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Hypergravity disrupts murine intestinal microbiota

During spaceflight, organisms are subjected to various physical stressors including modification of gravity (G) that, associated with lifestyle, could lead to impaired immunity, intestinal dysbiosis and thus potentially predispose astronauts to illness. Whether space travel affects microbiota homeos...

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Autores principales: Alauzet, Corentine, Cunat, Lisiane, Wack, Maxime, Lozniewski, Alain, Busby, Hélène, Agrinier, Nelly, Cailliez-Grimal, Catherine, Frippiat, Jean-Pol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6599200/
https://www.ncbi.nlm.nih.gov/pubmed/31253829
http://dx.doi.org/10.1038/s41598-019-45153-8
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author Alauzet, Corentine
Cunat, Lisiane
Wack, Maxime
Lozniewski, Alain
Busby, Hélène
Agrinier, Nelly
Cailliez-Grimal, Catherine
Frippiat, Jean-Pol
author_facet Alauzet, Corentine
Cunat, Lisiane
Wack, Maxime
Lozniewski, Alain
Busby, Hélène
Agrinier, Nelly
Cailliez-Grimal, Catherine
Frippiat, Jean-Pol
author_sort Alauzet, Corentine
collection PubMed
description During spaceflight, organisms are subjected to various physical stressors including modification of gravity (G) that, associated with lifestyle, could lead to impaired immunity, intestinal dysbiosis and thus potentially predispose astronauts to illness. Whether space travel affects microbiota homeostasis has not been thoroughly investigated. The aim of this study was to evaluate changes in intestinal microbiota and mucosa in a ground-based murine model consisting in a 21-days confinement of mice in a centrifuge running at 2 or 3G. Results revealed an increased α-diversity and a significant change in intracaecal β-diversity observed only at 3G, with profiles characterized by a decrease of the Firmicutes/Bacteroidetes ratio. Compared to 1G microbiota, 12.1% of the taxa were significantly impacted in 3G microbiota, most of them (78%) being enriched. This study shows a G-level-dependent disruption of intracaecal microbiota, without alteration of mucosal integrity. These first data reinforce those recently obtained with in-flight experimentations or microgravity models, and emphasize the critical need for further studies exploring the impact of spaceflight on intestinal microbiota in order to optimize long-term space travel conditions.
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spelling pubmed-65992002019-07-10 Hypergravity disrupts murine intestinal microbiota Alauzet, Corentine Cunat, Lisiane Wack, Maxime Lozniewski, Alain Busby, Hélène Agrinier, Nelly Cailliez-Grimal, Catherine Frippiat, Jean-Pol Sci Rep Article During spaceflight, organisms are subjected to various physical stressors including modification of gravity (G) that, associated with lifestyle, could lead to impaired immunity, intestinal dysbiosis and thus potentially predispose astronauts to illness. Whether space travel affects microbiota homeostasis has not been thoroughly investigated. The aim of this study was to evaluate changes in intestinal microbiota and mucosa in a ground-based murine model consisting in a 21-days confinement of mice in a centrifuge running at 2 or 3G. Results revealed an increased α-diversity and a significant change in intracaecal β-diversity observed only at 3G, with profiles characterized by a decrease of the Firmicutes/Bacteroidetes ratio. Compared to 1G microbiota, 12.1% of the taxa were significantly impacted in 3G microbiota, most of them (78%) being enriched. This study shows a G-level-dependent disruption of intracaecal microbiota, without alteration of mucosal integrity. These first data reinforce those recently obtained with in-flight experimentations or microgravity models, and emphasize the critical need for further studies exploring the impact of spaceflight on intestinal microbiota in order to optimize long-term space travel conditions. Nature Publishing Group UK 2019-06-28 /pmc/articles/PMC6599200/ /pubmed/31253829 http://dx.doi.org/10.1038/s41598-019-45153-8 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
Alauzet, Corentine
Cunat, Lisiane
Wack, Maxime
Lozniewski, Alain
Busby, Hélène
Agrinier, Nelly
Cailliez-Grimal, Catherine
Frippiat, Jean-Pol
Hypergravity disrupts murine intestinal microbiota
title Hypergravity disrupts murine intestinal microbiota
title_full Hypergravity disrupts murine intestinal microbiota
title_fullStr Hypergravity disrupts murine intestinal microbiota
title_full_unstemmed Hypergravity disrupts murine intestinal microbiota
title_short Hypergravity disrupts murine intestinal microbiota
title_sort hypergravity disrupts murine intestinal microbiota
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6599200/
https://www.ncbi.nlm.nih.gov/pubmed/31253829
http://dx.doi.org/10.1038/s41598-019-45153-8
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