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Epidemiological characteristics and phylogenic analysis of human respiratory syncytial virus in patients with respiratory infections during 2011-2016 in southern China
Abstract
Background: Human respiratory syncytial virus (RSV) is one of the most important pathogens that cause acute respiratory infections in children and immunocompromised adults. This work was conducted to understand the epidemiological and phylogenetic features of RSV in southern China during 2011-2016. Methods: A total of 16 024 nasopharyngeal swabs were collected from patients with respiratory infections in 14 hospitals, and screened for RSV and seven other respiratory viruses using real-time PCR. Six hundred and twenty-three RSV-positive samples from 13 hospitals were further analyzed for subtypes. G gene sequencing and phylogenetic analysis were performed based on 46 RSV-A and 15 RSV-B strains. Results: RSV was detected in 9.5% of the 16 024 specimens, the highest among the eight respiratory viruses screened. Most of these specimens came from inpatients and children under 3 years of age. The incidence of RSV-A (9.4%) was higher than that of RSV-B (4.4%) in children (<15 years), but not in adults (0.64% vs. 0.58%). A 2-year RSV-A dominance followed by a 1-year RSV-B dominance pattern was found. The co-detection rate of RSV was 25.1%. The main prevalent genotypes were NA1, ON1, and BA9. The prevalent RSV-A genotype in 2011-2012 was NA1, close to Chongqing and Brazil, but a new Hong Kong ON1 genotype was introduced and became the prevalent genotype in Guangzhou in 2014-2015. Deduced amino acid sequence analysis confirmed the ongoing evolution and a high selection pressure of RSV-A and B strains, especially in RSV-A ON1 and NA1 genotypes. Conclusions: This study demonstrated the molecular epidemiological characteristics of RSV in patients with respiratory infections in southern China.
Human respiratory syncytial virus (RSV), an Orthopneumovirus belonging to the Pneumoviridae family, is one of the most important pathogens causing severe acute lower respiratory infections (ALRI) in children (Borchers et al., 2013) . Studies have shown that RSV is the most common cause of hospitalization among children under 2 years of age and is associated with significant morbidity and mortality (Borchers et al., 2013; Nair et al., 2010; Shi et al, 2017) . In elderly and immunocompromised adults or patients with preexisting diseases, the morbidity and mortality rates have been shown to be significantly higher in RSV-infected patients (Colosia et al., 2017) . Therefore, RSV-related respiratory tract infection is a major public health issue worldwide.
The clinical manifestations after RSV infection range from a mild upper respiratory tract infection to severe life-threatening lower respiratory tract involvement such as bronchiolitis, pneumonia, and croup, together with some common symptoms including fever, rhinorrhea, cough, and wheezing (Borchers et al., 2013) , which are not readily distinguished from those of other common respiratory virus infections. Although efforts to develop an RSV vaccine for all age groups began in the 1960s, no safe and effective vaccine is yet available, and antiviral treatment for RSV infection is currently also very limited, with treatments usually being supportive and symptomatic (Colosia et al., 2017) .
Although RSV has only one single serotype, it can be divided into two antigenic groups -RSV-A and RSV-Baccording to the antigenicity of the G protein (Mufson et al., 1985) . To date, 14 genotypes of RSV-A and 25 genotypes of RSV-B have been confirmed (Ren et al., 2015; Shobugawa et al., 2009) , suggesting that genetic variability and evolution of RSV exists. However, data concerning the molecular epidemiological characteristics of RSV subtypes are limited, and there are few reports about the epidemiological status and genotypic characteristics of RSV prevailing in patients with acute respiratory infections (ARI) in southern China (Liu et al., 2016) . This study was, therefore, performed to investigate the presence of RSV in pediatric (<15 years) and adult (!15 years) patients with ARI in Guangzhou. Specimens were collected from ARI patients during 2011-2016 and RSV was analyzed along with seven other common respiratory viruses. A phylogenetic analysis of RSV-A and RSV-B strains was performed in order to better understand the molecular epidemiological characteristics of RSV circulating in southern China.
Nasopharyngeal swabs were collected from pediatric and adult patients with ARI from January 2011 to December 2016 in 14 hospitals covering Guangdong Province, southern China. Inclusion criteria were as follows: fever (body temperature !37.5 C within 3 days, accompanied by one or more symptoms of ARI including cough, runny nose, sputum, and sore throat. Information including demographic data, case history, symptoms, and clinical results of each patient was collected simultaneously. RSV and seven common respiratory viruses were screened: influenza virus (Flu), parainfluenza virus (PIV), human metapneumovirus (HMPV), human coronavirus (HCoV), human adenovirus (HADV), human rhinovirus (HRV), and human bocavirus (HBoV).
Viral RNA and DNA were extracted from 200 ml nasopharyngeal swab using a QIAamp MiniElute Virus Spin Kit (Qiagen, Germany) according to the manufacturer's instructions. Reverse transcription of viral RNA was performed using the Thermo Scientific RevertAid First Strand cDNA Synthesis Kit (Thermo Scientific, USA).
Common respiratory viruses and RSV were screened by realtime PCR as described previously (Bonroy et al., 2007; Van de Pol et al., 2007; Xu et al., 2012; Zhang et al., 2018) . The primers and probes used in the screening are listed in the Supplementary Material Table S1 . The RSV-specific primers and probes (synthesized by Invitrogen, Life Technology, Shanghai, China) are listed in Table 1 . To detect RSV, samples were assayed in a 25-ml reaction mixture containing 5 ml of cDNA, 12.5 ml of 2 Â Universal Master Mix (Applied Biosystems, USA), 300 nM of the forward and reverse primers, respectively, and 200 nM of the probe, with the following procedure: 10 min at 95 C, followed by 45 cycles of 15 s at 95 C and 1 min at 60 C. For detection of the RSV subtypes, samples were assayed in a 20-ml reaction mixture containing 2 ml of cDNA, 10 ml 2 Â LightCycler 480 Probes Master (Roche, Switzerland), 100 nM of forward and reverse primer, respectively, and 100 nM of probe, with the procedure of 95 C for 10 min and 45 cycles of 95 C for 15 s, 55 C for 1 min.
The RSV-positive samples were selected and further analyzed for genotypes using a nested PCR. Four pairs of primers were designed for G gene amplification, as listed in Table 2 . The procedure for the first and the second round amplification of RSV-A was as follows: 95 C for 2 min, followed by 30 cycles of 94 C for 1 min, 50 C for 1 min, and 72 C for 1 min, and a final extension at 72 C for 10 min. The following procedure was used for the first and second round amplification of RSV-B: 95 C for 2 min, followed by 30 cycles of 94 C for 1 min, 50 C for 1 min, and 72 C for 2 min, and a final extension at 72 C for 7 min. The PCR products were purified by DNA purification kit (Takara, China) and cloned into vector PMD19-T (Takara, China). Sequencing was performed using a dideoxy chain termination method in both forward and reverse directions by Invitrogen Co., China. All PCR products used for cloning and sequencing were from three independent reactions.
A total of 61 strains from the years 2011-2015 were selected for G gene sequencing and phylogenetic analysis. The selection criteria were (1) the sample was available; (2) the sample was well preserved and the G gene could be successfully amplified. The G gene sequences were compared with those of the representative sequences of RSV-A and RSV-B from other countries or regions in GenBank, and were aligned by the Clustal X program. The phylogenetic tree of the RSV G gene was constructed by maximum-likelihood method with the Kimura 2-parameter model using MEGA 5.0 software. Bootstrap values were decided by 1000 replicates. The deduced amino acid sequences were analyzed with Bioedit software. Potential N-glycosylation sites (Asn-Xaa-Ser/ Thr, where Xaa is not a proline) were predicted using the NetNGlyc 1.0 Server (http://www.cbs.dtu.dk/services/NetNGlyc/).
IBM SPSS Statistics version 20.0 (IBM Corp., Armonk, NY, USA) was used for the statistical analysis. The incidence was calculated as the percentage of positive samples in the indicated total number of samples. The Chi-square test or Fisher's exact test was used to Table 1 Real-time PCR primers and probes used for the detection of the RSV subtypes.
Sequence ( evaluate the difference between rates. The odds ratio was calculated using the risk estimate of crosstabs Chi-square test in SPSS. The trend line was drawn by moving average method. A p-value of < 0.05 was considered statistically significant.
Among the 16 024 patients, 5818 (36.3%) were found to be positive for at least one virus and 771 (4.8%) were infected by more than one virus. The male to female ratio was 1.63 (9923/6106), and the inpatient to emergency/outpatient ratio was 2.95 (11 964/ 4060). Analysis of the RSV subtypes was performed on 623 RSVpositive swabs from 13 hospitals except Guangzhou Institute of Respiratory Diseases. The demographic and clinical characteristics of the 16 024 patients are shown in the Supplementary Material Table S2 . The patient composition and surveillance results for RSV and the seven other common respiratory viruses are shown in Table 3 . The monthly distributions are shown in Figure 1 and Supplementary Material Figure S1 .
Influenza virus was prevalent mainly in the spring, especially in February to May. Similarly, the epidemic of HMPV was mainly in the spring, especially in March to May, but in 2012, the epidemic season appeared earlier in the winter. PIV was mainly epidemic in spring and autumn, especially in 2011-2012. HRV was epidemic throughout the year; however, as most of the hospitals did not test for HRV in 2011, the incidence in that year was low. HBoV was epidemic mainly in summer during 2011-2014, but in 2015-2016, the epidemic peak appeared in autumn. HCoV and HADV were prevalent throughout the year. RSV was mainly epidemic in winter and spring, but in the summer of 2011 and 2013, the epidemic level was also high ( Figure 1A -H).
The age of the enrolled patients ranged from 0 days to 103 years, with a median age of 7 years. Among them, 33.8% (5419/16 024) were infants (<1 year) and toddlers (1-2 years). The age distributions of the patients with RSV and the seven other common respiratory viruses are shown in Figure 2 . For most of the viruses screened, the incidence in young children (3-5 years) was much higher than that in older children (6-14 years) and adults (!15 years), as shown in Fig. 2B -H, except for Flu, which was mostly detected in the 15-35 years group (row percentage 14.9%, Fig. 2A ). PIV and RSV mostly infected infants of 0-1 year (6.5% and 27.6%, respectively), and HBoV mostly infected those in the 1-2 years group (3.5%). For HADV and HMPV, the group with the highest incidence was 4-6 years (10.6%) and 2-3 years (4.0%), respectively. Similarly, HRV and HCoV tended to infect infants, with a high incidence of 7.4% and 4.0% respectively, and also children in the 3-4 years group (5.6% and 4.3%, respectively).
Among the 16 024 samples, 1514 (9.5%) were found to be RSVpositive, the highest among the eight respiratory viruses tested. The RSV-positive patients included 1389 inpatients and 125 outpatients, and the incidence was significantly higher in inpatients (91.7% vs. 8.3%, Chi-square = 257.86, p < 0.01). The odds ratio of infection with RSV resulting in severe disease or admission was 4.14 (95% confidence interval (CI) 3.43-4.98). Among the 1514 RSV-positive patients, 1039 (68.6%) were male and 475 (31.4%) were female; the difference was significant (Chi-square = 31.84, p < 0.01).
The common symptoms of RSV infection were cough (94.8%), fever (71.7%), runny nose (35.6%), and sputum (30.5%), which were not distinguishing from those of other common respiratory virus infections. Most of the RSV-positive patients (1432 cases, 94.6%) were children, including children not in nursery (59.5%), school Table 2 Primers used for RSV G gene amplification a .
Sequence
RSV, respiratory syncytial virus. a Sense primer: RSV-A-F or RSV-B-F; antisense primer: RSV-ABR. nursery children (17.5%), and primary and junior high school students (1.6%); the adult group were mainly retirees (1.3%). Infants and toddlers (<3 years) were the population with the highest risk of RSV infection, especially infants <1 year ( Figure 2H ). RSV-positive cases were distributed in eight hospitals. Guangzhou Institute of Respiratory Health showed the highest incidence in 2011-2013, but a notable epidemic peak appeared in Zhu Jiang Hospital in 2014 ( Figure 3A ). The annual distributions of RSV from 2011 to 2016 in Guangzhou are shown in Figure 3B . The RSV incidence was significantly lower in 2012 , and higher in 2011 .06, p < 0.01), showing epidemic peaks in 2011 and 2014-2015 in Guangzhou, respectively.
Among the 1514 RSV-positive samples, 623 from 13 hospitals were further analyzed for RSV-A/RSV-B subtypes; RSV subtyping was not performed at Guangzhou Institute of Respiratory Diseases. Among the 623 cases, 394 (63.2%) were RSV-A and 196 (31.5%) were RSV-B; both RSV-A and RSV-B were co-detected in three cases (0.5%), and 30 (4.8%) failed to be determined for specimen reasons. Among the 8936 ARI patients from 13 hospitals (excluding samples from Guangzhou Institute of Respiratory Diseases), the incidence of RSV-A was 4.4% and RSV-B was 2.2%. The three cases of RSV-A and B co-detection were all children (two were 2 years old and one was 5 months old) who were inpatients with ALRIs. The RSV-A incidence was 4.7% (258/5467) in males and 4.0% (139/ 3469) in females (Chi-square = 2.54, p > 0.05). However, the RSV-B incidence was 2.5% (139/5467) in males and 1.7% (60/3469) in females, with a significant difference (Chi-square = 6.44, p < 0.05). Both RSV-A and RSV-B mainly infected infants and toddlers, and the incidence of RSV-A (9.4%) was higher than that of RSV-B (4.4%) in children (Chi-square = 63.46, p < 0.01); however there was no difference in adults (0.64% vs. 0.58%, Chi-square = 0.15, p > 0.05; Figure 3C ).
The annual distribution trend for RSV-A was similar to that of the total RSV, with epidemic peaks in 2011 and 2014-2015 (Chi-square = 194.03, p < 0.01; Figure 3D ). In contrast, RSV-B was predominant in 2013 and 2016 (Chi-square = 168.19, p < 0.01; Figure RSV-A mainly circulated in winter and spring, with a peak in January to April and a lower peak in July to September ( Figure 4A ). RSV-B showed a 1-month stagger in epidemic peaks, with a later high peak in March to May and an earlier small peak in June to August ( Figure 4B ). RSV-A was the predominant subtype in most of the months except July, when RSV-B slightly exceeded ( Figure 4C ). On analysis of the detailed monthly distribution for 2011-2016 ( Figure 5) , it was found that most of the time, RSV-A and RSV-B had dominance alternately, except for January to June in 2014, when both RSV-A and RSV-B were epidemic at a high level. (Table 4) ; 91.1% were double infections (346/380) and 8.9% were triple infections (34/380). No correlation was found between co-detection and clinical symptoms. Among the 380 patients with co-detection, 232 was diagnosed as ALRI, not statistically higher than RSV single positive patients (232/380 vs. 745/1134, Chi-square = 2.68, p > 0.05). The age of patients with co-detection ranged from 0 to 87 years. Children <3 years were the most likely population to have RSV as a co-detection, accounting for 77.4% (294/380) of the co-detection cases, and 44.2% (168/380) were infants (<1 year). The co-detection rates were 25.6% in inpatients (355/1389) and 20.0% (25/125) in outpatients, with no significant difference between inpatients and emergency/outpatients (Chi-square = 1.88, p > 0.05). However, the co-detection rate in females was 28.6% (136/ 475), which was higher than the rate of 23.5% in males (244/1039, Chi-square = 4.59, p < 0.05).
To better understand the phylogenetic characteristics of RSV in southern China, 61 RSV strains, including 46 RSV-A and 15 RSV-B strains obtained in 2011-2015 in Guangzhou, were selected for G gene sequencing. Among the 46 RSV-A strains, 24 were selected 14) . Accordingly, two to four of the representative strains for each RSV-A and RSV-B genotype were selected from GenBank as reference strains.
Phylogenetic analysis showed that among the 46 Guangzhou RSV-A strains, there were 29 genotype NA1, 15 genotype ON1, one genotype NA3, and one genotype GA5 (Figures 6 and 7) . The 29 NA1 strains included 24 strains from 2011 and five strains from 2012. Among these, 25 were close to Chongqing NA1 strain GU550471, and the remaining four strains were in another cluster, closer to the Brazil strain JX513285. The 15 ON1 strains included eight 2015strains, five 2014 strains, one 2012 strain, and one 2013 strain, and all of them were close to Hong Kong ON1 strain KP221572. The NA3 strain was a 2015strain which was close to Beijing strain KC297277 and the GA5 strain was a 2014 strain close to Japan strain AB175815. All 15 Guangzhou strains of RSV-B belonged to the BA9 genotype and were close to Chengdu strain KT765074. Therefore, the main genotypes of RSV-A circulating in Guangzhou from 2011 to 2015 were NA1 and ON1, whereas the prevalent RSV-B genotype was BA9. Moreover, the dominant RSV-A genotype in 2011-2012 was NA1, but ON1 became the dominant genotype in 2014-2015 ( Figure 6 ).
The deduced amino acid sequences (according to the second hypervariable region of the G protein) of the 46 RSV-A and 15 RSV-B Guangzhou strains were aligned and compared with the RSV-A prototype strain A2, representative NA1, ON1, NA3, GA5 strains and ETLHSTTSEGYLSPSQVYTTSGQE) . Compared to the A2 prototype, ON1 subtype-specific substitutions (S222P, T253K, and S314L) were observed in all of the ON1 subtypes, and E232G was observed in most of the ON1 strains except GZ/2014/05. M286E, P310L, and S314P were observed in all NA1 strains. Other commonly observed substitutions for RSV-A strains included L208I, P215S, S222P, N237D/Y, T249I, N251Y, E262K, N297Y, P298L, and P320T. There were two deletions (L265 and E308) observed in GZ/2015/16. The analysis of potential N-glycosylation sites revealed that due to the N237Y substitution of ON1 and NA3 genotype, GZ/2015/16 and GZ/2015/10 lost potential N-glycosylation sites at residue 237, but interestingly, due to the D237N substitution, 10 Guangzhou NA1 strains regained this N-glycosylation site. Moreover, due to N318Y, T319A, or T320S/I/P mutation, eight Guangzhou NA1 and one Guangzhou NA3 strains lost the potential N-glycosylation site at residue 318 ( Figure 8 ). Compared to the sequences of the representative BA1 strain (BA4128/99B; Fan et al., 2017; Trento et al., 2003) , all BA9 strains had K218T, L223P, and S247P substitutions. I281T and H287Y existed in most of the Guangzhou BA9 strains except GZ2012/03 and GZ/2012/15, respectively. Besides the I281A substitution, GZ/ 2012/03 strain showed a loss of amino acids 254-273 (i.e., TTTSKHTERDTSTSQSIALD). Other commonly observed substitutions for RSV-B strains included P216S/L, I229T, T254I, T275I, and S304P. Due to T312P substitution, three Guangzhou BA9 strains lost potential N-glycosylation sites at residue 310 ( Figure 9 ).
RSV is one of the most common pathogens that cause ALRI, especially in young children . Since there is no specific drug and no effective vaccine for RSV infection, the long-term monitoring of RSV is important for RSV prevention and controlby continuously collecting and analyzing data related to RSV introduction, transmission, distribution, and variation, and by understanding more about RSV epidemic and variation patterns, we can predict the prevalent level and scale of RSV and help to produce control and prevention strategies. This study investigated the molecular epidemiological characteristics of RSV and its subtypes in ARI patients during 2011-2016 in Guangzhou, southern China. Since RSV usually co-infects with other respiratory viruses, seven common respiratory viruses including Flu, PIV, HCoV, HADV, HBoV, HMPV, and HRV were detected simultaneously.
The results showed that among the eight common respiratory viruses, RSV was the one most commonly detected, with a detection rate of 9.5% in 16 024 patients with ARI from 14 hospitals during 2011-2016 in southern China. Flu was the second most frequently detected respiratory virus (9.3%). The age characteristics and monthly distribution of RSV and the seven respiratory viruses in Guangzhou during 2011-2016 were consistent with those in previous reports (Liu et al., 2014; Zhang et al., 2014) . A total of 1514 patients were RSV-positive, 91.7% of whom were inpatients, significantly higher than outpatients (p < 0.01). The odds ratio of hospitalized patients with RSV infection to outpatient/emergency was 4.14, indicating that RSV infection has a considerable risk of resulting in severe disease. Infants and toddlers (<3 years) not in nursery (59.5%) seemed to have the highest risk of RSV infection, and the reason may lie in the decrease in maternal protective antibodies and the increase in exposure opportunities to crowds. The monthly distribution confirmed that RSV was mainly prevalent in winter and spring, consistent with other regions (Bashir et al., 2017; Slovic et al., 2016) . The annual distribution of RSV during 2011-2016 in Guangzhou revealed high epidemic years for 2011, 2014, and 2015, with year 2015 as an epidemic peak. There may be a biennial high incidence pattern of RSV in Guangzhou, and surveillance over a longer period will confirm the annual distribution characteristics (Esposito et al., 2015; Xiang et al., 2013) .
To better understand the epidemiological characteristics of RSV subtypes, RSV-A and RSV-B subtypes were determined based on 623 RSV-positive samples from 13 hospitals. The results showed that RSV-A was the dominant subtype circulating in Guangzhou during 2011-2016, consistent with reports from other regions (Hu et al., 2017; Slovic et al., 2016) . The three patients with co-detection were all infants and toddlers and inpatients with ALRI, and none of them died. It cannot be deduced whether the co-detection of both subtypes exacerbates the disease based on the symptoms. Both RSV-A and RSV-B mainly infected young children under 3 years of age, and the incidence of RSV-A was higher than that of RSV-B in children (p < 0.01), but not in adults (p > 0.05), indicating that RSV-A may have a higher pathogenicity to children.
The annual distribution of RSV subtypes revealed an interesting year distribution, as a 2-year RSV-A dominance followed by a 1-year RSV-B dominance pattern was found. A similar year distribution pattern has been reported previously in Beijing and Belgium, among others (Xiang et al., 2013; Coggins et al., 1998; Zlateva et al., 2007; Scott et al., 2004) . In addition to this pattern, RSV-A has been reported to show an epidemic for 2-4 years followed by RSV-B for 1 year pattern, as reported in Uruguay (Arbiza et al., 2005) ; and also, an RSV-A epidemic for 4 years followed by RSV-B for 1 year pattern, as reported in Japan (Shobugawa et al., 2009 ). It appears that this is the first time such a year distribution characteristic of RSV subtypes has been reported for Guangzhou. Most of the time, RSV-A and RSV-B took dominance alternately, but in January to June 2014, both RSV-A and RSV-B were epidemic at a high level. The co-detection rate of RSV was as high as 25.1% in Guangzhou from 2011 to 2016, and 91.1% of them were double infections and 8.9% were triple infections. Table 4 Cases of co-detection of RSV and seven other common respiratory viruses (Flu, PIV, HMPV, HCoV, HADV, HRV, and HBoV Influenza virus was the most common co-detected virus. No correlation was found between clinical symptoms and co-detection (p > 0.05), indicating that co-detection may not aggravate the disease or enhance the mortality of patients. However, this finding may be limited by the small sample size and the heterogeneity of co-detected viruses, and more studies will be needed to elucidate the relationships between RSV co-infection and disease severity. Of the 46 Guangzhou RSV-A strains, 29 strains belonged to genotype NA1, 15 belonged to genotype ON1, one belonged to genotype NA3, and one belonged to genotype GA5.
The genome of RSV encodes 11 proteins, including NS1, NS2, N, P, M, SH, G, F, M2-1, M2-2, and L (Cane, 2001) . According to the genetic diversity, RSV is genotyped mainly by the second highvariant region of the G protein C-terminal (HVR2) (Schobel et al., 2016) . Therefore, to better understand the phylogenetic characteristics of RSV in southern China and to gain more insight into RSV variation, we further analyzed the sequences of the G genes of the Guangzhou RSV strains. Most of the RSV-A genotypes from Guangzhou were close to Chongqing and Hong Kong strains and the RSV-B was close to a Chengdu strain. The prevalent RSV-B genotype in Guangzhou during 2011-2016 was BA9, whereas the prevalent RSV-A genotypes were more diverse. Among the 30 strains from the years 2011-2012, 29 were NA1 and one was ON1. Among the 15 strains from the years 2014-2015, 13 were ON1 and the other two were GA5 and BA9, respectively. The 2013 strain belonged to ON1. It can be seen that the NA1 genotype of RSV-A was prevalent in 2011-2012, while ON1 became the prevalent genotype in 2014-2015, which is consistent with the report of Fan et al. (2017) .
Deduced amino acid sequence analysis confirmed the ongoing evolution of RSV-A and B strains, especially in RSV-A ON1 and NA1 genotypes. Multiple highly variable substitutions were observed, and moreover, three Guangzhou ON1 strains showed the loss of a 24-amino acid fragment in the duplication region, and one BA9 strain had a 20-amino acid deletion. N-glycosylation site changes were also commonly observed in Guangzhou RSV-A strains, including the loss of the 251 and 318 glycosylation sites and regain of the 237 glycosylation site in most of the NA1 strains, and the loss of the 237 glycosylation site and two single amino acid deletions in an ON1 strain GZ/2015/16. Glycosylation site changes were also observed in three RSV-B BA9 strains. These mutations indicated a high selection pressure.
Since 2014-2015 was also the highest epidemic year for RSV-A, it was deduced that before 2012, the prevalent RSV genotype was NA1 from Chongqing, but in 2014, due to staff turnover, a new Hong Kong strain of ON1 genotype was introduced (Song et al., 2017) , evolved, and became the dominant strain. Furthermore, because the population lacked antibody protection, the new genotype spread rapidly and caused the high incidence of RSV-A in 2014-2015 in Guangzhou. Combined with the monthly distribution by site, we believe that the epidemic peaks in Zhu Jiang Hospital and Guangzhou Institute of Respiratory Diseases in 2014 reflected the prevalence of the new genotype. Although Zou et al. (2016) also investigated the evolution and transmission of RSV-A in Guangdong in 2008-2015, the present study is the first to report the introduction, evolution, and transmission of the new ON1 genotype in Guangzhou, southern China. Further studies should be conducted to reveal the mechanisms behind the emergence of new genotypes and RSV epidemic.
In conclusion, this study investigated the molecular epidemiological characteristics of RSV and its genotypes in children and adult patients with ARI in southern China during 2011-2016. The findings may have significance in guiding policy-making for RSV prevention and control, and may provide important information for RSV variation studies.
All studies involving human participants were approved by the Medical Ethics Review Board of Zhongshan School of Medicine, Sun Yat-sen University, in accordance with the guidelines for the protection of human subjects. Written informed consent was obtained from all participants or their guardians after being informed about the aims of the research and the right to keep their information confidential.
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