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Accelerated Evolution of H7N9 Subtype Influenza Virus under Vaccination Pressure

No avian H7N9 outbreaks have occurred since the introduction of H7N9 inactivated vaccine in the fall of 2017. However, H7N9 is still prevalent in poultry. To surveil the prevalence, genetic characteristics, and antigenic changes of H7N9, over 7000 oropharyngeal and cloaca swab specimens were collect...

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Autores principales: Wu, Yifan, Hu, Jingkai, Jin, Xuanjiang, Li, Xiao, Wang, Jinfeng, Zhang, Mengmeng, Chen, Jianglin, Xie, Shumin, Qi, Wenbao, Liao, Ming, Jia, Weixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112217/
https://www.ncbi.nlm.nih.gov/pubmed/33974230
http://dx.doi.org/10.1007/s12250-021-00383-x
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author Wu, Yifan
Hu, Jingkai
Jin, Xuanjiang
Li, Xiao
Wang, Jinfeng
Zhang, Mengmeng
Chen, Jianglin
Xie, Shumin
Qi, Wenbao
Liao, Ming
Jia, Weixin
author_facet Wu, Yifan
Hu, Jingkai
Jin, Xuanjiang
Li, Xiao
Wang, Jinfeng
Zhang, Mengmeng
Chen, Jianglin
Xie, Shumin
Qi, Wenbao
Liao, Ming
Jia, Weixin
author_sort Wu, Yifan
collection PubMed
description No avian H7N9 outbreaks have occurred since the introduction of H7N9 inactivated vaccine in the fall of 2017. However, H7N9 is still prevalent in poultry. To surveil the prevalence, genetic characteristics, and antigenic changes of H7N9, over 7000 oropharyngeal and cloaca swab specimens were collected from live poultry markets and farms in 15 provinces of China from 2017 to 2019. A total of 85 influenza virus subtype H7N9 strains were isolated and 20 representative strains were selected for genetic analysis and antigenicity evaluation. Results indicated the decreased prevalence of low-pathogenic H7N9 strains while highly-pathogenic H7N9 strains became dominated since the introduction of vaccine. Phylogenetic analysis showed that strains from 2019 formed an independent small branch and were genetically distant to strains isolated in 2013–2018. Analysis of key amino acid sites showed that the virus strains may adapt to the host environment evolutionally through mutation. Our analysis predicted additional potential glycosylation sites for HA and NA genes in the 2019 strains. Sequence analysis of HA gene in strains isolated from 2018 to 2019 showed that there were an increased nucleotide substitution rate and an increased mutation rate in the first and second nucleotides of coding codons within the open reading frame. The hemagglutination inhibition (HI) assay showed that H7-Re1 and H7-Re2 exhibited a lower HI titer for isolates from 2019, while H7-Re3 and rLN79 showed a high HI titer. The protective effect of the vaccine decreased after 15 months of use. Overall, under vaccination pressure, the evolution of influenza virus subtype H7N9 has accelerated. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12250-021-00383-x.
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spelling pubmed-81122172021-05-12 Accelerated Evolution of H7N9 Subtype Influenza Virus under Vaccination Pressure Wu, Yifan Hu, Jingkai Jin, Xuanjiang Li, Xiao Wang, Jinfeng Zhang, Mengmeng Chen, Jianglin Xie, Shumin Qi, Wenbao Liao, Ming Jia, Weixin Virol Sin Research Article No avian H7N9 outbreaks have occurred since the introduction of H7N9 inactivated vaccine in the fall of 2017. However, H7N9 is still prevalent in poultry. To surveil the prevalence, genetic characteristics, and antigenic changes of H7N9, over 7000 oropharyngeal and cloaca swab specimens were collected from live poultry markets and farms in 15 provinces of China from 2017 to 2019. A total of 85 influenza virus subtype H7N9 strains were isolated and 20 representative strains were selected for genetic analysis and antigenicity evaluation. Results indicated the decreased prevalence of low-pathogenic H7N9 strains while highly-pathogenic H7N9 strains became dominated since the introduction of vaccine. Phylogenetic analysis showed that strains from 2019 formed an independent small branch and were genetically distant to strains isolated in 2013–2018. Analysis of key amino acid sites showed that the virus strains may adapt to the host environment evolutionally through mutation. Our analysis predicted additional potential glycosylation sites for HA and NA genes in the 2019 strains. Sequence analysis of HA gene in strains isolated from 2018 to 2019 showed that there were an increased nucleotide substitution rate and an increased mutation rate in the first and second nucleotides of coding codons within the open reading frame. The hemagglutination inhibition (HI) assay showed that H7-Re1 and H7-Re2 exhibited a lower HI titer for isolates from 2019, while H7-Re3 and rLN79 showed a high HI titer. The protective effect of the vaccine decreased after 15 months of use. Overall, under vaccination pressure, the evolution of influenza virus subtype H7N9 has accelerated. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12250-021-00383-x. Springer Singapore 2021-05-11 /pmc/articles/PMC8112217/ /pubmed/33974230 http://dx.doi.org/10.1007/s12250-021-00383-x Text en © Wuhan Institute of Virology, CAS 2021
spellingShingle Research Article
Wu, Yifan
Hu, Jingkai
Jin, Xuanjiang
Li, Xiao
Wang, Jinfeng
Zhang, Mengmeng
Chen, Jianglin
Xie, Shumin
Qi, Wenbao
Liao, Ming
Jia, Weixin
Accelerated Evolution of H7N9 Subtype Influenza Virus under Vaccination Pressure
title Accelerated Evolution of H7N9 Subtype Influenza Virus under Vaccination Pressure
title_full Accelerated Evolution of H7N9 Subtype Influenza Virus under Vaccination Pressure
title_fullStr Accelerated Evolution of H7N9 Subtype Influenza Virus under Vaccination Pressure
title_full_unstemmed Accelerated Evolution of H7N9 Subtype Influenza Virus under Vaccination Pressure
title_short Accelerated Evolution of H7N9 Subtype Influenza Virus under Vaccination Pressure
title_sort accelerated evolution of h7n9 subtype influenza virus under vaccination pressure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112217/
https://www.ncbi.nlm.nih.gov/pubmed/33974230
http://dx.doi.org/10.1007/s12250-021-00383-x
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