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Rapid evolution of Mexican H7N3 highly pathogenic avian influenza viruses in poultry

Highly pathogenic avian influenza (HPAI) virus subtype H7N3 has been circulating in poultry in Mexico since 2012 and vaccination has been used to control the disease. In this study, eight Mexican H7N3 HPAI viruses from 2015–2017 were isolated and fully sequenced. No evidence of reassortment was dete...

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Autores principales: Youk, Sungsu, Lee, Dong-Hun, Ferreira, Helena L., Afonso, Claudio L., Absalon, Angel E., Swayne, David E., Suarez, David L., Pantin-Jackwood, Mary J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6742402/
https://www.ncbi.nlm.nih.gov/pubmed/31513638
http://dx.doi.org/10.1371/journal.pone.0222457
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author Youk, Sungsu
Lee, Dong-Hun
Ferreira, Helena L.
Afonso, Claudio L.
Absalon, Angel E.
Swayne, David E.
Suarez, David L.
Pantin-Jackwood, Mary J.
author_facet Youk, Sungsu
Lee, Dong-Hun
Ferreira, Helena L.
Afonso, Claudio L.
Absalon, Angel E.
Swayne, David E.
Suarez, David L.
Pantin-Jackwood, Mary J.
author_sort Youk, Sungsu
collection PubMed
description Highly pathogenic avian influenza (HPAI) virus subtype H7N3 has been circulating in poultry in Mexico since 2012 and vaccination has been used to control the disease. In this study, eight Mexican H7N3 HPAI viruses from 2015–2017 were isolated and fully sequenced. No evidence of reassortment was detected with other avian influenza (AI) viruses, but phylogenetic analyses show divergence of all eight gene segments into three genetic clusters by 2015, with 94.94 to 98.78 percent nucleotide homology of the HA genes when compared to the index virus from 2012. The HA protein of viruses from each cluster showed a different number of basic amino acids (n = 5–7) in the cleavage site, and six different patterns at the predicted N-glycosylation sites. Comparison of the sequences of the Mexican lineage H7N3 HPAI viruses and American ancestral wild bird AI viruses to characterize the virus evolutionary dynamics showed that the nucleotide substitution rates in PB2, PB1, PA, HA, NP, and NS genes greatly increased once the virus was introduced into poultry. The global nonsynonymous and synonymous ratios imply strong purifying selection driving the evolution of the virus. Forty-nine positively selected sites out of 171 nonsynonymous mutations were identified in the Mexican H7N3 HPAI viruses, including 7 amino acid changes observed in higher proportion in North American poultry origin AI viruses isolates than in wild bird-origin viruses. Continuous monitoring and molecular characterization of the H7N3 HPAI virus is important for better understanding of the virus evolutionary dynamics and further improving control measures including vaccination.
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spelling pubmed-67424022019-09-20 Rapid evolution of Mexican H7N3 highly pathogenic avian influenza viruses in poultry Youk, Sungsu Lee, Dong-Hun Ferreira, Helena L. Afonso, Claudio L. Absalon, Angel E. Swayne, David E. Suarez, David L. Pantin-Jackwood, Mary J. PLoS One Research Article Highly pathogenic avian influenza (HPAI) virus subtype H7N3 has been circulating in poultry in Mexico since 2012 and vaccination has been used to control the disease. In this study, eight Mexican H7N3 HPAI viruses from 2015–2017 were isolated and fully sequenced. No evidence of reassortment was detected with other avian influenza (AI) viruses, but phylogenetic analyses show divergence of all eight gene segments into three genetic clusters by 2015, with 94.94 to 98.78 percent nucleotide homology of the HA genes when compared to the index virus from 2012. The HA protein of viruses from each cluster showed a different number of basic amino acids (n = 5–7) in the cleavage site, and six different patterns at the predicted N-glycosylation sites. Comparison of the sequences of the Mexican lineage H7N3 HPAI viruses and American ancestral wild bird AI viruses to characterize the virus evolutionary dynamics showed that the nucleotide substitution rates in PB2, PB1, PA, HA, NP, and NS genes greatly increased once the virus was introduced into poultry. The global nonsynonymous and synonymous ratios imply strong purifying selection driving the evolution of the virus. Forty-nine positively selected sites out of 171 nonsynonymous mutations were identified in the Mexican H7N3 HPAI viruses, including 7 amino acid changes observed in higher proportion in North American poultry origin AI viruses isolates than in wild bird-origin viruses. Continuous monitoring and molecular characterization of the H7N3 HPAI virus is important for better understanding of the virus evolutionary dynamics and further improving control measures including vaccination. Public Library of Science 2019-09-12 /pmc/articles/PMC6742402/ /pubmed/31513638 http://dx.doi.org/10.1371/journal.pone.0222457 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Youk, Sungsu
Lee, Dong-Hun
Ferreira, Helena L.
Afonso, Claudio L.
Absalon, Angel E.
Swayne, David E.
Suarez, David L.
Pantin-Jackwood, Mary J.
Rapid evolution of Mexican H7N3 highly pathogenic avian influenza viruses in poultry
title Rapid evolution of Mexican H7N3 highly pathogenic avian influenza viruses in poultry
title_full Rapid evolution of Mexican H7N3 highly pathogenic avian influenza viruses in poultry
title_fullStr Rapid evolution of Mexican H7N3 highly pathogenic avian influenza viruses in poultry
title_full_unstemmed Rapid evolution of Mexican H7N3 highly pathogenic avian influenza viruses in poultry
title_short Rapid evolution of Mexican H7N3 highly pathogenic avian influenza viruses in poultry
title_sort rapid evolution of mexican h7n3 highly pathogenic avian influenza viruses in poultry
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6742402/
https://www.ncbi.nlm.nih.gov/pubmed/31513638
http://dx.doi.org/10.1371/journal.pone.0222457
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