Id |
Subject |
Object |
Predicate |
Lexical cue |
T176 |
0-4 |
Sentence |
denotes |
3.5. |
T177 |
5-62 |
Sentence |
denotes |
Influenza D Viruses Use Neu5,9Ac2 and Neu5Gc9Ac Receptors |
T178 |
63-401 |
Sentence |
denotes |
In 2011, a novel virus isolated from a nasal swab of a 15-week-old pig with influenza-like symptoms in Oklahoma in the USA was found to possess seven (-)ssRNA genomic segments and HEF spike glycoproteins and to share approximately 50% overall aa sequence identity with human ICVs, and it was named C/swine/Oklahoma/1334/2011 (C/OK) [183]. |
T179 |
402-667 |
Sentence |
denotes |
At first, it was suggested to be a new subtype of ICVs due to (i) no cross-reaction of C/OK with human ICVs determined by hemagglutination inhibition assays and (ii) a wider cellular tropism of C/OK than that of a human ICV determined by cell culture studies [183]. |
T180 |
668-946 |
Sentence |
denotes |
In 2016, however, it was determined by the International Committee on Taxonomy of Viruses that this novel influenza virus is distinct from other types, and it was officially classified in a new genus, Deltainfluenzavirus, and so-called influenza D virus (IDV, type (species) D). |
T181 |
947-1420 |
Sentence |
denotes |
As shown in Table 1, in addition to pigs, IDVs have been isolated from cattle and have so far been classified into three lineages: D/OK (D/swine/Oklahoma/1334/2011-like viruses), D/660 (D/bovine/Oklahoma/660/2013-like viruses) and D/Japanese, with D/Japanese lineage being further classified into 2 sublineages, D/Yama2016 (D/bovine/Yamagata/10710/2016-like viruses) and D/Yama2019 (D/bovine/Yamagata/1/2019-like viruses), based on phylogenetic and antigenic analyses [73]. |
T182 |
1421-1617 |
Sentence |
denotes |
Although there has been only serological evidence suggesting that IDV can infect humans [15], the virus may acquire mutations to potentially infect humans and to cause influenza illness in humans. |
T183 |
1618-1711 |
Sentence |
denotes |
The host range of IVs is primarily determined by receptor binding specificity of the viruses. |
T184 |
1712-1846 |
Sentence |
denotes |
Recently, Liu et al. compared receptor binding specificities of IDVs and their related ICVs by a sialoglycan microarray approach [72]. |
T185 |
1847-2177 |
Sentence |
denotes |
Strain D/swine/Oklahoma/1334/2011 (D/OK) showed preferential binding to Neu5,9Ac2 and Neu5Gc9Ac either linked to α2,6Gal or α2,3Gal and strain D/bovine/Oklahoma/660/2013 /660) preferred to bind to Neu5,9Ac2α2,6Gal, Neu5Gc9Acα2,6Gal and Neu5Gc9Acα2,3Gal, whereas strain C/Johannesburg/1/1966 dominantly recognized Neu5,9Ac2α2,6Gal. |
T186 |
2178-2313 |
Sentence |
denotes |
The broader receptor recognition by IDVs than by human ICV could explain why cellular tropism of IDVs is wider than that of human ICVs. |
T187 |
2314-2469 |
Sentence |
denotes |
Binding of IDVs to both Neu5,9Ac2 and Neu5Gc9Ac, different from human ICV binding to Neu5,9Ac2, could be determined by their different HEF-binding pockets. |
T188 |
2470-2847 |
Sentence |
denotes |
It was shown that different from human ICV HEF of C/Johannesburg/1/1966, swine IDV HEF of D/OK has an open cavity between the 230-helix and 270-loop in the receptor-binding site, which is thought to allow for accommodation of diverse glycan receptors, including Neu5Gc9Ac harboring an extra hydroxyl group on the N-acetyl group of C5 Neu5Gc and different sialyl linkages [184]. |
T189 |
2848-3022 |
Sentence |
denotes |
Further investigation of the structure of the bovine IDV HEF-binding pocket might lead to an understanding of different receptor binding preferences of swine and bovine IDVs. |
T190 |
3023-3136 |
Sentence |
denotes |
Receptor binding specificity of viruses is believed to be associated with receptors present on the target tissue. |
T191 |
3137-3329 |
Sentence |
denotes |
Glycoconjugate structures terminated with Neu5,9Ac2 and Neu5Gc9Ac along the bovine, porcine and human respiratory tracts have not been determined and further investigation is therefore needed. |
T192 |
3330-3666 |
Sentence |
denotes |
Previous findings that there is no Neu5Gc production in healthy humans due to mutation of a gene encoding CMP-Neu5Ac hydroxylase, which converts CMP-Neu5Ac to CMP-Neu5Gc [42,185], could explain why human ICVs prefer binding to Neu5,9Ac2, whereas swine and bovine IDVs can bind preferentially to both Neu5,9Ac2 and 9-O-acetylated Neu5Gc. |