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Respiratory Viral Infection Alters the Gut Microbiota by Inducing Inappetence

Respiratory viral infections are extremely common, but their impacts on the composition and function of the gut microbiota are poorly understood. We previously observed a significant change in the gut microbiota after viral lung infection. Here, we show that weight loss during respiratory syncytial...

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Autores principales: Groves, Helen T., Higham, Sophie L., Moffatt, Miriam F., Cox, Michael J., Tregoning, John S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029140/
https://www.ncbi.nlm.nih.gov/pubmed/32071269
http://dx.doi.org/10.1128/mBio.03236-19
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author Groves, Helen T.
Higham, Sophie L.
Moffatt, Miriam F.
Cox, Michael J.
Tregoning, John S.
author_facet Groves, Helen T.
Higham, Sophie L.
Moffatt, Miriam F.
Cox, Michael J.
Tregoning, John S.
author_sort Groves, Helen T.
collection PubMed
description Respiratory viral infections are extremely common, but their impacts on the composition and function of the gut microbiota are poorly understood. We previously observed a significant change in the gut microbiota after viral lung infection. Here, we show that weight loss during respiratory syncytial virus (RSV) or influenza virus infection was due to decreased food consumption, and that the fasting of mice altered gut microbiota composition independently of infection. While the acute phase tumor necrosis factor alpha (TNF-α) response drove early weight loss and inappetence during RSV infection, this was not sufficient to induce changes in the gut microbiota. However, the depletion of CD8(+) cells increased food intake and prevented weight loss, resulting in a reversal of the gut microbiota changes normally observed during RSV infection. Viral infection also led to changes in the fecal gut metabolome, with a significant shift in lipid metabolism. Sphingolipids, polyunsaturated fatty acids (PUFAs), and the short-chain fatty acid (SCFA) valerate were all increased in abundance in the fecal metabolome following RSV infection. Whether this and the impact of infection-induced anorexia on the gut microbiota are part of a protective anti-inflammatory response during respiratory viral infections remains to be determined.
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spelling pubmed-70291402020-02-26 Respiratory Viral Infection Alters the Gut Microbiota by Inducing Inappetence Groves, Helen T. Higham, Sophie L. Moffatt, Miriam F. Cox, Michael J. Tregoning, John S. mBio Research Article Respiratory viral infections are extremely common, but their impacts on the composition and function of the gut microbiota are poorly understood. We previously observed a significant change in the gut microbiota after viral lung infection. Here, we show that weight loss during respiratory syncytial virus (RSV) or influenza virus infection was due to decreased food consumption, and that the fasting of mice altered gut microbiota composition independently of infection. While the acute phase tumor necrosis factor alpha (TNF-α) response drove early weight loss and inappetence during RSV infection, this was not sufficient to induce changes in the gut microbiota. However, the depletion of CD8(+) cells increased food intake and prevented weight loss, resulting in a reversal of the gut microbiota changes normally observed during RSV infection. Viral infection also led to changes in the fecal gut metabolome, with a significant shift in lipid metabolism. Sphingolipids, polyunsaturated fatty acids (PUFAs), and the short-chain fatty acid (SCFA) valerate were all increased in abundance in the fecal metabolome following RSV infection. Whether this and the impact of infection-induced anorexia on the gut microbiota are part of a protective anti-inflammatory response during respiratory viral infections remains to be determined. American Society for Microbiology 2020-02-18 /pmc/articles/PMC7029140/ /pubmed/32071269 http://dx.doi.org/10.1128/mBio.03236-19 Text en Copyright © 2020 Groves et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Groves, Helen T.
Higham, Sophie L.
Moffatt, Miriam F.
Cox, Michael J.
Tregoning, John S.
Respiratory Viral Infection Alters the Gut Microbiota by Inducing Inappetence
title Respiratory Viral Infection Alters the Gut Microbiota by Inducing Inappetence
title_full Respiratory Viral Infection Alters the Gut Microbiota by Inducing Inappetence
title_fullStr Respiratory Viral Infection Alters the Gut Microbiota by Inducing Inappetence
title_full_unstemmed Respiratory Viral Infection Alters the Gut Microbiota by Inducing Inappetence
title_short Respiratory Viral Infection Alters the Gut Microbiota by Inducing Inappetence
title_sort respiratory viral infection alters the gut microbiota by inducing inappetence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029140/
https://www.ncbi.nlm.nih.gov/pubmed/32071269
http://dx.doi.org/10.1128/mBio.03236-19
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