Evolutionary dynamics of the H7N9 avian influenza virus based on large-scale sequence analysis.

Since 2013, epidemics caused by novel H7N9 avian influenza A viruses (AIVs) have become a considerable public health issue. This study investigated the evolution of these viruses at the population level. Compared to H7 and N9 before 2013, there were 18 and 24 substitutions in the majority of novel H...

Full description

Bibliographic Details
Main Authors: Jiasheng Xiong, Ping Zhao, Pengfei Yang, Qingli Yan, Lufang Jiang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0220249
id doaj-835209ab908f481abda5fb33d466dc09
record_format Article
spelling doaj-835209ab908f481abda5fb33d466dc092021-03-03T19:50:35ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01148e022024910.1371/journal.pone.0220249Evolutionary dynamics of the H7N9 avian influenza virus based on large-scale sequence analysis.Jiasheng XiongPing ZhaoPengfei YangQingli YanLufang JiangSince 2013, epidemics caused by novel H7N9 avian influenza A viruses (AIVs) have become a considerable public health issue. This study investigated the evolution of these viruses at the population level. Compared to H7 and N9 before 2013, there were 18 and 24 substitutions in the majority of novel H7N9 AIVs, respectively. Nine of these in HA and six in NA were rare before 2013, and four of these in HA and two in NA displayed host tropism. S136(128)N and A143(135)V are located on the receptor binding sites of the HA1 subunit and might be important factors in determining the host species of novel H7N9 AIV. On an overall scale, the evolution of H7 and N9, both in terms of time distribution and host species, is under negative selection. However, both in HA and NA, several sites were under positive selection. In both the overall epidemics and the human-derived H7N9 AIVs, eight positive selection sites were identified in HA1, with some located within the known antigen epitopes or the receptor binding site(RBS) domain. This may induce variations in H7N9 AIV with positive selection. It is necessary to strengthen the surveillance of novel H7N9 AIVs, both in human and bird population to determine whether a new virus has emerged through selection pressure and to prevent future epidemics from occurring.https://doi.org/10.1371/journal.pone.0220249
collection DOAJ
language English
format Article
sources DOAJ
author Jiasheng Xiong
Ping Zhao
Pengfei Yang
Qingli Yan
Lufang Jiang
spellingShingle Jiasheng Xiong
Ping Zhao
Pengfei Yang
Qingli Yan
Lufang Jiang
Evolutionary dynamics of the H7N9 avian influenza virus based on large-scale sequence analysis.
PLoS ONE
author_facet Jiasheng Xiong
Ping Zhao
Pengfei Yang
Qingli Yan
Lufang Jiang
author_sort Jiasheng Xiong
title Evolutionary dynamics of the H7N9 avian influenza virus based on large-scale sequence analysis.
title_short Evolutionary dynamics of the H7N9 avian influenza virus based on large-scale sequence analysis.
title_full Evolutionary dynamics of the H7N9 avian influenza virus based on large-scale sequence analysis.
title_fullStr Evolutionary dynamics of the H7N9 avian influenza virus based on large-scale sequence analysis.
title_full_unstemmed Evolutionary dynamics of the H7N9 avian influenza virus based on large-scale sequence analysis.
title_sort evolutionary dynamics of the h7n9 avian influenza virus based on large-scale sequence analysis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description Since 2013, epidemics caused by novel H7N9 avian influenza A viruses (AIVs) have become a considerable public health issue. This study investigated the evolution of these viruses at the population level. Compared to H7 and N9 before 2013, there were 18 and 24 substitutions in the majority of novel H7N9 AIVs, respectively. Nine of these in HA and six in NA were rare before 2013, and four of these in HA and two in NA displayed host tropism. S136(128)N and A143(135)V are located on the receptor binding sites of the HA1 subunit and might be important factors in determining the host species of novel H7N9 AIV. On an overall scale, the evolution of H7 and N9, both in terms of time distribution and host species, is under negative selection. However, both in HA and NA, several sites were under positive selection. In both the overall epidemics and the human-derived H7N9 AIVs, eight positive selection sites were identified in HA1, with some located within the known antigen epitopes or the receptor binding site(RBS) domain. This may induce variations in H7N9 AIV with positive selection. It is necessary to strengthen the surveillance of novel H7N9 AIVs, both in human and bird population to determine whether a new virus has emerged through selection pressure and to prevent future epidemics from occurring.
url https://doi.org/10.1371/journal.pone.0220249
work_keys_str_mv AT jiashengxiong evolutionarydynamicsoftheh7n9avianinfluenzavirusbasedonlargescalesequenceanalysis
AT pingzhao evolutionarydynamicsoftheh7n9avianinfluenzavirusbasedonlargescalesequenceanalysis
AT pengfeiyang evolutionarydynamicsoftheh7n9avianinfluenzavirusbasedonlargescalesequenceanalysis
AT qingliyan evolutionarydynamicsoftheh7n9avianinfluenzavirusbasedonlargescalesequenceanalysis
AT lufangjiang evolutionarydynamicsoftheh7n9avianinfluenzavirusbasedonlargescalesequenceanalysis
_version_ 1714825447715373056