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Temporospatial shifts in the human gut microbiome and metabolome after gastric bypass surgery
Although the etiology of obesity is not well-understood, genetic, environmental, and microbiome elements are recognized as contributors to this rising pandemic. It is well documented that Roux-en-Y gastric bypass (RYGB) surgery drastically alters the fecal microbiome, but data are sparse on temporal...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070067/ https://www.ncbi.nlm.nih.gov/pubmed/32170068 http://dx.doi.org/10.1038/s41522-020-0122-5 |
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author | Ilhan, Zehra Esra DiBaise, John K. Dautel, Sydney E. Isern, Nancy G. Kim, Young-Mo Hoyt, David W. Schepmoes, Athena A. Brewer, Heather M. Weitz, Karl K. Metz, Thomas O. Crowell, Michael D. Kang, Dae-Wook Rittmann, Bruce E. Krajmalnik-Brown, Rosa |
author_facet | Ilhan, Zehra Esra DiBaise, John K. Dautel, Sydney E. Isern, Nancy G. Kim, Young-Mo Hoyt, David W. Schepmoes, Athena A. Brewer, Heather M. Weitz, Karl K. Metz, Thomas O. Crowell, Michael D. Kang, Dae-Wook Rittmann, Bruce E. Krajmalnik-Brown, Rosa |
author_sort | Ilhan, Zehra Esra |
collection | PubMed |
description | Although the etiology of obesity is not well-understood, genetic, environmental, and microbiome elements are recognized as contributors to this rising pandemic. It is well documented that Roux-en-Y gastric bypass (RYGB) surgery drastically alters the fecal microbiome, but data are sparse on temporal and spatial microbiome and metabolome changes, especially in human populations. We characterized the structure and function (through metabolites) of the microbial communities in the gut lumen and structure of microbial communities on mucosal surfaces in nine morbidly obese individuals before, 6 months, and 12 months after RYGB surgery. Moreover, using a comprehensive multi-omic approach, we compared this longitudinal cohort to a previously studied cross-sectional cohort (n = 24). In addition to the expected weight reduction and improvement in obesity-related comorbidities after RYGB surgery, we observed that the impact of surgery was much greater on fecal communities in comparison to mucosal ones. The changes in the fecal microbiome were linked to increased concentrations of branched-chain fatty acids and an overall decrease in secondary bile acid concentrations. The microbiome and metabolome data sets for this longitudinal cohort strengthen our understanding of the persistent impact of RYGB on the gut microbiome and its metabolism. Our findings highlight the importance of changes in mucosal and fecal microbiomes after RYGB surgery. The spatial modifications in the microbiome after RYGB surgery corresponded to persistent changes in fecal fermentation and bile acid metabolism, both of which are associated with improved metabolic outcomes. |
format | Online Article Text |
id | pubmed-7070067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70700672020-03-19 Temporospatial shifts in the human gut microbiome and metabolome after gastric bypass surgery Ilhan, Zehra Esra DiBaise, John K. Dautel, Sydney E. Isern, Nancy G. Kim, Young-Mo Hoyt, David W. Schepmoes, Athena A. Brewer, Heather M. Weitz, Karl K. Metz, Thomas O. Crowell, Michael D. Kang, Dae-Wook Rittmann, Bruce E. Krajmalnik-Brown, Rosa NPJ Biofilms Microbiomes Article Although the etiology of obesity is not well-understood, genetic, environmental, and microbiome elements are recognized as contributors to this rising pandemic. It is well documented that Roux-en-Y gastric bypass (RYGB) surgery drastically alters the fecal microbiome, but data are sparse on temporal and spatial microbiome and metabolome changes, especially in human populations. We characterized the structure and function (through metabolites) of the microbial communities in the gut lumen and structure of microbial communities on mucosal surfaces in nine morbidly obese individuals before, 6 months, and 12 months after RYGB surgery. Moreover, using a comprehensive multi-omic approach, we compared this longitudinal cohort to a previously studied cross-sectional cohort (n = 24). In addition to the expected weight reduction and improvement in obesity-related comorbidities after RYGB surgery, we observed that the impact of surgery was much greater on fecal communities in comparison to mucosal ones. The changes in the fecal microbiome were linked to increased concentrations of branched-chain fatty acids and an overall decrease in secondary bile acid concentrations. The microbiome and metabolome data sets for this longitudinal cohort strengthen our understanding of the persistent impact of RYGB on the gut microbiome and its metabolism. Our findings highlight the importance of changes in mucosal and fecal microbiomes after RYGB surgery. The spatial modifications in the microbiome after RYGB surgery corresponded to persistent changes in fecal fermentation and bile acid metabolism, both of which are associated with improved metabolic outcomes. Nature Publishing Group UK 2020-03-13 /pmc/articles/PMC7070067/ /pubmed/32170068 http://dx.doi.org/10.1038/s41522-020-0122-5 Text en © The Author(s) 2020 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 Ilhan, Zehra Esra DiBaise, John K. Dautel, Sydney E. Isern, Nancy G. Kim, Young-Mo Hoyt, David W. Schepmoes, Athena A. Brewer, Heather M. Weitz, Karl K. Metz, Thomas O. Crowell, Michael D. Kang, Dae-Wook Rittmann, Bruce E. Krajmalnik-Brown, Rosa Temporospatial shifts in the human gut microbiome and metabolome after gastric bypass surgery |
title | Temporospatial shifts in the human gut microbiome and metabolome after gastric bypass surgery |
title_full | Temporospatial shifts in the human gut microbiome and metabolome after gastric bypass surgery |
title_fullStr | Temporospatial shifts in the human gut microbiome and metabolome after gastric bypass surgery |
title_full_unstemmed | Temporospatial shifts in the human gut microbiome and metabolome after gastric bypass surgery |
title_short | Temporospatial shifts in the human gut microbiome and metabolome after gastric bypass surgery |
title_sort | temporospatial shifts in the human gut microbiome and metabolome after gastric bypass surgery |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070067/ https://www.ncbi.nlm.nih.gov/pubmed/32170068 http://dx.doi.org/10.1038/s41522-020-0122-5 |
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