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Syntrophy via Interspecies H(2) Transfer between Christensenella and Methanobrevibacter Underlies Their Global Cooccurrence in the Human Gut
Across human populations, 16S rRNA gene-based surveys of gut microbiomes have revealed that the bacterial family Christensenellaceae and the archaeal family Methanobacteriaceae cooccur and are enriched in individuals with a lean, compared to an obese, body mass index (BMI). Whether these association...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002349/ https://www.ncbi.nlm.nih.gov/pubmed/32019803 http://dx.doi.org/10.1128/mBio.03235-19 |
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author | Ruaud, Albane Esquivel-Elizondo, Sofia de la Cuesta-Zuluaga, Jacobo Waters, Jillian L. Angenent, Largus T. Youngblut, Nicholas D. Ley, Ruth E. |
author_facet | Ruaud, Albane Esquivel-Elizondo, Sofia de la Cuesta-Zuluaga, Jacobo Waters, Jillian L. Angenent, Largus T. Youngblut, Nicholas D. Ley, Ruth E. |
author_sort | Ruaud, Albane |
collection | PubMed |
description | Across human populations, 16S rRNA gene-based surveys of gut microbiomes have revealed that the bacterial family Christensenellaceae and the archaeal family Methanobacteriaceae cooccur and are enriched in individuals with a lean, compared to an obese, body mass index (BMI). Whether these association patterns reflect interactions between metabolic partners, as well as whether these associations play a role in the lean host phenotype with which they associate, remains to be ascertained. Here, we validated previously reported cooccurrence patterns of the two families and their association with a lean BMI with a meta-analysis of 1,821 metagenomes derived from 10 independent studies. Furthermore, we report positive associations at the genus and species levels between Christensenella spp. and Methanobrevibacter smithii, the most abundant methanogen of the human gut. By coculturing three Christensenella spp. with M. smithii, we show that Christensenella spp. efficiently support the metabolism of M. smithii via H(2) production far better than Bacteroides thetaiotaomicron does. Christensenella minuta forms flocs colonized by M. smithii even when H(2) is in excess. In culture with C. minuta, H(2) consumption by M. smithii shifts the metabolic output of C. minuta’s fermentation toward acetate rather than butyrate. Together, these results indicate that the widespread cooccurrence of these microorganisms is underpinned by both physical and metabolic interactions. Their combined metabolic activity may provide insights into their association with a lean host BMI. |
format | Online Article Text |
id | pubmed-7002349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-70023492020-02-11 Syntrophy via Interspecies H(2) Transfer between Christensenella and Methanobrevibacter Underlies Their Global Cooccurrence in the Human Gut Ruaud, Albane Esquivel-Elizondo, Sofia de la Cuesta-Zuluaga, Jacobo Waters, Jillian L. Angenent, Largus T. Youngblut, Nicholas D. Ley, Ruth E. mBio Research Article Across human populations, 16S rRNA gene-based surveys of gut microbiomes have revealed that the bacterial family Christensenellaceae and the archaeal family Methanobacteriaceae cooccur and are enriched in individuals with a lean, compared to an obese, body mass index (BMI). Whether these association patterns reflect interactions between metabolic partners, as well as whether these associations play a role in the lean host phenotype with which they associate, remains to be ascertained. Here, we validated previously reported cooccurrence patterns of the two families and their association with a lean BMI with a meta-analysis of 1,821 metagenomes derived from 10 independent studies. Furthermore, we report positive associations at the genus and species levels between Christensenella spp. and Methanobrevibacter smithii, the most abundant methanogen of the human gut. By coculturing three Christensenella spp. with M. smithii, we show that Christensenella spp. efficiently support the metabolism of M. smithii via H(2) production far better than Bacteroides thetaiotaomicron does. Christensenella minuta forms flocs colonized by M. smithii even when H(2) is in excess. In culture with C. minuta, H(2) consumption by M. smithii shifts the metabolic output of C. minuta’s fermentation toward acetate rather than butyrate. Together, these results indicate that the widespread cooccurrence of these microorganisms is underpinned by both physical and metabolic interactions. Their combined metabolic activity may provide insights into their association with a lean host BMI. American Society for Microbiology 2020-02-04 /pmc/articles/PMC7002349/ /pubmed/32019803 http://dx.doi.org/10.1128/mBio.03235-19 Text en Copyright © 2020 Ruaud 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 Ruaud, Albane Esquivel-Elizondo, Sofia de la Cuesta-Zuluaga, Jacobo Waters, Jillian L. Angenent, Largus T. Youngblut, Nicholas D. Ley, Ruth E. Syntrophy via Interspecies H(2) Transfer between Christensenella and Methanobrevibacter Underlies Their Global Cooccurrence in the Human Gut |
title | Syntrophy via Interspecies H(2) Transfer between Christensenella and Methanobrevibacter Underlies Their Global Cooccurrence in the Human Gut |
title_full | Syntrophy via Interspecies H(2) Transfer between Christensenella and Methanobrevibacter Underlies Their Global Cooccurrence in the Human Gut |
title_fullStr | Syntrophy via Interspecies H(2) Transfer between Christensenella and Methanobrevibacter Underlies Their Global Cooccurrence in the Human Gut |
title_full_unstemmed | Syntrophy via Interspecies H(2) Transfer between Christensenella and Methanobrevibacter Underlies Their Global Cooccurrence in the Human Gut |
title_short | Syntrophy via Interspecies H(2) Transfer between Christensenella and Methanobrevibacter Underlies Their Global Cooccurrence in the Human Gut |
title_sort | syntrophy via interspecies h(2) transfer between christensenella and methanobrevibacter underlies their global cooccurrence in the human gut |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002349/ https://www.ncbi.nlm.nih.gov/pubmed/32019803 http://dx.doi.org/10.1128/mBio.03235-19 |
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