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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
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.
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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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