 0.22 |
td | 0.57 |
td | 1.09 |
td | 2.22 |
td | 1.01 |
td | 2.17 |
td | 0.189 |
td | 0.395 |
td | 0.979 |
td | 0.997 |
td | 0.961 |
td | 0.994 |
td | 0.134 |
td | 0.326 |
tr | OTU 44 0.04 0.15 0.02 0.04 0.06 0.12 0.07 0.14 0.748 0.908 0.660 0.858 0.452 0.715 0.052 0.155 |
td | OTU 44 |
td | 0.04 |
td | 0.15 |
td | 0.02 |
td | 0.04 |
td | 0.06 |
td | 0.12 |
td | 0.07 |
td | 0.14 |
td | 0.748 |
td | 0.908 |
td | 0.660 |
td | 0.858 |
td | 0.452 |
td | 0.715 |
td | 0.052 |
td | 0.155 |
tr | OTU 39 0.02 0.07 0.01 0.02 0.07 0.20 0.08 0.19 0.769 0.927 0.726 0.893 0.253 0.475 0.046 0.147 |
td | OTU 39 |
td | 0.02 |
td | 0.07 |
td | 0.01 |
td | 0.02 |
td | 0.07 |
td | 0.20 |
td | 0.08 |
td | 0.19 |
td | 0.769 |
td | 0.927 |
td | 0.726 |
td | 0.893 |
td | 0.253 |
td | 0.475 |
td | 0.046 |
td | 0.147 |
tr | OTU 29 0 0 0 0 0 0 0 0 0.002 0.017 |
td | OTU 29 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0.002 |
td | 0.017 |
tr | OTU 2 10.86 14.76 24.38 24.19 0.13 0.26 0.31 1.13 0.046 0.147 0.817 0.946 0.001 0.011 0.001 0.011 |
td | OTU 2 |
td | 10.86 |
td | 14.76 |
td | 24.38 |
td | 24.19 |
td | 0.13 |
td | 0.26 |
td | 0.31 |
td | 1.13 |
td | 0.046 |
td | 0.147 |
td | 0.817 |
td | 0.946 |
td | 0.001 |
td | 0.011 |
td | 0.001 |
td | 0.011 |
tr | OTU 38 1.51 5.31 0.17 0.67 0 0 0 0 0.145 0.326 0.002 0.017 |
td | OTU 38 |
td | 1.51 |
td | 5.31 |
td | 0.17 |
td | 0.67 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0.145 |
td | 0.326 |
td | 0.002 |
td | 0.017 |
tr | OTU 42 0.51 1.20 0.01 0.03 0.67 1.71 0.01 0.03 0.012 0.057 0.041 0.136 0.717 0.890 0.669 0.864 |
td | OTU 42 |
td | 0.51 |
td | 1.20 |
td | 0.01 |
td | 0.03 |
td | 0.67 |
td | 1.71 |
td | 0.01 |
td | 0.03 |
td | 0.012 |
td | 0.057 |
td | 0.041 |
td | 0.136 |
td | 0.717 |
td | 0.890 |
td | 0.669 |
td | 0.864 |
tr | OTU 17 0.46 1.30 0.02 0.05 2.79 7.57 0.05 0.15 0.041 0.136 0.063 0.176 0.243 0.466 0.571 0.770 |
td | OTU 17 |
td | 0.46 |
td | 1.30 |
td | 0.02 |
td | 0.05 |
td | 2.79 |
td | 7.57 |
td | 0.05 |
td | 0.15 |
td | 0.041 |
td | 0.136 |
td | 0.063 |
td | 0.176 |
td | 0.243 |
td | 0.466 |
td | 0.571 |
td | 0.770 |
tr | OTU 1 14.87 24.08 5.33 7.93 22.17 26.59 13.03 17.69 0.069 0.190 0.231 0.452 0.295 0.526 0.062 0.176 |
td | OTU 1 |
td | 14.87 |
td | 24.08 |
td | 5.33 |
td | 7.93 |
td | 22.17 |
td | 26.59 |
td | 13.03 |
td | 17.69 |
td | 0.069 |
td | 0.190 |
td | 0.231 |
td | 0.452 |
td | 0.295 |
td | 0.526 |
td | 0.062 |
td | 0.176 |
tr | OTU 11 0.69 1.32 0.51 0.97 2.63 7.62 3.10 5.11 0.362 0.623 0.692 0.875 0.458 0.719 0.003 0.020 |
td | OTU 11 |
td | 0.69 |
td | 1.32 |
td | 0.51 |
td | 0.97 |
td | 2.63 |
td | 7.62 |
td | 3.10 |
td | 5.11 |
td | 0.362 |
td | 0.623 |
td | 0.692 |
td | 0.875 |
td | 0.458 |
td | 0.719 |
td | 0.003 |
td | 0.020 |
tr | OTU 4 0.51 2.00 0.17 0.56 1.34 4.60 2.14 7.58 0.571 0.770 0.611 0.806 0.525 0.770 0.147 0.326 |
td | OTU 4 |
td | 0.51 |
td | 2.00 |
td | 0.17 |
td | 0.56 |
td | 1.34 |
td | 4.60 |
td | 2.14 |
td | 7.58 |
td | 0.571 |
td | 0.770 |
td | 0.611 |
td | 0.806 |
td | 0.525 |
td | 0.770 |
td | 0.147 |
td | 0.326 |
tr | OTU 48 0 0 0 0 0 0 0 0 0.036 0.131 |
td | OTU 48 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0.036 |
td | 0.131 |
tr | OTU 14 0.24 0.69 0.22 0.43 3.77 8.30 4.66 10.97 0.542 0.770 0.747 0.908 0.023 0.091 0.004 0.025 |
td | OTU 14 |
td | 0.24 |
td | 0.69 |
td | 0.22 |
td | 0.43 |
td | 3.77 |
td | 8.30 |
td | 4.66 |
td | 10.97 |
td | 0.542 |
td | 0.770 |
td | 0.747 |
td | 0.908 |
td | 0.023 |
td | 0.091 |
td | 0.004 |
td | 0.025 |
tr | OTU 46 0 0.02 0.01 0.02 0.26 0.65 0.25 0.50 0.348 0.609 0.991 1.000 0.028 0.106 0.039 0.134 |
td | OTU 46 |
td | 0 |
td | 0.02 |
td | 0.01 |
td | 0.02 |
td | 0.26 |
td | 0.65 |
td | 0.25 |
td | 0.50 |
td | 0.348 |
td | 0.609 |
td | 0.991 |
td | 1.000 |
td | 0.028 |
td | 0.106 |
td | 0.039 |
td | 0.134 |
tr | OTU 31 0.23 0.55 0.05 0.12 0.87 1.67 0.33 0.51 0.137 0.326 0.170 0.368 0.166 0.364 0.016 0.068 |
td | OTU 31 |
td | 0.23 |
td | 0.55 |
td | 0.05 |
td | 0.12 |
td | 0.87 |
td | 1.67 |
td | 0.33 |
td | 0.51 |
td | 0.137 |
td | 0.326 |
td | 0.170 |
td | 0.368 |
td | 0.166 |
td | 0.364 |
td | 0.016 |
td | 0.068 |
tr | OTU 45 0.05 0.09 0.01 0.01 0.35 0.56 1.02 1.62 0.023 0.091 0.096 0.250 0.016 0.068 0.004 0.025 |
td | OTU 45 |
td | 0.05 |
td | 0.09 |
td | 0.01 |
td | 0.01 |
td | 0.35 |
td | 0.56 |
td | 1.02 |
td | 1.62 |
td | 0.023 |
td | 0.091 |
td | 0.096 |
td | 0.250 |
td | 0.016 |
td | 0.068 |
td | 0.004 |
td | 0.025 |
tr | OTU 10 0.37 1.03 0.20 0.46 4.39 11.22 4.97 10.40 0.477 0.736 0.824 0.946 0.013 0.059 0.003 0.020 |
td | OTU 10 |
td | 0.37 |
td | 1.03 |
td | 0.20 |
td | 0.46 |
td | 4.39 |
td | 11.22 |
td | 4.97 |
td | 10.40 |
td | 0.477 |
td | 0.736 |
td | 0.824 |
td | 0.946 |
td | 0.013 |
td | 0.059 |
td | 0.003 |
td | 0.020 |
tr | OTU 32 0.12 0.43 0.23 0.79 0 0 0 0 0.540 0.770 0.868 0.975 0.012 0.057 0.006 0.034 |
td | OTU 32 |
td | 0.12 |
td | 0.43 |
td | 0.23 |
td | 0.79 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0.540 |
td | 0.770 |
td | 0.868 |
td | 0.975 |
td | 0.012 |
td | 0.057 |
td | 0.006 |
td | 0.034 |
tr | OTU 8 0.28 1.29 0.03 0.10 1.43 5.01 2.34 7.10 0.537 0.770 0.551 0.770 0.370 0.624 0.138 0.326 |
td | OTU 8 |
td | 0.28 |
td | 1.29 |
td | 0.03 |
td | 0.10 |
td | 1.43 |
td | 5.01 |
td | 2.34 |
td | 7.10 |
td | 0.537 |
td | 0.770 |
td | 0.551 |
td | 0.770 |
td | 0.370 |
td | 0.624 |
td | 0.138 |
td | 0.326 |
tr | OTU 6 1.17 3.54 0.13 0.28 9.20 15.81 1.39 1.56 0.238 0.461 0.007 0.039 0.021 0.087 0.001 0.011 |
td | OTU 6 |
td | 1.17 |
td | 3.54 |
td | 0.13 |
td | 0.28 |
td | 9.20 |
td | 15.81 |
td | 1.39 |
td | 1.56 |
td | 0.238 |
td | 0.461 |
td | 0.007 |
td | 0.039 |
td | 0.021 |
td | 0.087 |
td | 0.001 |
td | 0.011 |
tr | OTU 36 0.03 0.11 0.11 0.22 0.68 1.66 0.25 0.49 0.144 0.326 0.263 0.488 0.003 0.020 0.220 0.445 |
td | OTU 36 |
td | 0.03 |
td | 0.11 |
td | 0.11 |
td | 0.22 |
td | 0.68 |
td | 1.66 |
td | 0.25 |
td | 0.49 |
td | 0.144 |
td | 0.326 |
td | 0.263 |
td | 0.488 |
td | 0.003 |
td | 0.020 |
td | 0.220 |
td | 0.445 |
tr | OTU 35 0.57 1.28 0.02 0.04 0.90 2.13 0.02 0.08 0.012 0.057 0.034 0.126 0.542 0.770 0.867 0.975 |
td | OTU 35 |
td | 0.57 |
td | 1.28 |
td | 0.02 |
td | 0.04 |
td | 0.90 |
td | 2.13 |
td | 0.02 |
td | 0.08 |
td | 0.012 |
td | 0.057 |
td | 0.034 |
td | 0.126 |
td | 0.542 |
td | 0.770 |
td | 0.867 |
td | 0.975 |
tr | OTU 7 1.07 2.73 1.41 2.66 3.52 7.28 6.47 12.19 0.832 0.946 0.282 0.518 0.125 0.320 0.037 0.132 |
td | OTU 7 |
td | 1.07 |
td | 2.73 |
td | 1.41 |
td | 2.66 |
td | 3.52 |
td | 7.28 |
td | 6.47 |
td | 12.19 |
td | 0.832 |
td | 0.946 |
td | 0.282 |
td | 0.518 |
td | 0.125 |
td | 0.320 |
td | 0.037 |
td | 0.132 |
tr | OTU 16 0.73 3.50 0.27 1.01 1.41 3.77 1.96 4.92 0.905 0.990 0.562 0.770 0.400 0.656 0.146 0.326 |
td | OTU 16 |
td | 0.73 |
td | 3.50 |
td | 0.27 |
td | 1.01 |
td | 1.41 |
td | 3.77 |
td | 1.96 |
td | 4.92 |
td | 0.905 |
td | 0.990 |
td | 0.562 |
td | 0.770 |
td | 0.400 |
td | 0.656 |
td | 0.146 |
td | 0.326 |
tr | OTU 27 0.98 2.31 0.02 0.07 1.56 4.02 0.01 0.05 0.012 0.057 0.048 0.151 0.563 0.770 0.719 0.890 |
td | OTU 27 |
td | 0.98 |
td | 2.31 |
td | 0.02 |
td | 0.07 |
td | 1.56 |
td | 4.02 |
td | 0.01 |
td | 0.05 |
td | 0.012 |
td | 0.057 |
td | 0.048 |
td | 0.151 |
td | 0.563 |
td | 0.770 |
td | 0.719 |
td | 0.890 |
tr | OTU 20 1.68 4.52 0.05 0.18 0.86 4.28 0.91 4.07 0.049 0.151 0.981 0.997 0.448 0.715 0.997 1.000 |
td | OTU 20 |
td | 1.68 |
td | 4.52 |
td | 0.05 |
td | 0.18 |
td | 0.86 |
td | 4.28 |
td | 0.91 |
td | 4.07 |
td | 0.049 |
td | 0.151 |
td | 0.981 |
td | 0.997 |
td | 0.448 |
td | 0.715 |
td | 0.997 |
td | 1.000 |
tr | OTU 50 0.09 0.15 0.84 0.95 0 0.01 0.06 0.23 0.001 0.011 0.486 0.737 0.001 0.011 0.002 0.017 |
td | OTU 50 |
td | 0.09 |
td | 0.15 |
td | 0.84 |
td | 0.95 |
td | 0 |
td | 0.01 |
td | 0.06 |
td | 0.23 |
td | 0.001 |
td | 0.011 |
td | 0.486 |
td | 0.737 |
td | 0.001 |
td | 0.011 |
td | 0.002 |
td | 0.017 |
tr | OTU 22 0 0 0 0.02 0 0 0 0.01 0.231 0.452 0.882 0.985 |
td | OTU 22 |
td | 0 |
td | 0 |
td | 0 |
td | 0.02 |
td | 0 |
td | 0 |
td | 0 |
td | 0.01 |
td | 0.231 |
td | 0.452 |
td | 0.882 |
td | 0.985 |
tr | OTU 47 0.12 0.53 0 0.02 0.32 1.55 0.06 0.22 0.191 0.395 0.917 0.990 0.933 0.990 0.180 0.381 |
td | OTU 47 |
td | 0.12 |
td | 0.53 |
td | 0 |
td | 0.02 |
td | 0.32 |
td | 1.55 |
td | 0.06 |
td | 0.22 |
td | 0.191 |
td | 0.395 |
td | 0.917 |
td | 0.990 |
td | 0.933 |
td | 0.990 |
td | 0.180 |
td | 0.381 |
tr | OTU 41 0 0.01 0 0 0 0 0 0 0.228 0.452 1.000 1.000 |
td | OTU 41 |
td | 0 |
td | 0.01 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0.228 |
td | 0.452 |
td | 1.000 |
td | 1.000 |
tr | OTU 23 0.12 0.50 0.01 0.02 0.07 0.20 0.09 0.23 0.136 0.326 0.682 0.874 0.819 0.946 0.024 0.093 |
td | OTU 23 |
td | 0.12 |
td | 0.50 |
td | 0.01 |
td | 0.02 |
td | 0.07 |
td | 0.20 |
td | 0.09 |
td | 0.23 |
td | 0.136 |
td | 0.326 |
td | 0.682 |
td | 0.874 |
td | 0.819 |
td | 0.946 |
td | 0.024 |
td | 0.093 |
tr | OTU 43 0.01 0.03 0 0 0 0 0 0 |
td | OTU 43 |
td | 0.01 |
td | 0.03 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
tr | OTU 34 0.03 0.14 0 0 0.06 0.16 0.14 0.38 0.903 0.990 0.417 0.672 0.390 0.645 0.051 0.155 |
td | OTU 34 |
td | 0.03 |
td | 0.14 |
td | 0 |
td | 0 |
td | 0.06 |
td | 0.16 |
td | 0.14 |
td | 0.38 |
td | 0.903 |
td | 0.990 |
td | 0.417 |
td | 0.672 |
td | 0.390 |
td | 0.645 |
td | 0.051 |
td | 0.155 |
tr | OTU 24 0.11 0.52 0.18 0.39 1.18 1.89 1.10 1.90 0.567 0.770 0.973 0.997 0.001 0.011 0.003 0.020 |
td | OTU 24 |
td | 0.11 |
td | 0.52 |
td | 0.18 |
td | 0.39 |
td | 1.18 |
td | 1.89 |
td | 1.10 |
td | 1.90 |
td | 0.567 |
td | 0.770 |
td | 0.973 |
td | 0.997 |
td | 0.001 |
td | 0.011 |
td | 0.003 |
td | 0.020 |
table-wrap-foot | a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. |
footnote | a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. |
label | a |
p | q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. |
table-wrap | Table 3 Relative abundances (%) of the most abundant OTUs in different gut sites of infected birds (days 21 and 28). OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa OTU 49 0.18 0.28 0.43 0.98 0.61 1.44 0.52 0.91 0.689 0.880 0.936 0.989 0.550 0.791 0.516 0.776 OTU 25 0.02 0.04 0.08 0.09 0.00 0.00 0 0 0.077 0.178 0.063 0.168 OTU 5 1.65 2.21 8.89 6.18 0.01 0.01 0 0 0.009 0.043 0.761 0.927 0.001 0.007 0.001 0.007 OTU 30 0.31 0.94 0.06 0.08 0.30 0.38 0.16 0.12 0.957 0.989 0.355 0.596 1.000 1.000 0.013 0.056 OTU 9 0.17 0.39 0.14 0.14 1.47 4.29 2.06 5.88 0.903 0.987 0.575 0.791 0.530 0.785 0.217 0.408 OTU 13 0.64 1.06 0.72 1.35 2.87 3.77 2.65 2.58 0.955 0.989 0.950 0.989 0.056 0.159 0.020 0.071 OTU 15 0.08 0.13 0.01 0.02 1.24 0.89 2.13 1.23 0.049 0.146 0.040 0.126 0.001 0.007 0.001 0.007 OTU 18 4.67 9.39 6.34 11.77 0.19 0.44 0.14 0.36 0.572 0.791 0.857 0.986 0.102 0.218 0.011 0.051 OTU 21 0.28 0.58 0.16 0.19 1.63 2.60 1.93 2.41 0.565 0.791 0.611 0.611 0.085 0.191 0.009 0.043 OTU 33 1.11 1.14 0.13 0.13 0.00 0.00 0.00 0.00 0.008 0.041 1.000 1.000 0.001 0.007 0.001 0.007 OTU 12 0.51 0.74 0.06 0.08 0.06 0.09 0.05 0.05 0.056 0.159 0.929 0.989 0.062 0.168 0.796 0.949 OTU 28 1.19 1.20 0.20 0.21 0.00 0.00 0.00 0.00 0.015 0.060 0.016 0.060 0.001 0.007 0.001 0.007 OTU 37 0.14 0.27 0.01 0.02 0.35 0.18 0.51 0.27 0.074 0.178 0.077 0.178 0.207 0.394 0.001 0.007 OTU 40 0.07 0.08 1.35 0.83 0.01 0.01 0.00 0.01 0.001 0.007 0.881 0.987 0.008 0.041 0.001 0.007 OTU 3 11.02 13.33 29.61 19.69 0.52 0.56 0.41 0.45 0.067 0.173 0.865 0.986 0.004 0.023 0.001 0.007 OTU 26 0 0 0.01 0.05 0.01 0.01 0.01 0.01 0.542 0.791 0.801 0.949 0.070 0.176 0.990 1.000 OTU 19 0.14 0.29 0.31 0.24 3.24 7.48 2.09 5.77 0.372 0.613 0.614 0.823 0.107 0.223 0.441 0.700 OTU 44 0.43 1.20 0.07 0.12 0.49 0.94 1.06 2.17 0.594 0.809 0.574 0.791 0.552 0.791 0.014 0.059 OTU 39 0.02 0.05 0.13 0.20 0.59 0.79 1.02 1.34 0.072 0.178 0.318 0.539 0.001 0.007 0.016 0.060 OTU 29 0.30 0.66 0.01 0.03 3.92 6.25 0.38 0.51 0.052 0.152 0.049 0.146 0.036 0.115 0.005 0.028 OTU 2 19.98 22.32 23.46 10.10 0.85 1.46 0.19 0.30 0.834 0.975 0.285 0.493 0.002 0.012 0.001 0.007 OTU 38 0 0.01 0 0 0 0 0 0 0.690 0.012 OTU 42 0 0 0 0 0 0 0 0 OTU 17 0.62 1.33 0.25 0.31 4.45 6.58 0.12 0.18 0.451 0.703 0.002 0.012 0.091 0.201 0.531 0.785 OTU 1 0.11 0.18 0.81 1.36 0.28 0.40 0.19 0.36 0.145 0.292 0.760 0.927 0.280 0.491 0.255 0.455 OTU 11 1.09 1.39 0.10 0.10 2.01 2.44 2.31 3.56 0.026 0.086 0.761 0.927 0.907 0.987 0.007 0.038 OTU 4 3.43 6.60 0.13 0.11 12.51 8.03 16.82 10.92 0.154 0.303 0.162 0.315 0.016 0.060 0.001 0.007 OTU 48 0.41 1.14 0.01 0.02 2.29 7.23 0.38 1.17 0.225 0.414 0.747 0.927 0.817 0.962 0.222 0.413 OTU 14 0.24 0.65 0.07 0.07 0.45 0.84 1.41 2.08 0.364 0.606 0.122 0.251 0.619 0.824 0.076 0.178 OTU 46 0.21 0.60 0.01 0.02 0.49 0.81 0.52 0.87 0.306 0.524 0.757 0.927 0.396 0.646 0.016 0.060 OTU 31 0.03 0.06 0.03 0.04 0.37 0.52 0.08 0.07 0.955 0.989 0.057 0.159 0.012 0.055 0.019 0.068 OTU 45 0 0 0 0 0 0 0 0 1.000 1.000 0.281 0.491 OTU 10 0.26 0.82 0.09 0.12 0.29 0.57 0.22 0.30 0.960 0.989 0.896 0.987 0.891 0.987 0.175 0.336 OTU 32 2.90 3.72 3.80 3.98 0.18 0.46 0.05 0.11 0.872 0.986 0.567 0.791 0.004 0.023 0.001 0.007 OTU 8 1.21 2.88 0.05 0.09 7.75 7.99 6.25 8.70 0.036 0.115 0.917 0.989 0.021 0.073 0.001 0.007 OTU 6 0.82 1.99 0.10 0.13 4.11 2.46 1.24 1.97 0.455 0.703 0.026 0.086 0.019 0.068 0.001 0.007 OTU 36 0.21 0.40 0.23 0.21 0.34 0.37 0.19 0.22 0.893 0.987 0.441 0.700 0.473 0.724 0.871 0.986 OTU 35 0 0 0 0 0 0 0 0 OTU 7 0.24 0.40 0.08 0.17 4.65 13.62 6.23 18.65 0.095 0.205 0.692 0.880 0.501 0.760 0.062 0.168 OTU 16 0.19 0.27 0.29 0.47 1.37 1.80 1.55 1.94 0.776 0.932 0.653 0.862 0.074 0.178 0.048 0.146 OTU 27 0 0 0 0 0 0 0 0 OTU 20 0.22 0.67 0.03 0.05 4.32 13.62 0.62 1.88 0.849 0.986 0.770 0.932 0.576 0.791 0.424 0.686 OTU 50 0.10 0.17 1.20 0.73 0.01 0.01 0.01 0.01 0.001 0.007 0.979 1.000 0.013 0.056 0.001 0.007 OTU 22 0.14 0.42 0 0 2.08 5.32 3.60 9.82 0.107 0.223 0.671 0.877 0.236 0.430 0.001 0.007 OTU 47 0.03 0.06 0.01 0.01 0.20 0.10 0.31 0.23 0.244 0.440 0.092 0.201 0.001 0.007 0.001 0.007 OTU 41 0.99 2.99 0 0 0.50 0.87 1.28 3.32 0.723 0.913 0.923 0.989 OTU 23 0.63 1.18 0.02 0.02 2.39 2.31 2.88 2.65 0.124 0.252 0.448 0.703 0.064 0.168 0.001 0.007 OTU 43 8.90 28.14 0 0 0 0 0 0 OTU 34 0.02 0.05 0 0 0.85 0.79 1.54 1.09 0.148 0.294 0.068 0.173 0.001 0.007 0.001 0.007 OTU 24 0 0 0.05 0.07 0.15 0.13 0.12 0.11 0.674 0.877 0.082 0.187 a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. |
label | Table 3 |
caption | Relative abundances (%) of the most abundant OTUs in different gut sites of infected birds (days 21 and 28). |
p | Relative abundances (%) of the most abundant OTUs in different gut sites of infected birds (days 21 and 28). |
table | OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa OTU 49 0.18 0.28 0.43 0.98 0.61 1.44 0.52 0.91 0.689 0.880 0.936 0.989 0.550 0.791 0.516 0.776 OTU 25 0.02 0.04 0.08 0.09 0.00 0.00 0 0 0.077 0.178 0.063 0.168 OTU 5 1.65 2.21 8.89 6.18 0.01 0.01 0 0 0.009 0.043 0.761 0.927 0.001 0.007 0.001 0.007 OTU 30 0.31 0.94 0.06 0.08 0.30 0.38 0.16 0.12 0.957 0.989 0.355 0.596 1.000 1.000 0.013 0.056 OTU 9 0.17 0.39 0.14 0.14 1.47 4.29 2.06 5.88 0.903 0.987 0.575 0.791 0.530 0.785 0.217 0.408 OTU 13 0.64 1.06 0.72 1.35 2.87 3.77 2.65 2.58 0.955 0.989 0.950 0.989 0.056 0.159 0.020 0.071 OTU 15 0.08 0.13 0.01 0.02 1.24 0.89 2.13 1.23 0.049 0.146 0.040 0.126 0.001 0.007 0.001 0.007 OTU 18 4.67 9.39 6.34 11.77 0.19 0.44 0.14 0.36 0.572 0.791 0.857 0.986 0.102 0.218 0.011 0.051 OTU 21 0.28 0.58 0.16 0.19 1.63 2.60 1.93 2.41 0.565 0.791 0.611 0.611 0.085 0.191 0.009 0.043 OTU 33 1.11 1.14 0.13 0.13 0.00 0.00 0.00 0.00 0.008 0.041 1.000 1.000 0.001 0.007 0.001 0.007 OTU 12 0.51 0.74 0.06 0.08 0.06 0.09 0.05 0.05 0.056 0.159 0.929 0.989 0.062 0.168 0.796 0.949 OTU 28 1.19 1.20 0.20 0.21 0.00 0.00 0.00 0.00 0.015 0.060 0.016 0.060 0.001 0.007 0.001 0.007 OTU 37 0.14 0.27 0.01 0.02 0.35 0.18 0.51 0.27 0.074 0.178 0.077 0.178 0.207 0.394 0.001 0.007 OTU 40 0.07 0.08 1.35 0.83 0.01 0.01 0.00 0.01 0.001 0.007 0.881 0.987 0.008 0.041 0.001 0.007 OTU 3 11.02 13.33 29.61 19.69 0.52 0.56 0.41 0.45 0.067 0.173 0.865 0.986 0.004 0.023 0.001 0.007 OTU 26 0 0 0.01 0.05 0.01 0.01 0.01 0.01 0.542 0.791 0.801 0.949 0.070 0.176 0.990 1.000 OTU 19 0.14 0.29 0.31 0.24 3.24 7.48 2.09 5.77 0.372 0.613 0.614 0.823 0.107 0.223 0.441 0.700 OTU 44 0.43 1.20 0.07 0.12 0.49 0.94 1.06 2.17 0.594 0.809 0.574 0.791 0.552 0.791 0.014 0.059 OTU 39 0.02 0.05 0.13 0.20 0.59 0.79 1.02 1.34 0.072 0.178 0.318 0.539 0.001 0.007 0.016 0.060 OTU 29 0.30 0.66 0.01 0.03 3.92 6.25 0.38 0.51 0.052 0.152 0.049 0.146 0.036 0.115 0.005 0.028 OTU 2 19.98 22.32 23.46 10.10 0.85 1.46 0.19 0.30 0.834 0.975 0.285 0.493 0.002 0.012 0.001 0.007 OTU 38 0 0.01 0 0 0 0 0 0 0.690 0.012 OTU 42 0 0 0 0 0 0 0 0 OTU 17 0.62 1.33 0.25 0.31 4.45 6.58 0.12 0.18 0.451 0.703 0.002 0.012 0.091 0.201 0.531 0.785 OTU 1 0.11 0.18 0.81 1.36 0.28 0.40 0.19 0.36 0.145 0.292 0.760 0.927 0.280 0.491 0.255 0.455 OTU 11 1.09 1.39 0.10 0.10 2.01 2.44 2.31 3.56 0.026 0.086 0.761 0.927 0.907 0.987 0.007 0.038 OTU 4 3.43 6.60 0.13 0.11 12.51 8.03 16.82 10.92 0.154 0.303 0.162 0.315 0.016 0.060 0.001 0.007 OTU 48 0.41 1.14 0.01 0.02 2.29 7.23 0.38 1.17 0.225 0.414 0.747 0.927 0.817 0.962 0.222 0.413 OTU 14 0.24 0.65 0.07 0.07 0.45 0.84 1.41 2.08 0.364 0.606 0.122 0.251 0.619 0.824 0.076 0.178 OTU 46 0.21 0.60 0.01 0.02 0.49 0.81 0.52 0.87 0.306 0.524 0.757 0.927 0.396 0.646 0.016 0.060 OTU 31 0.03 0.06 0.03 0.04 0.37 0.52 0.08 0.07 0.955 0.989 0.057 0.159 0.012 0.055 0.019 0.068 OTU 45 0 0 0 0 0 0 0 0 1.000 1.000 0.281 0.491 OTU 10 0.26 0.82 0.09 0.12 0.29 0.57 0.22 0.30 0.960 0.989 0.896 0.987 0.891 0.987 0.175 0.336 OTU 32 2.90 3.72 3.80 3.98 0.18 0.46 0.05 0.11 0.872 0.986 0.567 0.791 0.004 0.023 0.001 0.007 OTU 8 1.21 2.88 0.05 0.09 7.75 7.99 6.25 8.70 0.036 0.115 0.917 0.989 0.021 0.073 0.001 0.007 OTU 6 0.82 1.99 0.10 0.13 4.11 2.46 1.24 1.97 0.455 0.703 0.026 0.086 0.019 0.068 0.001 0.007 OTU 36 0.21 0.40 0.23 0.21 0.34 0.37 0.19 0.22 0.893 0.987 0.441 0.700 0.473 0.724 0.871 0.986 OTU 35 0 0 0 0 0 0 0 0 OTU 7 0.24 0.40 0.08 0.17 4.65 13.62 6.23 18.65 0.095 0.205 0.692 0.880 0.501 0.760 0.062 0.168 OTU 16 0.19 0.27 0.29 0.47 1.37 1.80 1.55 1.94 0.776 0.932 0.653 0.862 0.074 0.178 0.048 0.146 OTU 27 0 0 0 0 0 0 0 0 OTU 20 0.22 0.67 0.03 0.05 4.32 13.62 0.62 1.88 0.849 0.986 0.770 0.932 0.576 0.791 0.424 0.686 OTU 50 0.10 0.17 1.20 0.73 0.01 0.01 0.01 0.01 0.001 0.007 0.979 1.000 0.013 0.056 0.001 0.007 OTU 22 0.14 0.42 0 0 2.08 5.32 3.60 9.82 0.107 0.223 0.671 0.877 0.236 0.430 0.001 0.007 OTU 47 0.03 0.06 0.01 0.01 0.20 0.10 0.31 0.23 0.244 0.440 0.092 0.201 0.001 0.007 0.001 0.007 OTU 41 0.99 2.99 0 0 0.50 0.87 1.28 3.32 0.723 0.913 0.923 0.989 OTU 23 0.63 1.18 0.02 0.02 2.39 2.31 2.88 2.65 0.124 0.252 0.448 0.703 0.064 0.168 0.001 0.007 OTU 43 8.90 28.14 0 0 0 0 0 0 OTU 34 0.02 0.05 0 0 0.85 0.79 1.54 1.09 0.148 0.294 0.068 0.173 0.001 0.007 0.001 0.007 OTU 24 0 0 0.05 0.07 0.15 0.13 0.12 0.11 0.674 0.877 0.082 0.187 |
tr | OTUs ID Jejunum mucosa Jejunum content Cecum mucosa Cecum content JM-JC CM-CC JM-CM JC-CC |
th | OTUs ID |
th | Jejunum mucosa |
th | Jejunum content |
th | Cecum mucosa |
th | Cecum content |
th | JM-JC |
th | CM-CC |
th | JM-CM |
th | JC-CC |
tr | Mean SD Mean SD Mean SD Mean SD P-values q-valuesa P-values q-valuesa P-values q-valuesa P-values q-valuesa |
th | Mean |
th | SD |
th | Mean |
th | SD |
th | Mean |
th | SD |
th | Mean |
th | SD |
th | P-values |
th | q-valuesa |
th | P-values |
th | q-valuesa |
th | P-values |
th | q-valuesa |
th | P-values |
th | q-valuesa |
tr | OTU 49 0.18 0.28 0.43 0.98 0.61 1.44 0.52 0.91 0.689 0.880 0.936 0.989 0.550 0.791 0.516 0.776 |
td | OTU 49 |
td | 0.18 |
td | 0.28 |
td | 0.43 |
td | 0.98 |
td | 0.61 |
td | 1.44 |
td | 0.52 |
td | 0.91 |
td | 0.689 |
td | 0.880 |
td | 0.936 |
td | 0.989 |
td | 0.550 |
td | 0.791 |
td | 0.516 |
td | 0.776 |
tr | OTU 25 0.02 0.04 0.08 0.09 0.00 0.00 0 0 0.077 0.178 0.063 0.168 |
td | OTU 25 |
td | 0.02 |
td | 0.04 |
td | 0.08 |
td | 0.09 |
td | 0.00 |
td | 0.00 |
td | 0 |
td | 0 |
td | 0.077 |
td | 0.178 |
td | 0.063 |
td | 0.168 |
tr | OTU 5 1.65 2.21 8.89 6.18 0.01 0.01 0 0 0.009 0.043 0.761 0.927 0.001 0.007 0.001 0.007 |
td | OTU 5 |
td | 1.65 |
td | 2.21 |
td | 8.89 |
td | 6.18 |
td | 0.01 |
td | 0.01 |
td | 0 |
td | 0 |
td | 0.009 |
td | 0.043 |
td | 0.761 |
td | 0.927 |
td | 0.001 |
td | 0.007 |
td | 0.001 |
td | 0.007 |
tr | OTU 30 0.31 0.94 0.06 0.08 0.30 0.38 0.16 0.12 0.957 0.989 0.355 0.596 1.000 1.000 0.013 0.056 |
td | OTU 30 |
td | 0.31 |
td | 0.94 |
td | 0.06 |
td | 0.08 |
td | 0.30 |
td | 0.38 |
td | 0.16 |
td | 0.12 |
td | 0.957 |
td | 0.989 |
td | 0.355 |
td | 0.596 |
td | 1.000 |
td | 1.000 |
td | 0.013 |
td | 0.056 |
tr | OTU 9 0.17 0.39 0.14 0.14 1.47 4.29 2.06 5.88 0.903 0.987 0.575 0.791 0.530 0.785 0.217 0.408 |
td | OTU 9 |
td | 0.17 |
td | 0.39 |
td | 0.14 |
td | 0.14 |
td | 1.47 |
td | 4.29 |
td | 2.06 |
td | 5.88 |
td | 0.903 |
td | 0.987 |
td | 0.575 |
td | 0.791 |
td | 0.530 |
td | 0.785 |
td | 0.217 |
td | 0.408 |
tr | OTU 13 0.64 1.06 0.72 1.35 2.87 3.77 2.65 2.58 0.955 0.989 0.950 0.989 0.056 0.159 0.020 0.071 |
td | OTU 13 |
td | 0.64 |
td | 1.06 |
td | 0.72 |
td | 1.35 |
td | 2.87 |
td | 3.77 |
td | 2.65 |
td | 2.58 |
td | 0.955 |
td | 0.989 |
td | 0.950 |
td | 0.989 |
td | 0.056 |
td | 0.159 |
td | 0.020 |
td | 0.071 |
tr | OTU 15 0.08 0.13 0.01 0.02 1.24 0.89 2.13 1.23 0.049 0.146 0.040 0.126 0.001 0.007 0.001 0.007 |
td | OTU 15 |
td | 0.08 |
td | 0.13 |
td | 0.01 |
td | 0.02 |
td | 1.24 |
td | 0.89 |
td | 2.13 |
td | 1.23 |
td | 0.049 |
td | 0.146 |
td | 0.040 |
td | 0.126 |
td | 0.001 |
td | 0.007 |
td | 0.001 |
td | 0.007 |
tr | OTU 18 4.67 9.39 6.34 11.77 0.19 0.44 0.14 0.36 0.572 0.791 0.857 0.986 0.102 0.218 0.011 0.051 |
td | OTU 18 |
td | 4.67 |
td | 9.39 |
td | 6.34 |
td | 11.77 |
td | 0.19 |
td | 0.44 |
td | 0.14 |
td | 0.36 |
td | 0.572 |
td | 0.791 |
td | 0.857 |
td | 0.986 |
td | 0.102 |
td | 0.218 |
td | 0.011 |
td | 0.051 |
tr | OTU 21 0.28 0.58 0.16 0.19 1.63 2.60 1.93 2.41 0.565 0.791 0.611 0.611 0.085 0.191 0.009 0.043 |
td | OTU 21 |
td | 0.28 |
td | 0.58 |
td | 0.16 |
td | 0.19 |
td | 1.63 |
td | 2.60 |
td | 1.93 |
td | 2.41 |
td | 0.565 |
td | 0.791 |
td | 0.611 |
td | 0.611 |
td | 0.085 |
td | 0.191 |
td | 0.009 |
td | 0.043 |
tr | OTU 33 1.11 1.14 0.13 0.13 0.00 0.00 0.00 0.00 0.008 0.041 1.000 1.000 0.001 0.007 0.001 0.007 |
td | OTU 33 |
td | 1.11 |
td | 1.14 |
td | 0.13 |
td | 0.13 |
td | 0.00 |
td | 0.00 |
td | 0.00 |
td | 0.00 |
td | 0.008 |
td | 0.041 |
td | 1.000 |
td | 1.000 |
td | 0.001 |
td | 0.007 |
td | 0.001 |
td | 0.007 |
tr | OTU 12 0.51 0.74 0.06 0.08 0.06 0.09 0.05 0.05 0.056 0.159 0.929 0.989 0.062 0.168 0.796 0.949 |
td | OTU 12 |
td | 0.51 |
td | 0.74 |
td | 0.06 |
td | 0.08 |
td | 0.06 |
td | 0.09 |
td | 0.05 |
td | 0.05 |
td | 0.056 |
td | 0.159 |
td | 0.929 |
td | 0.989 |
td | 0.062 |
td | 0.168 |
td | 0.796 |
td | 0.949 |
tr | OTU 28 1.19 1.20 0.20 0.21 0.00 0.00 0.00 0.00 0.015 0.060 0.016 0.060 0.001 0.007 0.001 0.007 |
td | OTU 28 |
td | 1.19 |
td | 1.20 |
td | 0.20 |
td | 0.21 |
td | 0.00 |
td | 0.00 |
td | 0.00 |
td | 0.00 |
td | 0.015 |
td | 0.060 |
td | 0.016 |
td | 0.060 |
td | 0.001 |
td | 0.007 |
td | 0.001 |
td | 0.007 |
tr | OTU 37 0.14 0.27 0.01 0.02 0.35 0.18 0.51 0.27 0.074 0.178 0.077 0.178 0.207 0.394 0.001 0.007 |
td | OTU 37 |
td | 0.14 |
td | 0.27 |
td | 0.01 |
td | 0.02 |
td | 0.35 |
td | 0.18 |
td | 0.51 |
td | 0.27 |
td | 0.074 |
td | 0.178 |
td | 0.077 |
td | 0.178 |
td | 0.207 |
td | 0.394 |
td | 0.001 |
td | 0.007 |
tr | OTU 40 0.07 0.08 1.35 0.83 0.01 0.01 0.00 0.01 0.001 0.007 0.881 0.987 0.008 0.041 0.001 0.007 |
td | OTU 40 |
td | 0.07 |
td | 0.08 |
td | 1.35 |
td | 0.83 |
td | 0.01 |
td | 0.01 |
td | 0.00 |
td | 0.01 |
td | 0.001 |
td | 0.007 |
td | 0.881 |
td | 0.987 |
td | 0.008 |
td | 0.041 |
td | 0.001 |
td | 0.007 |
tr | OTU 3 11.02 13.33 29.61 19.69 0.52 0.56 0.41 0.45 0.067 0.173 0.865 0.986 0.004 0.023 0.001 0.007 |
td | OTU 3 |
td | 11.02 |
td | 13.33 |
td | 29.61 |
td | 19.69 |
td | 0.52 |
td | 0.56 |
td | 0.41 |
td | 0.45 |
td | 0.067 |
td | 0.173 |
td | 0.865 |
td | 0.986 |
td | 0.004 |
td | 0.023 |
td | 0.001 |
td | 0.007 |
tr | OTU 26 0 0 0.01 0.05 0.01 0.01 0.01 0.01 0.542 0.791 0.801 0.949 0.070 0.176 0.990 1.000 |
td | OTU 26 |
td | 0 |
td | 0 |
td | 0.01 |
td | 0.05 |
td | 0.01 |
td | 0.01 |
td | 0.01 |
td | 0.01 |
td | 0.542 |
td | 0.791 |
td | 0.801 |
td | 0.949 |
td | 0.070 |
td | 0.176 |
td | 0.990 |
td | 1.000 |
tr | OTU 19 0.14 0.29 0.31 0.24 3.24 7.48 2.09 5.77 0.372 0.613 0.614 0.823 0.107 0.223 0.441 0.700 |
td | OTU 19 |
td | 0.14 |
td | 0.29 |
td | 0.31 |
td | 0.24 |
td | 3.24 |
td | 7.48 |
td | 2.09 |
td | 5.77 |
td | 0.372 |
td | 0.613 |
td | 0.614 |
td | 0.823 |
td | 0.107 |
td | 0.223 |
td | 0.441 |
td | 0.700 |
tr | OTU 44 0.43 1.20 0.07 0.12 0.49 0.94 1.06 2.17 0.594 0.809 0.574 0.791 0.552 0.791 0.014 0.059 |
td | OTU 44 |
td | 0.43 |
td | 1.20 |
td | 0.07 |
td | 0.12 |
td | 0.49 |
td | 0.94 |
td | 1.06 |
td | 2.17 |
td | 0.594 |
td | 0.809 |
td | 0.574 |
td | 0.791 |
td | 0.552 |
td | 0.791 |
td | 0.014 |
td | 0.059 |
tr | OTU 39 0.02 0.05 0.13 0.20 0.59 0.79 1.02 1.34 0.072 0.178 0.318 0.539 0.001 0.007 0.016 0.060 |
td | OTU 39 |
td | 0.02 |
td | 0.05 |
td | 0.13 |
td | 0.20 |
td | 0.59 |
td | 0.79 |
td | 1.02 |
td | 1.34 |
td | 0.072 |
td | 0.178 |
td | 0.318 |
td | 0.539 |
td | 0.001 |
td | 0.007 |
td | 0.016 |
td | 0.060 |
tr | OTU 29 0.30 0.66 0.01 0.03 3.92 6.25 0.38 0.51 0.052 0.152 0.049 0.146 0.036 0.115 0.005 0.028 |
td | OTU 29 |
td | 0.30 |
td | 0.66 |
td | 0.01 |
td | 0.03 |
td | 3.92 |
td | 6.25 |
td | 0.38 |
td | 0.51 |
td | 0.052 |
td | 0.152 |
td | 0.049 |
td | 0.146 |
td | 0.036 |
td | 0.115 |
td | 0.005 |
td | 0.028 |
tr | OTU 2 19.98 22.32 23.46 10.10 0.85 1.46 0.19 0.30 0.834 0.975 0.285 0.493 0.002 0.012 0.001 0.007 |
td | OTU 2 |
td | 19.98 |
td | 22.32 |
td | 23.46 |
td | 10.10 |
td | 0.85 |
td | 1.46 |
td | 0.19 |
td | 0.30 |
td | 0.834 |
td | 0.975 |
td | 0.285 |
td | 0.493 |
td | 0.002 |
td | 0.012 |
td | 0.001 |
td | 0.007 |
tr | OTU 38 0 0.01 0 0 0 0 0 0 0.690 0.012 |
td | OTU 38 |
td | 0 |
td | 0.01 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0.690 |
td | 0.012 |
tr | OTU 42 0 0 0 0 0 0 0 0 |
td | OTU 42 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
tr | OTU 17 0.62 1.33 0.25 0.31 4.45 6.58 0.12 0.18 0.451 0.703 0.002 0.012 0.091 0.201 0.531 0.785 |
td | OTU 17 |
td | 0.62 |
td | 1.33 |
td | 0.25 |
td | 0.31 |
td | 4.45 |
td | 6.58 |
td | 0.12 |
td | 0.18 |
td | 0.451 |
td | 0.703 |
td | 0.002 |
td | 0.012 |
td | 0.091 |
td | 0.201 |
td | 0.531 |
td | 0.785 |
tr | OTU 1 0.11 0.18 0.81 1.36 0.28 0.40 0.19 0.36 0.145 0.292 0.760 0.927 0.280 0.491 0.255 0.455 |
td | OTU 1 |
td | 0.11 |
td | 0.18 |
td | 0.81 |
td | 1.36 |
td | 0.28 |
td | 0.40 |
td | 0.19 |
td | 0.36 |
td | 0.145 |
td | 0.292 |
td | 0.760 |
td | 0.927 |
td | 0.280 |
td | 0.491 |
td | 0.255 |
td | 0.455 |
tr | OTU 11 1.09 1.39 0.10 0.10 2.01 2.44 2.31 3.56 0.026 0.086 0.761 0.927 0.907 0.987 0.007 0.038 |
td | OTU 11 |
td | 1.09 |
td | 1.39 |
td | 0.10 |
td | 0.10 |
td | 2.01 |
td | 2.44 |
td | 2.31 |
td | 3.56 |
td | 0.026 |
td | 0.086 |
td | 0.761 |
td | 0.927 |
td | 0.907 |
td | 0.987 |
td | 0.007 |
td | 0.038 |
tr | OTU 4 3.43 6.60 0.13 0.11 12.51 8.03 16.82 10.92 0.154 0.303 0.162 0.315 0.016 0.060 0.001 0.007 |
td | OTU 4 |
td | 3.43 |
td | 6.60 |
td | 0.13 |
td | 0.11 |
td | 12.51 |
td | 8.03 |
td | 16.82 |
td | 10.92 |
td | 0.154 |
td | 0.303 |
td | 0.162 |
td | 0.315 |
td | 0.016 |
td | 0.060 |
td | 0.001 |
td | 0.007 |
tr | OTU 48 0.41 1.14 0.01 0.02 2.29 7.23 0.38 1.17 0.225 0.414 0.747 0.927 0.817 0.962 0.222 0.413 |
td | OTU 48 |
td | 0.41 |
td | 1.14 |
td | 0.01 |
td | 0.02 |
td | 2.29 |
td | 7.23 |
td | 0.38 |
td | 1.17 |
td | 0.225 |
td | 0.414 |
td | 0.747 |
td | 0.927 |
td | 0.817 |
td | 0.962 |
td | 0.222 |
td | 0.413 |
tr | OTU 14 0.24 0.65 0.07 0.07 0.45 0.84 1.41 2.08 0.364 0.606 0.122 0.251 0.619 0.824 0.076 0.178 |
td | OTU 14 |
td | 0.24 |
td | 0.65 |
td | 0.07 |
td | 0.07 |
td | 0.45 |
td | 0.84 |
td | 1.41 |
td | 2.08 |
td | 0.364 |
td | 0.606 |
td | 0.122 |
td | 0.251 |
td | 0.619 |
td | 0.824 |
td | 0.076 |
td | 0.178 |
tr | OTU 46 0.21 0.60 0.01 0.02 0.49 0.81 0.52 0.87 0.306 0.524 0.757 0.927 0.396 0.646 0.016 0.060 |
td | OTU 46 |
td | 0.21 |
td | 0.60 |
td | 0.01 |
td | 0.02 |
td | 0.49 |
td | 0.81 |
td | 0.52 |
td | 0.87 |
td | 0.306 |
td | 0.524 |
td | 0.757 |
td | 0.927 |
td | 0.396 |
td | 0.646 |
td | 0.016 |
td | 0.060 |
tr | OTU 31 0.03 0.06 0.03 0.04 0.37 0.52 0.08 0.07 0.955 0.989 0.057 0.159 0.012 0.055 0.019 0.068 |
td | OTU 31 |
td | 0.03 |
td | 0.06 |
td | 0.03 |
td | 0.04 |
td | 0.37 |
td | 0.52 |
td | 0.08 |
td | 0.07 |
td | 0.955 |
td | 0.989 |
td | 0.057 |
td | 0.159 |
td | 0.012 |
td | 0.055 |
td | 0.019 |
td | 0.068 |
tr | OTU 45 0 0 0 0 0 0 0 0 1.000 1.000 0.281 0.491 |
td | OTU 45 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 1.000 |
td | 1.000 |
td | 0.281 |
td | 0.491 |
tr | OTU 10 0.26 0.82 0.09 0.12 0.29 0.57 0.22 0.30 0.960 0.989 0.896 0.987 0.891 0.987 0.175 0.336 |
td | OTU 10 |
td | 0.26 |
td | 0.82 |
td | 0.09 |
td | 0.12 |
td | 0.29 |
td | 0.57 |
td | 0.22 |
td | 0.30 |
td | 0.960 |
td | 0.989 |
td | 0.896 |
td | 0.987 |
td | 0.891 |
td | 0.987 |
td | 0.175 |
td | 0.336 |
tr | OTU 32 2.90 3.72 3.80 3.98 0.18 0.46 0.05 0.11 0.872 0.986 0.567 0.791 0.004 0.023 0.001 0.007 |
td | OTU 32 |
td | 2.90 |
td | 3.72 |
td | 3.80 |
td | 3.98 |
td | 0.18 |
td | 0.46 |
td | 0.05 |
td | 0.11 |
td | 0.872 |
td | 0.986 |
td | 0.567 |
td | 0.791 |
td | 0.004 |
td | 0.023 |
td | 0.001 |
td | 0.007 |
tr | OTU 8 1.21 2.88 0.05 0.09 7.75 7.99 6.25 8.70 0.036 0.115 0.917 0.989 0.021 0.073 0.001 0.007 |
td | OTU 8 |
td | 1.21 |
td | 2.88 |
td | 0.05 |
td | 0.09 |
td | 7.75 |
td | 7.99 |
td | 6.25 |
td | 8.70 |
td | 0.036 |
td | 0.115 |
td | 0.917 |
td | 0.989 |
td | 0.021 |
td | 0.073 |
td | 0.001 |
td | 0.007 |
tr | OTU 6 0.82 1.99 0.10 0.13 4.11 2.46 1.24 1.97 0.455 0.703 0.026 0.086 0.019 0.068 0.001 0.007 |
td | OTU 6 |
td | 0.82 |
td | 1.99 |
td | 0.10 |
td | 0.13 |
td | 4.11 |
td | 2.46 |
td | 1.24 |
td | 1.97 |
td | 0.455 |
td | 0.703 |
td | 0.026 |
td | 0.086 |
td | 0.019 |
td | 0.068 |
td | 0.001 |
td | 0.007 |
tr | OTU 36 0.21 0.40 0.23 0.21 0.34 0.37 0.19 0.22 0.893 0.987 0.441 0.700 0.473 0.724 0.871 0.986 |
td | OTU 36 |
td | 0.21 |
td | 0.40 |
td | 0.23 |
td | 0.21 |
td | 0.34 |
td | 0.37 |
td | 0.19 |
td | 0.22 |
td | 0.893 |
td | 0.987 |
td | 0.441 |
td | 0.700 |
td | 0.473 |
td | 0.724 |
td | 0.871 |
td | 0.986 |
tr | OTU 35 0 0 0 0 0 0 0 0 |
td | OTU 35 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
tr | OTU 7 0.24 0.40 0.08 0.17 4.65 13.62 6.23 18.65 0.095 0.205 0.692 0.880 0.501 0.760 0.062 0.168 |
td | OTU 7 |
td | 0.24 |
td | 0.40 |
td | 0.08 |
td | 0.17 |
td | 4.65 |
td | 13.62 |
td | 6.23 |
td | 18.65 |
td | 0.095 |
td | 0.205 |
td | 0.692 |
td | 0.880 |
td | 0.501 |
td | 0.760 |
td | 0.062 |
td | 0.168 |
tr | OTU 16 0.19 0.27 0.29 0.47 1.37 1.80 1.55 1.94 0.776 0.932 0.653 0.862 0.074 0.178 0.048 0.146 |
td | OTU 16 |
td | 0.19 |
td | 0.27 |
td | 0.29 |
td | 0.47 |
td | 1.37 |
td | 1.80 |
td | 1.55 |
td | 1.94 |
td | 0.776 |
td | 0.932 |
td | 0.653 |
td | 0.862 |
td | 0.074 |
td | 0.178 |
td | 0.048 |
td | 0.146 |
tr | OTU 27 0 0 0 0 0 0 0 0 |
td | OTU 27 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
tr | OTU 20 0.22 0.67 0.03 0.05 4.32 13.62 0.62 1.88 0.849 0.986 0.770 0.932 0.576 0.791 0.424 0.686 |
td | OTU 20 |
td | 0.22 |
td | 0.67 |
td | 0.03 |
td | 0.05 |
td | 4.32 |
td | 13.62 |
td | 0.62 |
td | 1.88 |
td | 0.849 |
td | 0.986 |
td | 0.770 |
td | 0.932 |
td | 0.576 |
td | 0.791 |
td | 0.424 |
td | 0.686 |
tr | OTU 50 0.10 0.17 1.20 0.73 0.01 0.01 0.01 0.01 0.001 0.007 0.979 1.000 0.013 0.056 0.001 0.007 |
td | OTU 50 |
td | 0.10 |
td | 0.17 |
td | 1.20 |
td | 0.73 |
td | 0.01 |
td | 0.01 |
td | 0.01 |
td | 0.01 |
td | 0.001 |
td | 0.007 |
td | 0.979 |
td | 1.000 |
td | 0.013 |
td | 0.056 |
td | 0.001 |
td | 0.007 |
tr | OTU 22 0.14 0.42 0 0 2.08 5.32 3.60 9.82 0.107 0.223 0.671 0.877 0.236 0.430 0.001 0.007 |
td | OTU 22 |
td | 0.14 |
td | 0.42 |
td | 0 |
td | 0 |
td | 2.08 |
td | 5.32 |
td | 3.60 |
td | 9.82 |
td | 0.107 |
td | 0.223 |
td | 0.671 |
td | 0.877 |
td | 0.236 |
td | 0.430 |
td | 0.001 |
td | 0.007 |
tr | OTU 47 0.03 0.06 0.01 0.01 0.20 0.10 0.31 0.23 0.244 0.440 0.092 0.201 0.001 0.007 0.001 0.007 |
td | OTU 47 |
td | 0.03 |
td | 0.06 |
td | 0.01 |
td | 0.01 |
td | 0.20 |
td | 0.10 |
td | 0.31 |
td | 0.23 |
td | 0.244 |
td | 0.440 |
td | 0.092 |
td | 0.201 |
td | 0.001 |
td | 0.007 |
td | 0.001 |
td | 0.007 |
tr | OTU 41 0.99 2.99 0 0 0.50 0.87 1.28 3.32 0.723 0.913 0.923 0.989 |
td | OTU 41 |
td | 0.99 |
td | 2.99 |
td | 0 |
td | 0 |
td | 0.50 |
td | 0.87 |
td | 1.28 |
td | 3.32 |
td | 0.723 |
td | 0.913 |
td | 0.923 |
td | 0.989 |
tr | OTU 23 0.63 1.18 0.02 0.02 2.39 2.31 2.88 2.65 0.124 0.252 0.448 0.703 0.064 0.168 0.001 0.007 |
td | OTU 23 |
td | 0.63 |
td | 1.18 |
td | 0.02 |
td | 0.02 |
td | 2.39 |
td | 2.31 |
td | 2.88 |
td | 2.65 |
td | 0.124 |
td | 0.252 |
td | 0.448 |
td | 0.703 |
td | 0.064 |
td | 0.168 |
td | 0.001 |
td | 0.007 |
tr | OTU 43 8.90 28.14 0 0 0 0 0 0 |
td | OTU 43 |
td | 8.90 |
td | 28.14 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
td | 0 |
tr | OTU 34 0.02 0.05 0 0 0.85 0.79 1.54 1.09 0.148 0.294 0.068 0.173 0.001 0.007 0.001 0.007 |
td | OTU 34 |
td | 0.02 |
td | 0.05 |
td | 0 |
td | 0 |
td | 0.85 |
td | 0.79 |
td | 1.54 |
td | 1.09 |
td | 0.148 |
td | 0.294 |
td | 0.068 |
td | 0.173 |
td | 0.001 |
td | 0.007 |
td | 0.001 |
td | 0.007 |
tr | OTU 24 0 0 0.05 0.07 0.15 0.13 0.12 0.11 0.674 0.877 0.082 0.187 |
td | OTU 24 |
td | 0 |
td | 0 |
td | 0.05 |
td | 0.07 |
td | 0.15 |
td | 0.13 |
td | 0.12 |
td | 0.11 |
td | 0.674 |
td | 0.877 |
td | 0.082 |
td | 0.187 |
table-wrap-foot | a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. |
footnote | a q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. |
label | a |
p | q-value: The False Discovery Rate (FDR) adjusted p-value using Benjamini and Hochberg method and the q < 0.25 after FDR correction considered significant. Statistically significant values are formatted in bold. |
p | The OTUs and species abundances sorted by gut sites of the infected birds compared with the control birds are shown in the heatmaps (Figure 2). Interestingly, in the infected birds, the abundance of E. coli and Eubacterium desmolans (best type strain hits) were lower at different gut sites (Figure 3A). On the contrary, Clostridium spp. abundance was higher in the infected birds compared with the negative controls (Figure 3B). |
figure | Figure 2 Heatmap showing the relative abundances (%) of the 50 most-abundant OTUs sorted by gut sites of the infected birds compared with the controls at the two sampling points post infection. The heat map integrates relative abundance of a given phylotype. Colour scaling is ranged from 0 to ≥ 25%. n.d, not detected. |
label | Figure 2 |
caption | Heatmap showing the relative abundances (%) of the 50 most-abundant OTUs sorted by gut sites of the infected birds compared with the controls at the two sampling points post infection. The heat map integrates relative abundance of a given phylotype. Colour scaling is ranged from 0 to ≥ 25%. n.d, not detected. |
p | Heatmap showing the relative abundances (%) of the 50 most-abundant OTUs sorted by gut sites of the infected birds compared with the controls at the two sampling points post infection. The heat map integrates relative abundance of a given phylotype. Colour scaling is ranged from 0 to ≥ 25%. n.d, not detected. |
figure | Figure 3 Relative abundances (%) of the most relevant OTUs in the infected birds compared with the controls at the two sampling points post infection (A) OTUs 1 and 12, (B) OTUs 4 and 29. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
label | Figure 3 |
caption | Relative abundances (%) of the most relevant OTUs in the infected birds compared with the controls at the two sampling points post infection (A) OTUs 1 and 12, (B) OTUs 4 and 29. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
p | Relative abundances (%) of the most relevant OTUs in the infected birds compared with the controls at the two sampling points post infection (A) OTUs 1 and 12, (B) OTUs 4 and 29. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
sec | Assessment of the microbial community diversity Diversity indices estimating species richness and evenness for birds are shown in Figure 4. Diversity indices indicated that microbial richness and diversity increased with age. Interestingly, diversity indices were not different comparing samples from days 1 and 7. However, older chickens (14–28 days of age) had a significantly more diverse microbial community structure as indicated by the number of OTUs observed (Sobs), Chao1, ACE, Shannon's index, and Simpson index (P < 0.01). In addition, the microbial diversity in older chickens is more consistent, as there was no difference in diversity indices comparing samples from days 14 to 28. The results also revealed significant differences in the microbial diversity among jejunum and cecum as the chicken aged, supported by Sobs (P < 0.001), Chao1 (P < 0.001), ACE (P < 0.001), Shannon's index (P < 0.001), and Simpson index (P = 0.060) with a more complex diversity in the cecum compared with the jejunum. Furthermore, a difference in species richness among the luminal and mucosa-associated gut microbiota, independent of the age, was detected in all birds as supported by Sobs (P = 0.017), Chao1 (P = 0.015), ACE (P = 0.022), respectively. Figure 4 Species richness and diversity measures of the microbial community at all gut sites in the control (A), infected birds (B), and (C) species richness and diversity estimates for bacteria from cecum content of the infected birds compared with the controls. Left Y-axis for number of observed OTUs (Sobs), Chao 1 and ACE, and Right Y-axis for Shannon and Simpson. Significant differences were calculated with Kruskal-Wallis-tests and Mann-Whitney-tests, and significance was declared at P < 0.05. Data are presented as the mean values and SD. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. In the infected birds, significant differences in the microbial diversity among jejunum and cecum supported by Sobs (P < 0.001), Chao1 (P < 0.001), ACE (P < 0.001), Shannon's index (P < 0.001), and Simpson index (P = 0.011) were found. Additionally, an increase in the species richness among luminal and mucosa-associated gut microbiota of the infected birds at 14 dpi compared with those from 7 dpi was obtained. Diversity indices were not significantly different among the gut sites of infected and control birds. Exceptional to this, a higher species richness was noticed in the cecum content of infected birds at 14 dpi, supported by Sobs, Chao1, and ACE (P = 0.047, Figure 4C), indicating that the Campylobacter infection increased the microbiota complexity. |
title | Assessment of the microbial community diversity |
p | Diversity indices estimating species richness and evenness for birds are shown in Figure 4. Diversity indices indicated that microbial richness and diversity increased with age. Interestingly, diversity indices were not different comparing samples from days 1 and 7. However, older chickens (14–28 days of age) had a significantly more diverse microbial community structure as indicated by the number of OTUs observed (Sobs), Chao1, ACE, Shannon's index, and Simpson index (P < 0.01). In addition, the microbial diversity in older chickens is more consistent, as there was no difference in diversity indices comparing samples from days 14 to 28. The results also revealed significant differences in the microbial diversity among jejunum and cecum as the chicken aged, supported by Sobs (P < 0.001), Chao1 (P < 0.001), ACE (P < 0.001), Shannon's index (P < 0.001), and Simpson index (P = 0.060) with a more complex diversity in the cecum compared with the jejunum. Furthermore, a difference in species richness among the luminal and mucosa-associated gut microbiota, independent of the age, was detected in all birds as supported by Sobs (P = 0.017), Chao1 (P = 0.015), ACE (P = 0.022), respectively. |
figure | Figure 4 Species richness and diversity measures of the microbial community at all gut sites in the control (A), infected birds (B), and (C) species richness and diversity estimates for bacteria from cecum content of the infected birds compared with the controls. Left Y-axis for number of observed OTUs (Sobs), Chao 1 and ACE, and Right Y-axis for Shannon and Simpson. Significant differences were calculated with Kruskal-Wallis-tests and Mann-Whitney-tests, and significance was declared at P < 0.05. Data are presented as the mean values and SD. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
label | Figure 4 |
caption | Species richness and diversity measures of the microbial community at all gut sites in the control (A), infected birds (B), and (C) species richness and diversity estimates for bacteria from cecum content of the infected birds compared with the controls. Left Y-axis for number of observed OTUs (Sobs), Chao 1 and ACE, and Right Y-axis for Shannon and Simpson. Significant differences were calculated with Kruskal-Wallis-tests and Mann-Whitney-tests, and significance was declared at P < 0.05. Data are presented as the mean values and SD. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
p | Species richness and diversity measures of the microbial community at all gut sites in the control (A), infected birds (B), and (C) species richness and diversity estimates for bacteria from cecum content of the infected birds compared with the controls. Left Y-axis for number of observed OTUs (Sobs), Chao 1 and ACE, and Right Y-axis for Shannon and Simpson. Significant differences were calculated with Kruskal-Wallis-tests and Mann-Whitney-tests, and significance was declared at P < 0.05. Data are presented as the mean values and SD. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
p | In the infected birds, significant differences in the microbial diversity among jejunum and cecum supported by Sobs (P < 0.001), Chao1 (P < 0.001), ACE (P < 0.001), Shannon's index (P < 0.001), and Simpson index (P = 0.011) were found. Additionally, an increase in the species richness among luminal and mucosa-associated gut microbiota of the infected birds at 14 dpi compared with those from 7 dpi was obtained. Diversity indices were not significantly different among the gut sites of infected and control birds. Exceptional to this, a higher species richness was noticed in the cecum content of infected birds at 14 dpi, supported by Sobs, Chao1, and ACE (P = 0.047, Figure 4C), indicating that the Campylobacter infection increased the microbiota complexity. |
sec | Similarity and stability of the gut microbiota composition over time The microbial community similarity among all samples over time was assessed by calculating a Bray-Curtis similarity matrix. Community similarity analysis based on the Bray-Curtis index showed clear differences between gut sites and age, indicating strong shifts in microbial community structures (Figure 5). In addition, the Bray-Curtis index suggested that the birds at the first day of age displayed a high degree of dissimilarity compared with the other ages. It was also apparent that microbiota compositions of older birds were more similar compared with young birds. Figure 5 Microbial community similarity between all samples calculated with Bray-Curtis similarities, which displays the similarity results between the control and infected groups according to age and gut sites. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. The Bray-Curtis index revealed clear differences between jejunum and cecum from infected birds at the two sampling time points post infection. Furthermore, the comparison of the microbiota between control and infected birds showed that community structures were more dissimilar at the OTUs level, demonstrating that the gut microbial communities changed as a result of infection. To measure the similarity between microbial communities in all birds at different ages, principal component analysis (PCA) was performed (Figure 6). PCA analysis showed that there was a clear clustering of the birds at days 1 and 7 of age in the jejunum and cecum compared with the other days. In addition, the microbial community of the older chickens clustered with less variation compared to young birds. PCA plots also demonstrate that, the microbial community was more separated in the ceca than in the jejunum. Figure 6 Principal component analysis (PCA) was analyzed for the control (A) and infected birds (B). Orange (day 1), Red (day 7), Green (day 14), Blue (day 21), and Black (day 28). Each symbol indicates an individual bird. All PCA plots include the data of all samples; symbols not belonging to the sample group indicated in the header are displayed faded. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. To delineate the shared species among the groups, a Venn diagram displaying the overlaps between gut sites at different ages and groups was performed (Figure S3). The proportions of shared OTUs appear to be low at each gut site from day 1 to day 28 of age. These shared species, however, varied from one site to another. Furthermore, the analysis showed that only 399 OTUs (n = 1847 OTUs) were shared among the jejunal mucosa in the control and infected birds, while 745 OTUs (n = 2401 OTUs) were shared between the jejunal content in the control and infected birds at the two time points post infection (Figure 7A). In the cecal mucosa and the cecal content, the comparison revealed that only 2218 OTUs (n = 6736 OTUs) and 2617 OTUs (n = 6860 OTUs) were shared, among control and infected birds combining the two time points post infection (Figure 7B). These data demonstrated that 25–36% of the observed OTUs in the jejunum and cecum were shared between the control and infected birds, respectively. Figure 7 Venn diagrams showing the shared OTUs between the control and infected birds at different gut sites at the two sampling points post infection (A) jejunum; (B) cecum. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i); d, day. |
title | Similarity and stability of the gut microbiota composition over time |
p | The microbial community similarity among all samples over time was assessed by calculating a Bray-Curtis similarity matrix. Community similarity analysis based on the Bray-Curtis index showed clear differences between gut sites and age, indicating strong shifts in microbial community structures (Figure 5). In addition, the Bray-Curtis index suggested that the birds at the first day of age displayed a high degree of dissimilarity compared with the other ages. It was also apparent that microbiota compositions of older birds were more similar compared with young birds. |
figure | Figure 5 Microbial community similarity between all samples calculated with Bray-Curtis similarities, which displays the similarity results between the control and infected groups according to age and gut sites. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
label | Figure 5 |
caption | Microbial community similarity between all samples calculated with Bray-Curtis similarities, which displays the similarity results between the control and infected groups according to age and gut sites. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
p | Microbial community similarity between all samples calculated with Bray-Curtis similarities, which displays the similarity results between the control and infected groups according to age and gut sites. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
p | The Bray-Curtis index revealed clear differences between jejunum and cecum from infected birds at the two sampling time points post infection. Furthermore, the comparison of the microbiota between control and infected birds showed that community structures were more dissimilar at the OTUs level, demonstrating that the gut microbial communities changed as a result of infection. |
p | To measure the similarity between microbial communities in all birds at different ages, principal component analysis (PCA) was performed (Figure 6). PCA analysis showed that there was a clear clustering of the birds at days 1 and 7 of age in the jejunum and cecum compared with the other days. In addition, the microbial community of the older chickens clustered with less variation compared to young birds. PCA plots also demonstrate that, the microbial community was more separated in the ceca than in the jejunum. |
figure | Figure 6 Principal component analysis (PCA) was analyzed for the control (A) and infected birds (B). Orange (day 1), Red (day 7), Green (day 14), Blue (day 21), and Black (day 28). Each symbol indicates an individual bird. All PCA plots include the data of all samples; symbols not belonging to the sample group indicated in the header are displayed faded. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
label | Figure 6 |
caption | Principal component analysis (PCA) was analyzed for the control (A) and infected birds (B). Orange (day 1), Red (day 7), Green (day 14), Blue (day 21), and Black (day 28). Each symbol indicates an individual bird. All PCA plots include the data of all samples; symbols not belonging to the sample group indicated in the header are displayed faded. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
p | Principal component analysis (PCA) was analyzed for the control (A) and infected birds (B). Orange (day 1), Red (day 7), Green (day 14), Blue (day 21), and Black (day 28). Each symbol indicates an individual bird. All PCA plots include the data of all samples; symbols not belonging to the sample group indicated in the header are displayed faded. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
p | To delineate the shared species among the groups, a Venn diagram displaying the overlaps between gut sites at different ages and groups was performed (Figure S3). The proportions of shared OTUs appear to be low at each gut site from day 1 to day 28 of age. These shared species, however, varied from one site to another. |
p | Furthermore, the analysis showed that only 399 OTUs (n = 1847 OTUs) were shared among the jejunal mucosa in the control and infected birds, while 745 OTUs (n = 2401 OTUs) were shared between the jejunal content in the control and infected birds at the two time points post infection (Figure 7A). In the cecal mucosa and the cecal content, the comparison revealed that only 2218 OTUs (n = 6736 OTUs) and 2617 OTUs (n = 6860 OTUs) were shared, among control and infected birds combining the two time points post infection (Figure 7B). These data demonstrated that 25–36% of the observed OTUs in the jejunum and cecum were shared between the control and infected birds, respectively. |
figure | Figure 7 Venn diagrams showing the shared OTUs between the control and infected birds at different gut sites at the two sampling points post infection (A) jejunum; (B) cecum. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i); d, day. |
label | Figure 7 |
caption | Venn diagrams showing the shared OTUs between the control and infected birds at different gut sites at the two sampling points post infection (A) jejunum; (B) cecum. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i); d, day. |
p | Venn diagrams showing the shared OTUs between the control and infected birds at different gut sites at the two sampling points post infection (A) jejunum; (B) cecum. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content; control (c); infected (i); d, day. |
sec | Discussion The intestinal microbiota acts as a physical barrier for incoming pathogens and plays an important role in the host resistance against infections by both direct interactions with pathogenic bacteria via competitive exclusion, such as occupation of attachment sites or consumption of nutrient sources, and indirectly by influencing the immune system via production of antimicrobial substances (Sekirov et al., 2010). Development of the gut microbiota in chickens occurs immediately after hatching and by getting older, this microbiome becomes very diverse until it reaches a relatively stable dynamic state (Pan and Yu, 2014). Interactions of the intestinal microbiome with the host and certain microorganisms have profound effects on bird health, and are therefore of great importance for poultry production. Consequently, in the present study, the composition of the gut microbiota of chickens in a longitudinal study from day 1 to day 28 of age was analyzed and the differences between content and mucosa-associated gut microbiota were investigated. In order to extend the range of analyses comparisons were performed between control chickens and chickens infected at 14 days of age with C. jejuni. In this study, a high diversity of phyla (15 in the jejunal and 4 in the cecal mucosal samples) was found at day 1 of life, indicating a rapid intake of environmental organisms after birth. In addition, the composition of the gut microbiota differed substantially between young and older birds, with Proteobacteria being significantly more present at the first day of life and decreasing thereafter, whereas the Firmicutes were the predominant phylum in older birds. This is in agreement with Lu et al. (2003) who found that the gut is firstly colonized by the phylum Proteobacteria, particularly by the family Enterobacteriaceae. In older birds, the phylum Firmicutes mainly represented by Lachnospiraceae, Ruminococcaceae, Clostridiaceae, and Lactobacillaceae dominated. As a consequence, the chicken gut is firstly colonized by facultative aerobes which are substituted later on by anaerobes. Obviously, oxygen consumption by the aerobic bacteria alters the gut ecosystem toward more reducing conditions, which facilitates subsequent growth and colonization of the obligate anaerobes (Wise and Siragusa, 2007). Besides Proteobacteria and Firmicutes, also lower abundant phyla (e.g., Actinobacteria and Tenericutes) changed significantly with time, indicating high dynamics in the re-organization of the whole microbiome through time. Taken together, the present study revealed that the chicken gut is largely dominated by the phyla Proteobacteria and Firmicutes, with lower proportions of Actinobacteria, Bacteroidetes, and Tenericutes. Similarly, previous studies have also shown that Firmicutes, Bacterioidetes, and Proteobacteria are the most common phyla in the chicken ceca (Wei et al., 2013; Oakley et al., 2014; Sergeant et al., 2014). Interestingly, jejunal, and cecal microbiota were found to be distinct and certain acid-tolerant bacteria, mostly Acidobacteria, were present in the jejunum only. Altogether, the results demonstrated that the abundance of bacteria varied between the jejunum and the cecum, with some species more present in the jejunum (e.g., Acinetobacter and Acidobacteria) and others (e.g., Bacteroides and Clostridium) being predominant in the cecum of chickens. This and other variations can be explained by the fact that feed passes quickly through the foregut and is retained for hours in the hindgut. In addition, the small intestine is mainly responsible for food digestion and absorption, while the large intestine, especially the cecum, is responsible for microbial fermentation, further nutrient absorption and detoxification of substances that are harmful to the host (Gong et al., 2002). Chickens investigated in the current study had a high abundance of E. coli and E. faecalis (best type strain hits) in the first week of life which might potentially increase their resistance to other bacterial infections. E. coli, a facultative anaerobe bacterium, was the dominant species in the early life of chickens. Thus, a depletion of E. coli during the second week of life could potentially affect the host susceptibility to enteric pathogen infections, representing a key role for these gut microbiota in host resistance. This decrease in E. coli abundance has been attributed with a beginning dominance of anaerobes (Zhu and Joerger, 2003). It may be possible that such disturbances in the community structure allow a pathogen to colonize and proliferate. Anyhow, it remains hypothetical whether these diversity changes influence the susceptibility to pathogens and the outcome of infection. The current results revealed that E. coli, E. faecalis, C. paraputrificum, and C. sartagoforme (best type strain hits) were more predominant in the mucosa than in the lumen, suggesting significant implications for birds' health, considering that the mucosa-associated bacteria are of great importance in the host mucosal responses with consequences for the mucosal barrier (Ott et al., 2004). Despite the high prevalence of Campylobacter in chickens the mechanism of colonization in the gut is still poorly understood. The high bacterial load in the gut and the establishment of a latent infection characterized by continuous shedding indicates that Campylobacter in chickens can modify the microbiota composition. In the current study it could be shown that Campylobacter colonization shifted the two major phyla towards an enrichment of Firmicutes with concomitant reduction of Proteobacteria. Interestingly, a reverse correlation between Firmicutes and Proteobacteria was observed, suggesting a possible antagonistic interaction between these two phyla. According to Pan and Yu (2014) alterations in one phyla or species may not only affect the host directly, but can also disrupt the entire microbial community. Notably, bacterial taxa belonging to the phyla Firmicutes are known to be involved in the degradation of complex carbohydrates (not absorbed by the host) and in the production of SCFAs (Thibodeau et al., 2015). Thus, the SCFAs production by Firmicutes might, at least partially, explain their dominance in the infected birds, which have a high SCFAs requirement as a source of energy for C. jejuni to colonize the chicken gut. Furthermore, Brown et al. (2012) reported that members of the phylum Firmicutes can inhibit the growth of opportunistic pathogens, such as E. coli, which has also been shown in the present study. Besides these major shifts, also low abundant phyla (e.g., Actinobacteria and Tenericutes) were affected by the Campylobacter infection, which could also disequilibrate the microbiome composition. Similarly, Johansen et al. (2006) found in a denaturing gradient gel electrophoresis (DGGE) based experiment that C. jejuni colonization affected the development and complexity of the microbial communities of the ceca over 17 days of age. Furthermore, Qu et al. (2008) noted that the community structure of the cecal microbiome from the C. jejuni challenged chicken has greater diversity and evenness with a higher abundance of Firmicutes at the expense of the Bacteroidetes and other taxa. Sofka et al. (2015) also reported that Campylobacter carriage, assessed in samples from slaughter houses, was associated with moderate modulations of the cecal microbiome as revealed by an increase in Streptococcus and Blautia relative abundance in birds of 56 days of age, originating from different farms and production types. Recently, Thibodeau et al. (2015) found also that C. jejuni colonization induced a moderate alteration of the chicken cecal microbiome beta-diversity at 35 days of age. This study's results strongly suggest that the Campylobacter associated alterations of the gut microbiota were a direct effect due to the interaction of C. jejuni with the microbiota or a consequence of the host responses or even a combination of both (Barman et al., 2008; Mon et al., 2015). The obtained results indicate that the influence of a Campylobacter infection on microbial communities was more pronounced at 14 dpi than at 7 dpi. This could be explained by an increased load of Camplyobacter at the later time point as demonstrated in recent studies using the same C. jejuni strain (Awad et al., 2014, 2015a,b, 2016). We also found significant differences in the abundance of certain bacterial species in the infected birds compared with the controls. C. jejuni caused a significant decrease in E. coli (best type strain hit) in the microbiota of infected birds in both jejunum and cecum. This is in agreement with our previous study which showed that Campylobacter colonization decreased E. coli loads in the jejunum and cecum at 7 dpi and at 14 dpi, but increased E. coli translocation to the liver and spleen of the infected birds as determined by conventional bacteriology (Awad et al., 2016). Thus, the current results pointed out that the relative abundance of E. coli could be an important determinant of susceptibility for a Campylobacter infection in particular and Gram-negative pathogens in general. In contrast to the Campylobacter -E. coli interaction, it was found that the relative abundance of Clostridium spp. was higher in the infected birds compared with the negative controls, indicating a link between C. jejuni and Clostridium. This confirms data from an earlier study in which a positive correlation between high levels of Clostridium perfringens (>6 log) and the colonization of C. jejuni were found by real-time quantitative PCR (Skånseng et al., 2006; Thibodeau et al., 2015). This might be due to the fact that C. jejuni acts as a hydrogen sink leading to improved growth conditions for some Clostridia through increased fermentation (Kaakoush et al., 2014). This link can also be explained by the fact that the Clostridium organic acid production could be used by C. jejuni as an energy source. Furthermore, it was found that a Campylobacter infection induces excess mucous production in the intestine (Molnár et al., 2015) which consequently may enhance Clostridium proliferation due to the fact that an increase in mucin secretion in the gut provides an opportunity for Clostridium spp. to proliferate (M'Sadeq et al., 2015). Overall, the higher abundance of Campylobacter and Clostridium spp. might result in a higher endotoxin production with subsequent increase in intestinal permeability that facilitates the colonization and enhances bacterial translocation from the intestine to the internal organs, which is well in agreement with our pervious results (Awad et al., 2015a, 2016). Finally, the strong shifts in the bacterial microbiome in the current study might help to explain why a Campylobacter infection is age dependent and chickens in the field become mainly colonized at an age of two to 4 weeks (Newell and Fearnley, 2003; Conlan et al., 2007). In agreement with this, Bereswill et al. (2011) demonstrated that a shift of intestinal microbiota in humans was linked with an increased susceptibility for C. jejuni. Finally, Haag et al. (2012) demonstrated that C. jejuni colonization in mice depends on the microbiota of the host and vice versa and Campylobacter colonization induces a shift of the intestinal microbiota. This was also observed in the present study as community structures were more dissimilar at the OTUs level in the infected birds compared with the controls. Moreover, in the infected birds, the population of beneficial microbes, such as E. coli and E. desmolans were comparatively lower than the potentially pathogenic bacteria, such as Clostridium spp., rendering the need for modulation of the gut microbiota to improve the gut health of the infected birds. |
title | Discussion |
p | The intestinal microbiota acts as a physical barrier for incoming pathogens and plays an important role in the host resistance against infections by both direct interactions with pathogenic bacteria via competitive exclusion, such as occupation of attachment sites or consumption of nutrient sources, and indirectly by influencing the immune system via production of antimicrobial substances (Sekirov et al., 2010). Development of the gut microbiota in chickens occurs immediately after hatching and by getting older, this microbiome becomes very diverse until it reaches a relatively stable dynamic state (Pan and Yu, 2014). |
p | Interactions of the intestinal microbiome with the host and certain microorganisms have profound effects on bird health, and are therefore of great importance for poultry production. Consequently, in the present study, the composition of the gut microbiota of chickens in a longitudinal study from day 1 to day 28 of age was analyzed and the differences between content and mucosa-associated gut microbiota were investigated. In order to extend the range of analyses comparisons were performed between control chickens and chickens infected at 14 days of age with C. jejuni. |
p | In this study, a high diversity of phyla (15 in the jejunal and 4 in the cecal mucosal samples) was found at day 1 of life, indicating a rapid intake of environmental organisms after birth. In addition, the composition of the gut microbiota differed substantially between young and older birds, with Proteobacteria being significantly more present at the first day of life and decreasing thereafter, whereas the Firmicutes were the predominant phylum in older birds. This is in agreement with Lu et al. (2003) who found that the gut is firstly colonized by the phylum Proteobacteria, particularly by the family Enterobacteriaceae. In older birds, the phylum Firmicutes mainly represented by Lachnospiraceae, Ruminococcaceae, Clostridiaceae, and Lactobacillaceae dominated. As a consequence, the chicken gut is firstly colonized by facultative aerobes which are substituted later on by anaerobes. Obviously, oxygen consumption by the aerobic bacteria alters the gut ecosystem toward more reducing conditions, which facilitates subsequent growth and colonization of the obligate anaerobes (Wise and Siragusa, 2007). |
p | Besides Proteobacteria and Firmicutes, also lower abundant phyla (e.g., Actinobacteria and Tenericutes) changed significantly with time, indicating high dynamics in the re-organization of the whole microbiome through time. Taken together, the present study revealed that the chicken gut is largely dominated by the phyla Proteobacteria and Firmicutes, with lower proportions of Actinobacteria, Bacteroidetes, and Tenericutes. Similarly, previous studies have also shown that Firmicutes, Bacterioidetes, and Proteobacteria are the most common phyla in the chicken ceca (Wei et al., 2013; Oakley et al., 2014; Sergeant et al., 2014). |
p | Interestingly, jejunal, and cecal microbiota were found to be distinct and certain acid-tolerant bacteria, mostly Acidobacteria, were present in the jejunum only. Altogether, the results demonstrated that the abundance of bacteria varied between the jejunum and the cecum, with some species more present in the jejunum (e.g., Acinetobacter and Acidobacteria) and others (e.g., Bacteroides and Clostridium) being predominant in the cecum of chickens. This and other variations can be explained by the fact that feed passes quickly through the foregut and is retained for hours in the hindgut. In addition, the small intestine is mainly responsible for food digestion and absorption, while the large intestine, especially the cecum, is responsible for microbial fermentation, further nutrient absorption and detoxification of substances that are harmful to the host (Gong et al., 2002). |
p | Chickens investigated in the current study had a high abundance of E. coli and E. faecalis (best type strain hits) in the first week of life which might potentially increase their resistance to other bacterial infections. E. coli, a facultative anaerobe bacterium, was the dominant species in the early life of chickens. Thus, a depletion of E. coli during the second week of life could potentially affect the host susceptibility to enteric pathogen infections, representing a key role for these gut microbiota in host resistance. This decrease in E. coli abundance has been attributed with a beginning dominance of anaerobes (Zhu and Joerger, 2003). It may be possible that such disturbances in the community structure allow a pathogen to colonize and proliferate. Anyhow, it remains hypothetical whether these diversity changes influence the susceptibility to pathogens and the outcome of infection. |
p | The current results revealed that E. coli, E. faecalis, C. paraputrificum, and C. sartagoforme (best type strain hits) were more predominant in the mucosa than in the lumen, suggesting significant implications for birds' health, considering that the mucosa-associated bacteria are of great importance in the host mucosal responses with consequences for the mucosal barrier (Ott et al., 2004). |
p | Despite the high prevalence of Campylobacter in chickens the mechanism of colonization in the gut is still poorly understood. The high bacterial load in the gut and the establishment of a latent infection characterized by continuous shedding indicates that Campylobacter in chickens can modify the microbiota composition. In the current study it could be shown that Campylobacter colonization shifted the two major phyla towards an enrichment of Firmicutes with concomitant reduction of Proteobacteria. Interestingly, a reverse correlation between Firmicutes and Proteobacteria was observed, suggesting a possible antagonistic interaction between these two phyla. According to Pan and Yu (2014) alterations in one phyla or species may not only affect the host directly, but can also disrupt the entire microbial community. Notably, bacterial taxa belonging to the phyla Firmicutes are known to be involved in the degradation of complex carbohydrates (not absorbed by the host) and in the production of SCFAs (Thibodeau et al., 2015). Thus, the SCFAs production by Firmicutes might, at least partially, explain their dominance in the infected birds, which have a high SCFAs requirement as a source of energy for C. jejuni to colonize the chicken gut. Furthermore, Brown et al. (2012) reported that members of the phylum Firmicutes can inhibit the growth of opportunistic pathogens, such as E. coli, which has also been shown in the present study. |
p | Besides these major shifts, also low abundant phyla (e.g., Actinobacteria and Tenericutes) were affected by the Campylobacter infection, which could also disequilibrate the microbiome composition. Similarly, Johansen et al. (2006) found in a denaturing gradient gel electrophoresis (DGGE) based experiment that C. jejuni colonization affected the development and complexity of the microbial communities of the ceca over 17 days of age. Furthermore, Qu et al. (2008) noted that the community structure of the cecal microbiome from the C. jejuni challenged chicken has greater diversity and evenness with a higher abundance of Firmicutes at the expense of the Bacteroidetes and other taxa. Sofka et al. (2015) also reported that Campylobacter carriage, assessed in samples from slaughter houses, was associated with moderate modulations of the cecal microbiome as revealed by an increase in Streptococcus and Blautia relative abundance in birds of 56 days of age, originating from different farms and production types. Recently, Thibodeau et al. (2015) found also that C. jejuni colonization induced a moderate alteration of the chicken cecal microbiome beta-diversity at 35 days of age. |
p | This study's results strongly suggest that the Campylobacter associated alterations of the gut microbiota were a direct effect due to the interaction of C. jejuni with the microbiota or a consequence of the host responses or even a combination of both (Barman et al., 2008; Mon et al., 2015). The obtained results indicate that the influence of a Campylobacter infection on microbial communities was more pronounced at 14 dpi than at 7 dpi. This could be explained by an increased load of Camplyobacter at the later time point as demonstrated in recent studies using the same C. jejuni strain (Awad et al., 2014, 2015a,b, 2016). |
p | We also found significant differences in the abundance of certain bacterial species in the infected birds compared with the controls. C. jejuni caused a significant decrease in E. coli (best type strain hit) in the microbiota of infected birds in both jejunum and cecum. This is in agreement with our previous study which showed that Campylobacter colonization decreased E. coli loads in the jejunum and cecum at 7 dpi and at 14 dpi, but increased E. coli translocation to the liver and spleen of the infected birds as determined by conventional bacteriology (Awad et al., 2016). Thus, the current results pointed out that the relative abundance of E. coli could be an important determinant of susceptibility for a Campylobacter infection in particular and Gram-negative pathogens in general. |
p | In contrast to the Campylobacter -E. coli interaction, it was found that the relative abundance of Clostridium spp. was higher in the infected birds compared with the negative controls, indicating a link between C. jejuni and Clostridium. This confirms data from an earlier study in which a positive correlation between high levels of Clostridium perfringens (>6 log) and the colonization of C. jejuni were found by real-time quantitative PCR (Skånseng et al., 2006; Thibodeau et al., 2015). This might be due to the fact that C. jejuni acts as a hydrogen sink leading to improved growth conditions for some Clostridia through increased fermentation (Kaakoush et al., 2014). This link can also be explained by the fact that the Clostridium organic acid production could be used by C. jejuni as an energy source. Furthermore, it was found that a Campylobacter infection induces excess mucous production in the intestine (Molnár et al., 2015) which consequently may enhance Clostridium proliferation due to the fact that an increase in mucin secretion in the gut provides an opportunity for Clostridium spp. to proliferate (M'Sadeq et al., 2015). Overall, the higher abundance of Campylobacter and Clostridium spp. might result in a higher endotoxin production with subsequent increase in intestinal permeability that facilitates the colonization and enhances bacterial translocation from the intestine to the internal organs, which is well in agreement with our pervious results (Awad et al., 2015a, 2016). |
p | Finally, the strong shifts in the bacterial microbiome in the current study might help to explain why a Campylobacter infection is age dependent and chickens in the field become mainly colonized at an age of two to 4 weeks (Newell and Fearnley, 2003; Conlan et al., 2007). In agreement with this, Bereswill et al. (2011) demonstrated that a shift of intestinal microbiota in humans was linked with an increased susceptibility for C. jejuni. Finally, Haag et al. (2012) demonstrated that C. jejuni colonization in mice depends on the microbiota of the host and vice versa and Campylobacter colonization induces a shift of the intestinal microbiota. This was also observed in the present study as community structures were more dissimilar at the OTUs level in the infected birds compared with the controls. Moreover, in the infected birds, the population of beneficial microbes, such as E. coli and E. desmolans were comparatively lower than the potentially pathogenic bacteria, such as Clostridium spp., rendering the need for modulation of the gut microbiota to improve the gut health of the infected birds. |
sec | Conclusion In the current study a substantial change in the composition of luminal and mucosa-associated gut microbiota in broiler chickens from day 1–28 was noticed. It could also be demonstrated that a C. jejuni infection in chickens was associated with significant changes in the composition of the intestinal ecosystem. Furthermore, these changes of the gut microbiota could lead to intestinal dysfunction, which has been evidenced in our previous studies. In this context, the results provide new insights into the microecological divergence of the intestinal microbiota with and without a Campylobacter infection and illustrate the C. jejuni–host crosstalk within the gut of broiler chickens. Understanding the relationship between disruption of the normal gut microbiota and Campylobacter infection may lead to improve in control strategies in order to minimize the consequences for the chicken host and the risk of bacterial spread to humans. |
title | Conclusion |
p | In the current study a substantial change in the composition of luminal and mucosa-associated gut microbiota in broiler chickens from day 1–28 was noticed. It could also be demonstrated that a C. jejuni infection in chickens was associated with significant changes in the composition of the intestinal ecosystem. Furthermore, these changes of the gut microbiota could lead to intestinal dysfunction, which has been evidenced in our previous studies. In this context, the results provide new insights into the microecological divergence of the intestinal microbiota with and without a Campylobacter infection and illustrate the C. jejuni–host crosstalk within the gut of broiler chickens. Understanding the relationship between disruption of the normal gut microbiota and Campylobacter infection may lead to improve in control strategies in order to minimize the consequences for the chicken host and the risk of bacterial spread to humans. |
sec | Author contributions All authors listed, have made substantial, direct and intellectual contribution to the work, and approved it for publication. Conflict of interest statement The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. |
title | Author contributions |
p | All authors listed, have made substantial, direct and intellectual contribution to the work, and approved it for publication. |
sec | Conflict of interest statement The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. |
title | Conflict of interest statement |
p | The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. |
back | Part of this work was performed within the CEPO (Centre of Excellence for Poultry) project, which was funded by the European Regional Development Fund, Cross-border Cooperation Programme Austria–Hungary 2007–2013. Grant No: L00112. Our special acknowledgement to Dr. Alexander Tichy (Bioinformatics and Biostatistics Platform, Department of Biomedical Sciences, University of Veterinary Medicine Vienna) for his assistance with the statistical analyses. Furthermore, we would like to thank all staff who assisted with the animal infection experiments at the Clinic for Poultry and Fish Medicine, University of Veterinary Medicine Vienna. Supplementary material The Supplementary Material for this article can be found online at: http://journal.frontiersin.org/article/10.3389/fcimb.2016.00154/full#supplementary-material Figure S1 Relative abundances (%) of the most abundant bacterial phyla of (A) control and (B) infected birds. Data are presented as the mean values and SD. Left Y-axis for Firmicutes, Proteobacteria and others (unclassified); Right Y-axis for Tenericutes, Acidobacteria, Actinobacteria, Bacteroides, and Cyanobacteria. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. Click here for additional data file. Figure S2 Heatmap showing the relative abundances of the 50 most-abundant OTUs sorted by gut sites and age in the control birds. The heat map shows relative abundance of a given phylotype. Colour scaling is ranged from 0 to higher than 25%. n.d, not detected; n.a, not analyzed. Click here for additional data file. Figure S3 Venn diagrams are showing the shared OTUs for the control at different gut sites from day 1–28 (A) jejunum; (B) cecum. jm, jejunal mucosa; jc, jejunal content; cm, cecum mucosa; cc, cecum content; (c), control; (i), infected; d, day. Click here for additional data file. Table S1 Relative abundances (%) of bacterial phyla in the control birds from day 1–28 (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content. Click here for additional data file. Table S2 Relative abundances (%) of bacterial phyla in different gut sites of control birds (day 1–28). Click here for additional data file. Table S3 Relative abundances (%) of bacterial phyla in different gut sites of infected birds (days 21 and 28). Click here for additional data file. Table S4 Relative abundances (%) of bacterial phyla in the infected birds at the two sampling points post infection (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content. Click here for additional data file. Table S5 The 50 most abundant OTUs in the control birds from day 1–28 (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content. Click here for additional data file. Table S6 The 50 most abundant OTUs in the infected birds at the two sampling points post infection (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, and (D) cecal content. Click here for additional data file. |
ack | Part of this work was performed within the CEPO (Centre of Excellence for Poultry) project, which was funded by the European Regional Development Fund, Cross-border Cooperation Programme Austria–Hungary 2007–2013. Grant No: L00112. Our special acknowledgement to Dr. Alexander Tichy (Bioinformatics and Biostatistics Platform, Department of Biomedical Sciences, University of Veterinary Medicine Vienna) for his assistance with the statistical analyses. Furthermore, we would like to thank all staff who assisted with the animal infection experiments at the Clinic for Poultry and Fish Medicine, University of Veterinary Medicine Vienna. |
p | Part of this work was performed within the CEPO (Centre of Excellence for Poultry) project, which was funded by the European Regional Development Fund, Cross-border Cooperation Programme Austria–Hungary 2007–2013. Grant No: L00112. Our special acknowledgement to Dr. Alexander Tichy (Bioinformatics and Biostatistics Platform, Department of Biomedical Sciences, University of Veterinary Medicine Vienna) for his assistance with the statistical analyses. Furthermore, we would like to thank all staff who assisted with the animal infection experiments at the Clinic for Poultry and Fish Medicine, University of Veterinary Medicine Vienna. |
sec | Supplementary material The Supplementary Material for this article can be found online at: http://journal.frontiersin.org/article/10.3389/fcimb.2016.00154/full#supplementary-material Figure S1 Relative abundances (%) of the most abundant bacterial phyla of (A) control and (B) infected birds. Data are presented as the mean values and SD. Left Y-axis for Firmicutes, Proteobacteria and others (unclassified); Right Y-axis for Tenericutes, Acidobacteria, Actinobacteria, Bacteroides, and Cyanobacteria. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. Click here for additional data file. Figure S2 Heatmap showing the relative abundances of the 50 most-abundant OTUs sorted by gut sites and age in the control birds. The heat map shows relative abundance of a given phylotype. Colour scaling is ranged from 0 to higher than 25%. n.d, not detected; n.a, not analyzed. Click here for additional data file. Figure S3 Venn diagrams are showing the shared OTUs for the control at different gut sites from day 1–28 (A) jejunum; (B) cecum. jm, jejunal mucosa; jc, jejunal content; cm, cecum mucosa; cc, cecum content; (c), control; (i), infected; d, day. Click here for additional data file. Table S1 Relative abundances (%) of bacterial phyla in the control birds from day 1–28 (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content. Click here for additional data file. Table S2 Relative abundances (%) of bacterial phyla in different gut sites of control birds (day 1–28). Click here for additional data file. Table S3 Relative abundances (%) of bacterial phyla in different gut sites of infected birds (days 21 and 28). Click here for additional data file. Table S4 Relative abundances (%) of bacterial phyla in the infected birds at the two sampling points post infection (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content. Click here for additional data file. Table S5 The 50 most abundant OTUs in the control birds from day 1–28 (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content. Click here for additional data file. Table S6 The 50 most abundant OTUs in the infected birds at the two sampling points post infection (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, and (D) cecal content. Click here for additional data file. |
title | Supplementary material |
p | The Supplementary Material for this article can be found online at: http://journal.frontiersin.org/article/10.3389/fcimb.2016.00154/full#supplementary-material |
label | Figure S1 |
caption | Relative abundances (%) of the most abundant bacterial phyla of (A) control and (B) infected birds. Data are presented as the mean values and SD. Left Y-axis for Firmicutes, Proteobacteria and others (unclassified); Right Y-axis for Tenericutes, Acidobacteria, Actinobacteria, Bacteroides, and Cyanobacteria. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
p | Relative abundances (%) of the most abundant bacterial phyla of (A) control and (B) infected birds. Data are presented as the mean values and SD. Left Y-axis for Firmicutes, Proteobacteria and others (unclassified); Right Y-axis for Tenericutes, Acidobacteria, Actinobacteria, Bacteroides, and Cyanobacteria. JM, jejunal mucosa; JC, jejunal content; CM, cecum mucosa; CC, cecum content. |
caption | Click here for additional data file. |
p | Click here for additional data file. |
label | Figure S2 |
caption | Heatmap showing the relative abundances of the 50 most-abundant OTUs sorted by gut sites and age in the control birds. The heat map shows relative abundance of a given phylotype. Colour scaling is ranged from 0 to higher than 25%. n.d, not detected; n.a, not analyzed. |
p | Heatmap showing the relative abundances of the 50 most-abundant OTUs sorted by gut sites and age in the control birds. The heat map shows relative abundance of a given phylotype. Colour scaling is ranged from 0 to higher than 25%. n.d, not detected; n.a, not analyzed. |
caption | Click here for additional data file. |
p | Click here for additional data file. |
label | Figure S3 |
caption | Venn diagrams are showing the shared OTUs for the control at different gut sites from day 1–28 (A) jejunum; (B) cecum. jm, jejunal mucosa; jc, jejunal content; cm, cecum mucosa; cc, cecum content; (c), control; (i), infected; d, day. |
p | Venn diagrams are showing the shared OTUs for the control at different gut sites from day 1–28 (A) jejunum; (B) cecum. jm, jejunal mucosa; jc, jejunal content; cm, cecum mucosa; cc, cecum content; (c), control; (i), infected; d, day. |
caption | Click here for additional data file. |
p | Click here for additional data file. |
label | Table S1 |
caption | Relative abundances (%) of bacterial phyla in the control birds from day 1–28 (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content. |
p | Relative abundances (%) of bacterial phyla in the control birds from day 1–28 (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content. |
caption | Click here for additional data file. |
p | Click here for additional data file. |
label | Table S2 |
caption | Relative abundances (%) of bacterial phyla in different gut sites of control birds (day 1–28). |
p | Relative abundances (%) of bacterial phyla in different gut sites of control birds (day 1–28). |
caption | Click here for additional data file. |
p | Click here for additional data file. |
label | Table S3 |
caption | Relative abundances (%) of bacterial phyla in different gut sites of infected birds (days 21 and 28). |
p | Relative abundances (%) of bacterial phyla in different gut sites of infected birds (days 21 and 28). |
caption | Click here for additional data file. |
p | Click here for additional data file. |
label | Table S4 |
caption | Relative abundances (%) of bacterial phyla in the infected birds at the two sampling points post infection (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content. |
p | Relative abundances (%) of bacterial phyla in the infected birds at the two sampling points post infection (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content. |
caption | Click here for additional data file. |
p | Click here for additional data file. |
label | Table S5 |
caption | The 50 most abundant OTUs in the control birds from day 1–28 (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content. |
p | The 50 most abundant OTUs in the control birds from day 1–28 (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, (D) cecal content. |
caption | Click here for additional data file. |
p | Click here for additional data file. |
label | Table S6 |
caption | The 50 most abundant OTUs in the infected birds at the two sampling points post infection (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, and (D) cecal content. |
p | The 50 most abundant OTUs in the infected birds at the two sampling points post infection (A) jejunal mucosa, (B) jejunal content, (C) cecal mucosa, and (D) cecal content. |
caption | Click here for additional data file. |
p | Click here for additional data file. |
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