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Akkermansia muciniphila Improves Host Defense Against Influenza Virus Infection

Influenza virus infection can alter the composition of the gut microbiota, while its pathogenicity can, in turn, be highly influenced by the gut microbiota. However, the details underlying these associations remain to be determined. The H7N9 influenza virus is an emerging zoonotic pathogen which has...

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Autores principales: Hu, Xiaotong, Zhao, Ya, Yang, Yong, Gong, Wenxiao, Sun, Xiaomei, Yang, Li, Zhang, Qiang, Jin, Meilin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884316/
https://www.ncbi.nlm.nih.gov/pubmed/33603716
http://dx.doi.org/10.3389/fmicb.2020.586476
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author Hu, Xiaotong
Zhao, Ya
Yang, Yong
Gong, Wenxiao
Sun, Xiaomei
Yang, Li
Zhang, Qiang
Jin, Meilin
author_facet Hu, Xiaotong
Zhao, Ya
Yang, Yong
Gong, Wenxiao
Sun, Xiaomei
Yang, Li
Zhang, Qiang
Jin, Meilin
author_sort Hu, Xiaotong
collection PubMed
description Influenza virus infection can alter the composition of the gut microbiota, while its pathogenicity can, in turn, be highly influenced by the gut microbiota. However, the details underlying these associations remain to be determined. The H7N9 influenza virus is an emerging zoonotic pathogen which has caused the death of 616 humans and has incurred huge losses in the poultry industry. Here, we investigated the effects of infection with highly pathogenic H7N9 on gut microbiota and determined potential anti-influenza microbes. 16S rRNA sequencing results show that H7N9 infection alters the mouse gut microbiota by promoting the growth of Akkermansia, Ruminococcus 1, and Ruminococcaceae UCG-010, and reducing the abundance of Rikenellaceae RC9 gut group and Lachnoclostridium. Although the abundance of Akkermansia muciniphila is positively related to H7N9 infection, the oral administration of cultures, especially of pasteurized A. muciniphila, can significantly reduce weight loss and mortality caused by H7N9 infection in mice. Furthermore, oral administration of live or pasteurized A. muciniphila significantly reduces pulmonary viral titers and the levels IL-1β and IL-6 but enhances the levels of IFN-β, IFN-γ, and IL-10 in H7N9-infected mice, suggesting that the anti-influenza role of A. muciniphila is due to its anti-inflammatory and immunoregulatory properties. Taken together, we showed that the changes in the gut microbiota are associated with H7N9 infection and demonstrated the anti-influenza role of A. muciniphila, which enriches current knowledge about how specific gut bacterial strains protect against influenza infection and suggests a potential anti-influenza probiotic.
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spelling pubmed-78843162021-02-17 Akkermansia muciniphila Improves Host Defense Against Influenza Virus Infection Hu, Xiaotong Zhao, Ya Yang, Yong Gong, Wenxiao Sun, Xiaomei Yang, Li Zhang, Qiang Jin, Meilin Front Microbiol Microbiology Influenza virus infection can alter the composition of the gut microbiota, while its pathogenicity can, in turn, be highly influenced by the gut microbiota. However, the details underlying these associations remain to be determined. The H7N9 influenza virus is an emerging zoonotic pathogen which has caused the death of 616 humans and has incurred huge losses in the poultry industry. Here, we investigated the effects of infection with highly pathogenic H7N9 on gut microbiota and determined potential anti-influenza microbes. 16S rRNA sequencing results show that H7N9 infection alters the mouse gut microbiota by promoting the growth of Akkermansia, Ruminococcus 1, and Ruminococcaceae UCG-010, and reducing the abundance of Rikenellaceae RC9 gut group and Lachnoclostridium. Although the abundance of Akkermansia muciniphila is positively related to H7N9 infection, the oral administration of cultures, especially of pasteurized A. muciniphila, can significantly reduce weight loss and mortality caused by H7N9 infection in mice. Furthermore, oral administration of live or pasteurized A. muciniphila significantly reduces pulmonary viral titers and the levels IL-1β and IL-6 but enhances the levels of IFN-β, IFN-γ, and IL-10 in H7N9-infected mice, suggesting that the anti-influenza role of A. muciniphila is due to its anti-inflammatory and immunoregulatory properties. Taken together, we showed that the changes in the gut microbiota are associated with H7N9 infection and demonstrated the anti-influenza role of A. muciniphila, which enriches current knowledge about how specific gut bacterial strains protect against influenza infection and suggests a potential anti-influenza probiotic. Frontiers Media S.A. 2021-02-02 /pmc/articles/PMC7884316/ /pubmed/33603716 http://dx.doi.org/10.3389/fmicb.2020.586476 Text en Copyright © 2021 Hu, Zhao, Yang, Gong, Sun, Yang, Zhang and Jin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Hu, Xiaotong
Zhao, Ya
Yang, Yong
Gong, Wenxiao
Sun, Xiaomei
Yang, Li
Zhang, Qiang
Jin, Meilin
Akkermansia muciniphila Improves Host Defense Against Influenza Virus Infection
title Akkermansia muciniphila Improves Host Defense Against Influenza Virus Infection
title_full Akkermansia muciniphila Improves Host Defense Against Influenza Virus Infection
title_fullStr Akkermansia muciniphila Improves Host Defense Against Influenza Virus Infection
title_full_unstemmed Akkermansia muciniphila Improves Host Defense Against Influenza Virus Infection
title_short Akkermansia muciniphila Improves Host Defense Against Influenza Virus Infection
title_sort akkermansia muciniphila improves host defense against influenza virus infection
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884316/
https://www.ncbi.nlm.nih.gov/pubmed/33603716
http://dx.doi.org/10.3389/fmicb.2020.586476
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