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Reshaping of bacterial molecular hydrogen metabolism contributes to the outgrowth of commensal E. coli during gut inflammation
The composition of gut-associated microbial communities changes during intestinal inflammation, including an expansion of Enterobacteriaceae populations. The mechanisms underlying microbiota changes during inflammation are incompletely understood. Here, we analyzed previously published metagenomic d...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177889/ https://www.ncbi.nlm.nih.gov/pubmed/34085924 http://dx.doi.org/10.7554/eLife.58609 |
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author | Hughes, Elizabeth R Winter, Maria G Alves da Silva, Laice Muramatsu, Matthew K Jimenez, Angel G Gillis, Caroline C Spiga, Luisella Chanin, Rachael B Santos, Renato L Zhu, Wenhan Winter, Sebastian E |
author_facet | Hughes, Elizabeth R Winter, Maria G Alves da Silva, Laice Muramatsu, Matthew K Jimenez, Angel G Gillis, Caroline C Spiga, Luisella Chanin, Rachael B Santos, Renato L Zhu, Wenhan Winter, Sebastian E |
author_sort | Hughes, Elizabeth R |
collection | PubMed |
description | The composition of gut-associated microbial communities changes during intestinal inflammation, including an expansion of Enterobacteriaceae populations. The mechanisms underlying microbiota changes during inflammation are incompletely understood. Here, we analyzed previously published metagenomic datasets with a focus on microbial hydrogen metabolism. The bacterial genomes in the inflamed murine gut and in patients with inflammatory bowel disease contained more genes encoding predicted hydrogen-utilizing hydrogenases compared to communities found under non-inflamed conditions. To validate these findings, we investigated hydrogen metabolism of Escherichia coli, a representative Enterobacteriaceae, in mouse models of colitis. E. coli mutants lacking hydrogenase-1 and hydrogenase-2 displayed decreased fitness during colonization of the inflamed cecum and colon. Utilization of molecular hydrogen was in part dependent on respiration of inflammation-derived electron acceptors. This work highlights the contribution of hydrogenases to alterations of the gut microbiota in the context of non-infectious colitis. |
format | Online Article Text |
id | pubmed-8177889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-81778892021-06-07 Reshaping of bacterial molecular hydrogen metabolism contributes to the outgrowth of commensal E. coli during gut inflammation Hughes, Elizabeth R Winter, Maria G Alves da Silva, Laice Muramatsu, Matthew K Jimenez, Angel G Gillis, Caroline C Spiga, Luisella Chanin, Rachael B Santos, Renato L Zhu, Wenhan Winter, Sebastian E eLife Immunology and Inflammation The composition of gut-associated microbial communities changes during intestinal inflammation, including an expansion of Enterobacteriaceae populations. The mechanisms underlying microbiota changes during inflammation are incompletely understood. Here, we analyzed previously published metagenomic datasets with a focus on microbial hydrogen metabolism. The bacterial genomes in the inflamed murine gut and in patients with inflammatory bowel disease contained more genes encoding predicted hydrogen-utilizing hydrogenases compared to communities found under non-inflamed conditions. To validate these findings, we investigated hydrogen metabolism of Escherichia coli, a representative Enterobacteriaceae, in mouse models of colitis. E. coli mutants lacking hydrogenase-1 and hydrogenase-2 displayed decreased fitness during colonization of the inflamed cecum and colon. Utilization of molecular hydrogen was in part dependent on respiration of inflammation-derived electron acceptors. This work highlights the contribution of hydrogenases to alterations of the gut microbiota in the context of non-infectious colitis. eLife Sciences Publications, Ltd 2021-06-04 /pmc/articles/PMC8177889/ /pubmed/34085924 http://dx.doi.org/10.7554/eLife.58609 Text en © 2021, Hughes et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Immunology and Inflammation Hughes, Elizabeth R Winter, Maria G Alves da Silva, Laice Muramatsu, Matthew K Jimenez, Angel G Gillis, Caroline C Spiga, Luisella Chanin, Rachael B Santos, Renato L Zhu, Wenhan Winter, Sebastian E Reshaping of bacterial molecular hydrogen metabolism contributes to the outgrowth of commensal E. coli during gut inflammation |
title | Reshaping of bacterial molecular hydrogen metabolism contributes to the outgrowth of commensal E. coli during gut inflammation |
title_full | Reshaping of bacterial molecular hydrogen metabolism contributes to the outgrowth of commensal E. coli during gut inflammation |
title_fullStr | Reshaping of bacterial molecular hydrogen metabolism contributes to the outgrowth of commensal E. coli during gut inflammation |
title_full_unstemmed | Reshaping of bacterial molecular hydrogen metabolism contributes to the outgrowth of commensal E. coli during gut inflammation |
title_short | Reshaping of bacterial molecular hydrogen metabolism contributes to the outgrowth of commensal E. coli during gut inflammation |
title_sort | reshaping of bacterial molecular hydrogen metabolism contributes to the outgrowth of commensal e. coli during gut inflammation |
topic | Immunology and Inflammation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177889/ https://www.ncbi.nlm.nih.gov/pubmed/34085924 http://dx.doi.org/10.7554/eLife.58609 |
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