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Assessing potential pathogenicity of novel highly pathogenic avian influenza (H5N6) viruses isolated from Mongolian wild duck feces using a mouse model

Several novel highly pathogenic avian influenza (HPAIVs) A(H5N6) viruses were reported in Mongolia in 2020, some of which included host-specific markers associated with mammalian infection. However, their pathogenicity has not yet been investigated. Here, we isolated and evaluate two novel genotypes...

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Autores principales: Duong, Bao Tuan, Than, Duc Duong, Ankhanbaatar, Ulaankhuu, Gombo-Ochir, Delgerzul, Shura, Gansukh, Tsolmon, Amartuvshin, Pun Mok, Chris Ka, Basan, Ganzorig, Yeo, Seon Ju, Park, Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9154755/
https://www.ncbi.nlm.nih.gov/pubmed/35451353
http://dx.doi.org/10.1080/22221751.2022.2069515
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author Duong, Bao Tuan
Than, Duc Duong
Ankhanbaatar, Ulaankhuu
Gombo-Ochir, Delgerzul
Shura, Gansukh
Tsolmon, Amartuvshin
Pun Mok, Chris Ka
Basan, Ganzorig
Yeo, Seon Ju
Park, Hyun
author_facet Duong, Bao Tuan
Than, Duc Duong
Ankhanbaatar, Ulaankhuu
Gombo-Ochir, Delgerzul
Shura, Gansukh
Tsolmon, Amartuvshin
Pun Mok, Chris Ka
Basan, Ganzorig
Yeo, Seon Ju
Park, Hyun
author_sort Duong, Bao Tuan
collection PubMed
description Several novel highly pathogenic avian influenza (HPAIVs) A(H5N6) viruses were reported in Mongolia in 2020, some of which included host-specific markers associated with mammalian infection. However, their pathogenicity has not yet been investigated. Here, we isolated and evaluate two novel genotypes of A(H5N6) subtype in Mongolia during 2018–2019 (A/wildDuck/MN/H5N6/2018-19). Their evolution pattern and molecular characteristics were evaluated using gene sequencing and their pathogenicity was determined using a mouse model. We also compared their antigenicity with previous H5 Clade 2.3.4.4 human isolates by cross-hemagglutination inhibition (HI). Our data suggests that A/wildDuck/MN/H5N6/2018-19 belongs to clade 2.3.4.4h, and maintains several residues associated with mammal adaptation. In addition, our evaluations revealed that their isolates are less virulent in mice than the previously identified H5 human isolates. However, their antigenicity is distinct from other HPAIVs H5 clade 2.3.4.4, thus supporting their continued evaluation as potential infection risks and the preparation of novel candidate vaccines for their neutralization.
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spelling pubmed-91547552022-06-01 Assessing potential pathogenicity of novel highly pathogenic avian influenza (H5N6) viruses isolated from Mongolian wild duck feces using a mouse model Duong, Bao Tuan Than, Duc Duong Ankhanbaatar, Ulaankhuu Gombo-Ochir, Delgerzul Shura, Gansukh Tsolmon, Amartuvshin Pun Mok, Chris Ka Basan, Ganzorig Yeo, Seon Ju Park, Hyun Emerg Microbes Infect Influenza Infections Several novel highly pathogenic avian influenza (HPAIVs) A(H5N6) viruses were reported in Mongolia in 2020, some of which included host-specific markers associated with mammalian infection. However, their pathogenicity has not yet been investigated. Here, we isolated and evaluate two novel genotypes of A(H5N6) subtype in Mongolia during 2018–2019 (A/wildDuck/MN/H5N6/2018-19). Their evolution pattern and molecular characteristics were evaluated using gene sequencing and their pathogenicity was determined using a mouse model. We also compared their antigenicity with previous H5 Clade 2.3.4.4 human isolates by cross-hemagglutination inhibition (HI). Our data suggests that A/wildDuck/MN/H5N6/2018-19 belongs to clade 2.3.4.4h, and maintains several residues associated with mammal adaptation. In addition, our evaluations revealed that their isolates are less virulent in mice than the previously identified H5 human isolates. However, their antigenicity is distinct from other HPAIVs H5 clade 2.3.4.4, thus supporting their continued evaluation as potential infection risks and the preparation of novel candidate vaccines for their neutralization. Taylor & Francis 2022-05-25 /pmc/articles/PMC9154755/ /pubmed/35451353 http://dx.doi.org/10.1080/22221751.2022.2069515 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Influenza Infections
Duong, Bao Tuan
Than, Duc Duong
Ankhanbaatar, Ulaankhuu
Gombo-Ochir, Delgerzul
Shura, Gansukh
Tsolmon, Amartuvshin
Pun Mok, Chris Ka
Basan, Ganzorig
Yeo, Seon Ju
Park, Hyun
Assessing potential pathogenicity of novel highly pathogenic avian influenza (H5N6) viruses isolated from Mongolian wild duck feces using a mouse model
title Assessing potential pathogenicity of novel highly pathogenic avian influenza (H5N6) viruses isolated from Mongolian wild duck feces using a mouse model
title_full Assessing potential pathogenicity of novel highly pathogenic avian influenza (H5N6) viruses isolated from Mongolian wild duck feces using a mouse model
title_fullStr Assessing potential pathogenicity of novel highly pathogenic avian influenza (H5N6) viruses isolated from Mongolian wild duck feces using a mouse model
title_full_unstemmed Assessing potential pathogenicity of novel highly pathogenic avian influenza (H5N6) viruses isolated from Mongolian wild duck feces using a mouse model
title_short Assessing potential pathogenicity of novel highly pathogenic avian influenza (H5N6) viruses isolated from Mongolian wild duck feces using a mouse model
title_sort assessing potential pathogenicity of novel highly pathogenic avian influenza (h5n6) viruses isolated from mongolian wild duck feces using a mouse model
topic Influenza Infections
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9154755/
https://www.ncbi.nlm.nih.gov/pubmed/35451353
http://dx.doi.org/10.1080/22221751.2022.2069515
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