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Adenovirus infection is associated with altered gut microbial communities in a non-human primate

Adenovirus (AdV) infections are one of the main causes of diarrhea in young children. Enteric AdVs probably disrupt gut microbial defences, which can result in diarrhea. To understand the role of the gut microbiome in AdV-induced pathologies, we investigated the gut microbiome of a naturally AdV-inf...

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Autores principales: Wasimuddin, Corman, Victor M., Ganzhorn, Jörg U., Rakotondranary, Jacques, Ratovonamana, Yedidya R., Drosten, Christian, Sommer, Simone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746978/
https://www.ncbi.nlm.nih.gov/pubmed/31527752
http://dx.doi.org/10.1038/s41598-019-49829-z
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author Wasimuddin
Corman, Victor M.
Ganzhorn, Jörg U.
Rakotondranary, Jacques
Ratovonamana, Yedidya R.
Drosten, Christian
Sommer, Simone
author_facet Wasimuddin
Corman, Victor M.
Ganzhorn, Jörg U.
Rakotondranary, Jacques
Ratovonamana, Yedidya R.
Drosten, Christian
Sommer, Simone
author_sort Wasimuddin
collection PubMed
description Adenovirus (AdV) infections are one of the main causes of diarrhea in young children. Enteric AdVs probably disrupt gut microbial defences, which can result in diarrhea. To understand the role of the gut microbiome in AdV-induced pathologies, we investigated the gut microbiome of a naturally AdV-infected non-human primate species, the Malagasy mouse lemur (Microcebus griseorufus), which represents an important model in understanding the evolution of diseases. We observed that AdV infection is associated with disruption of the gut microbial community composition. In AdV+ lemurs, several commensal taxa essential for a healthy gut microbiome decreased, whereas genera containing potential pathogens, such as Neisseria, increased in abundance. Microbial co-occurrence networks revealed a loss of important microbial community interactions in AdV+ lemurs and an overrepresentation of Prevotellaceae. The observation of enteric virus-associated loss of commensal bacteria and associated shifts towards pathobionts may represent the missing link for a better understanding of AdV-induced effects in humans, and also for their potential as drivers of co-infections, an area of research that has been largely neglected so far.
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spelling pubmed-67469782019-09-27 Adenovirus infection is associated with altered gut microbial communities in a non-human primate Wasimuddin Corman, Victor M. Ganzhorn, Jörg U. Rakotondranary, Jacques Ratovonamana, Yedidya R. Drosten, Christian Sommer, Simone Sci Rep Article Adenovirus (AdV) infections are one of the main causes of diarrhea in young children. Enteric AdVs probably disrupt gut microbial defences, which can result in diarrhea. To understand the role of the gut microbiome in AdV-induced pathologies, we investigated the gut microbiome of a naturally AdV-infected non-human primate species, the Malagasy mouse lemur (Microcebus griseorufus), which represents an important model in understanding the evolution of diseases. We observed that AdV infection is associated with disruption of the gut microbial community composition. In AdV+ lemurs, several commensal taxa essential for a healthy gut microbiome decreased, whereas genera containing potential pathogens, such as Neisseria, increased in abundance. Microbial co-occurrence networks revealed a loss of important microbial community interactions in AdV+ lemurs and an overrepresentation of Prevotellaceae. The observation of enteric virus-associated loss of commensal bacteria and associated shifts towards pathobionts may represent the missing link for a better understanding of AdV-induced effects in humans, and also for their potential as drivers of co-infections, an area of research that has been largely neglected so far. Nature Publishing Group UK 2019-09-16 /pmc/articles/PMC6746978/ /pubmed/31527752 http://dx.doi.org/10.1038/s41598-019-49829-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wasimuddin
Corman, Victor M.
Ganzhorn, Jörg U.
Rakotondranary, Jacques
Ratovonamana, Yedidya R.
Drosten, Christian
Sommer, Simone
Adenovirus infection is associated with altered gut microbial communities in a non-human primate
title Adenovirus infection is associated with altered gut microbial communities in a non-human primate
title_full Adenovirus infection is associated with altered gut microbial communities in a non-human primate
title_fullStr Adenovirus infection is associated with altered gut microbial communities in a non-human primate
title_full_unstemmed Adenovirus infection is associated with altered gut microbial communities in a non-human primate
title_short Adenovirus infection is associated with altered gut microbial communities in a non-human primate
title_sort adenovirus infection is associated with altered gut microbial communities in a non-human primate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746978/
https://www.ncbi.nlm.nih.gov/pubmed/31527752
http://dx.doi.org/10.1038/s41598-019-49829-z
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