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Human gut microbiome and metabolite dynamics under simulated microgravity
The Artificial Gravity Bed Rest – European Space Agency (AGBRESA) study was the first joint bed rest study by ESA, DLR, and NASA that examined the effect of simulated weightlessness on the human body and assessed the potential benefits of artificial gravity as a countermeasure in an analog of long-d...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10524775/ https://www.ncbi.nlm.nih.gov/pubmed/37749878 http://dx.doi.org/10.1080/19490976.2023.2259033 |
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author | Ramos-Nascimento, Ana Grenga, Lucia Haange, Sven-Bastiaan Himmelmann, Alexandra Arndt, Franca Sabine Ly, Yen-Tran Miotello, Guylaine Pible, Olivier Jehmlich, Nico Engelmann, Beatrice von Bergen, Martin Mulder, Edwin Frings-Meuthen, Petra Hellweg, Christine Elisabeth Jordan, Jens Rolle-Kampczyk, Ulrike Armengaud, Jean Moeller, Ralf |
author_facet | Ramos-Nascimento, Ana Grenga, Lucia Haange, Sven-Bastiaan Himmelmann, Alexandra Arndt, Franca Sabine Ly, Yen-Tran Miotello, Guylaine Pible, Olivier Jehmlich, Nico Engelmann, Beatrice von Bergen, Martin Mulder, Edwin Frings-Meuthen, Petra Hellweg, Christine Elisabeth Jordan, Jens Rolle-Kampczyk, Ulrike Armengaud, Jean Moeller, Ralf |
author_sort | Ramos-Nascimento, Ana |
collection | PubMed |
description | The Artificial Gravity Bed Rest – European Space Agency (AGBRESA) study was the first joint bed rest study by ESA, DLR, and NASA that examined the effect of simulated weightlessness on the human body and assessed the potential benefits of artificial gravity as a countermeasure in an analog of long-duration spaceflight. In this study, we investigated the impact of simulated microgravity on the gut microbiome of 12 participants during a 60-day head-down tilt bed rest at the :envihab facilities. Over 60 days of simulated microgravity resulted in a mild change in the gut microbiome, with distinct microbial patterns and pathway expression in the feces of the countermeasure group compared to the microgravity simulation-only group. Additionally, we found that the countermeasure protocols selectively increased the abundance of beneficial short-chain fatty acids in the gut, such as acetate, butyrate, and propionate. Some physiological signatures also included the modulation of taxa reported to be either beneficial or opportunistic, indicating a mild adaptation in the microbiome network balance. Our results suggest that monitoring the gut microbial catalog along with pathway clustering and metabolite profiling is an informative synergistic strategy to determine health disturbances and the outcome of countermeasure protocols for future space missions. |
format | Online Article Text |
id | pubmed-10524775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-105247752023-09-28 Human gut microbiome and metabolite dynamics under simulated microgravity Ramos-Nascimento, Ana Grenga, Lucia Haange, Sven-Bastiaan Himmelmann, Alexandra Arndt, Franca Sabine Ly, Yen-Tran Miotello, Guylaine Pible, Olivier Jehmlich, Nico Engelmann, Beatrice von Bergen, Martin Mulder, Edwin Frings-Meuthen, Petra Hellweg, Christine Elisabeth Jordan, Jens Rolle-Kampczyk, Ulrike Armengaud, Jean Moeller, Ralf Gut Microbes Research Paper The Artificial Gravity Bed Rest – European Space Agency (AGBRESA) study was the first joint bed rest study by ESA, DLR, and NASA that examined the effect of simulated weightlessness on the human body and assessed the potential benefits of artificial gravity as a countermeasure in an analog of long-duration spaceflight. In this study, we investigated the impact of simulated microgravity on the gut microbiome of 12 participants during a 60-day head-down tilt bed rest at the :envihab facilities. Over 60 days of simulated microgravity resulted in a mild change in the gut microbiome, with distinct microbial patterns and pathway expression in the feces of the countermeasure group compared to the microgravity simulation-only group. Additionally, we found that the countermeasure protocols selectively increased the abundance of beneficial short-chain fatty acids in the gut, such as acetate, butyrate, and propionate. Some physiological signatures also included the modulation of taxa reported to be either beneficial or opportunistic, indicating a mild adaptation in the microbiome network balance. Our results suggest that monitoring the gut microbial catalog along with pathway clustering and metabolite profiling is an informative synergistic strategy to determine health disturbances and the outcome of countermeasure protocols for future space missions. Taylor & Francis 2023-09-25 /pmc/articles/PMC10524775/ /pubmed/37749878 http://dx.doi.org/10.1080/19490976.2023.2259033 Text en © 2023 erman Aerospace Center. Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Research Paper Ramos-Nascimento, Ana Grenga, Lucia Haange, Sven-Bastiaan Himmelmann, Alexandra Arndt, Franca Sabine Ly, Yen-Tran Miotello, Guylaine Pible, Olivier Jehmlich, Nico Engelmann, Beatrice von Bergen, Martin Mulder, Edwin Frings-Meuthen, Petra Hellweg, Christine Elisabeth Jordan, Jens Rolle-Kampczyk, Ulrike Armengaud, Jean Moeller, Ralf Human gut microbiome and metabolite dynamics under simulated microgravity |
title | Human gut microbiome and metabolite dynamics under simulated microgravity |
title_full | Human gut microbiome and metabolite dynamics under simulated microgravity |
title_fullStr | Human gut microbiome and metabolite dynamics under simulated microgravity |
title_full_unstemmed | Human gut microbiome and metabolite dynamics under simulated microgravity |
title_short | Human gut microbiome and metabolite dynamics under simulated microgravity |
title_sort | human gut microbiome and metabolite dynamics under simulated microgravity |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10524775/ https://www.ncbi.nlm.nih.gov/pubmed/37749878 http://dx.doi.org/10.1080/19490976.2023.2259033 |
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