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Genetic and biological characteristics of avian influenza virus subtype H1N8 in environments related to live poultry markets in China

BACKGROUND: Since 2008, avian influenza surveillance in poultry-related environments has been conducted annually in China. Samples have been collected from environments including live poultry markets, wild bird habitats, slaughterhouses, and poultry farms. Multiple subtypes of avian influenza virus...

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Autores principales: Zhang, Ye, Dong, Jie, Bo, Hong, Dong, Libo, Zou, Shumei, Li, Xiyan, Shu, Yuelong, Wang, Dayan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6532177/
https://www.ncbi.nlm.nih.gov/pubmed/31117981
http://dx.doi.org/10.1186/s12879-019-4079-z
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author Zhang, Ye
Dong, Jie
Bo, Hong
Dong, Libo
Zou, Shumei
Li, Xiyan
Shu, Yuelong
Wang, Dayan
author_facet Zhang, Ye
Dong, Jie
Bo, Hong
Dong, Libo
Zou, Shumei
Li, Xiyan
Shu, Yuelong
Wang, Dayan
author_sort Zhang, Ye
collection PubMed
description BACKGROUND: Since 2008, avian influenza surveillance in poultry-related environments has been conducted annually in China. Samples have been collected from environments including live poultry markets, wild bird habitats, slaughterhouses, and poultry farms. Multiple subtypes of avian influenza virus have been identified based on environmental surveillance, and an H1N8 virus was isolated from the drinking water of a live poultry market. METHODS: Virus isolation was performed by inoculating influenza A-positive specimens into embryonated chicken eggs. Next-generation sequencing was used for whole-genome sequencing. A solid-phase binding assay was performed to test the virus receptor binding specificity. Trypsin dependence plaque formation assays and intravenous pathogenicity index tests were used to evaluate virus pathogenicity in vitro and in vivo, respectively. Different cell lines were chosen for comparison of virus replication capacity. RESULTS: According to the phylogenetic trees, the whole gene segments of the virus named A/Environment/Fujian/85144/2014(H1N8) were of Eurasian lineage. The HA, NA, PB1, and M genes showed the highest homology with those of H1N8 or H1N2 subtype viruses isolated from local domestic ducks, while the PB2, PA, NP and NS genes showed high similarity with the genes of H7N9 viruses detected in 2017 and 2018 in the same province. This virus presented an avian receptor binding preference. The plaque formation assay showed that it was a trypsin-dependent virus. The intravenous pathogenicity index (IVPI) in chickens was 0.02. The growth kinetics of the A/Environment/Fujian/85144/2014(H1N8) virus in different cell lines were similar to those of a human-origin virus, A/Brisbane/59/2007(H1N1), but lower than those of the control avian-origin and swine-origin viruses. CONCLUSIONS: The H1N8 virus was identified in avian influenza-related environments in China for the first time and may have served as a gene carrier involved in the evolution of the H7N9 virus in poultry. This work further emphasizes the importance of avian influenza virus surveillance, especially in live poultry markets (LPMs). Active surveillance of avian influenza in LPMs is a major pillar supporting avian influenza control and response. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-019-4079-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-65321772019-05-28 Genetic and biological characteristics of avian influenza virus subtype H1N8 in environments related to live poultry markets in China Zhang, Ye Dong, Jie Bo, Hong Dong, Libo Zou, Shumei Li, Xiyan Shu, Yuelong Wang, Dayan BMC Infect Dis Research Article BACKGROUND: Since 2008, avian influenza surveillance in poultry-related environments has been conducted annually in China. Samples have been collected from environments including live poultry markets, wild bird habitats, slaughterhouses, and poultry farms. Multiple subtypes of avian influenza virus have been identified based on environmental surveillance, and an H1N8 virus was isolated from the drinking water of a live poultry market. METHODS: Virus isolation was performed by inoculating influenza A-positive specimens into embryonated chicken eggs. Next-generation sequencing was used for whole-genome sequencing. A solid-phase binding assay was performed to test the virus receptor binding specificity. Trypsin dependence plaque formation assays and intravenous pathogenicity index tests were used to evaluate virus pathogenicity in vitro and in vivo, respectively. Different cell lines were chosen for comparison of virus replication capacity. RESULTS: According to the phylogenetic trees, the whole gene segments of the virus named A/Environment/Fujian/85144/2014(H1N8) were of Eurasian lineage. The HA, NA, PB1, and M genes showed the highest homology with those of H1N8 or H1N2 subtype viruses isolated from local domestic ducks, while the PB2, PA, NP and NS genes showed high similarity with the genes of H7N9 viruses detected in 2017 and 2018 in the same province. This virus presented an avian receptor binding preference. The plaque formation assay showed that it was a trypsin-dependent virus. The intravenous pathogenicity index (IVPI) in chickens was 0.02. The growth kinetics of the A/Environment/Fujian/85144/2014(H1N8) virus in different cell lines were similar to those of a human-origin virus, A/Brisbane/59/2007(H1N1), but lower than those of the control avian-origin and swine-origin viruses. CONCLUSIONS: The H1N8 virus was identified in avian influenza-related environments in China for the first time and may have served as a gene carrier involved in the evolution of the H7N9 virus in poultry. This work further emphasizes the importance of avian influenza virus surveillance, especially in live poultry markets (LPMs). Active surveillance of avian influenza in LPMs is a major pillar supporting avian influenza control and response. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-019-4079-z) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-22 /pmc/articles/PMC6532177/ /pubmed/31117981 http://dx.doi.org/10.1186/s12879-019-4079-z Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zhang, Ye
Dong, Jie
Bo, Hong
Dong, Libo
Zou, Shumei
Li, Xiyan
Shu, Yuelong
Wang, Dayan
Genetic and biological characteristics of avian influenza virus subtype H1N8 in environments related to live poultry markets in China
title Genetic and biological characteristics of avian influenza virus subtype H1N8 in environments related to live poultry markets in China
title_full Genetic and biological characteristics of avian influenza virus subtype H1N8 in environments related to live poultry markets in China
title_fullStr Genetic and biological characteristics of avian influenza virus subtype H1N8 in environments related to live poultry markets in China
title_full_unstemmed Genetic and biological characteristics of avian influenza virus subtype H1N8 in environments related to live poultry markets in China
title_short Genetic and biological characteristics of avian influenza virus subtype H1N8 in environments related to live poultry markets in China
title_sort genetic and biological characteristics of avian influenza virus subtype h1n8 in environments related to live poultry markets in china
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6532177/
https://www.ncbi.nlm.nih.gov/pubmed/31117981
http://dx.doi.org/10.1186/s12879-019-4079-z
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