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Meta-Analysis of Fecal Microbiota and Metabolites in Experimental Colitic Mice during the Inflammatory and Healing Phases

The imbalance of gut microbiota is known to be associated with inflammatory bowel disease, but it remains unknown whether dysbiosis is a cause or consequence of chronic gut inflammation. In order to investigate the effects of gut inflammation on microbiota and metabolome, the sequential changes in g...

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Autores principales: Osaka, Toshifumi, Moriyama, Eri, Arai, Shunichi, Date, Yasuhiro, Yagi, Junji, Kikuchi, Jun, Tsuneda, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748779/
https://www.ncbi.nlm.nih.gov/pubmed/29211010
http://dx.doi.org/10.3390/nu9121329
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author Osaka, Toshifumi
Moriyama, Eri
Arai, Shunichi
Date, Yasuhiro
Yagi, Junji
Kikuchi, Jun
Tsuneda, Satoshi
author_facet Osaka, Toshifumi
Moriyama, Eri
Arai, Shunichi
Date, Yasuhiro
Yagi, Junji
Kikuchi, Jun
Tsuneda, Satoshi
author_sort Osaka, Toshifumi
collection PubMed
description The imbalance of gut microbiota is known to be associated with inflammatory bowel disease, but it remains unknown whether dysbiosis is a cause or consequence of chronic gut inflammation. In order to investigate the effects of gut inflammation on microbiota and metabolome, the sequential changes in gut microbiota and metabolites from the onset of colitis to the recovery in dextran sulfate sodium-induced colitic mice were characterized by using meta 16S rRNA sequencing and proton nuclear magnetic resonance ((1)H-NMR) analysis. Mice in the colitis progression phase showed the transient expansions of two bacterial families including Bacteroidaceae and Enterobacteriaceae and the depletion of major gut commensal bacteria belonging to the uncultured Bacteroidales family S24-7, Rikenellaceae, Lachnospiraceae, and Ruminococcaceae. After the initiation of the recovery, commensal Lactobacillus members promptly predominated in gut while other normally abundant bacteria excluding the Erysipelotrichaceae remained diminished. Furthermore, (1)H-NMR analysis revealed characteristic fluctuations in fecal levels of organic acids (lactate and succinate) associated with the disease states. In conclusion, acute intestinal inflammation is a perturbation factor of gut microbiota but alters the intestinal environments suitable for Lactobacillus members.
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spelling pubmed-57487792018-01-07 Meta-Analysis of Fecal Microbiota and Metabolites in Experimental Colitic Mice during the Inflammatory and Healing Phases Osaka, Toshifumi Moriyama, Eri Arai, Shunichi Date, Yasuhiro Yagi, Junji Kikuchi, Jun Tsuneda, Satoshi Nutrients Article The imbalance of gut microbiota is known to be associated with inflammatory bowel disease, but it remains unknown whether dysbiosis is a cause or consequence of chronic gut inflammation. In order to investigate the effects of gut inflammation on microbiota and metabolome, the sequential changes in gut microbiota and metabolites from the onset of colitis to the recovery in dextran sulfate sodium-induced colitic mice were characterized by using meta 16S rRNA sequencing and proton nuclear magnetic resonance ((1)H-NMR) analysis. Mice in the colitis progression phase showed the transient expansions of two bacterial families including Bacteroidaceae and Enterobacteriaceae and the depletion of major gut commensal bacteria belonging to the uncultured Bacteroidales family S24-7, Rikenellaceae, Lachnospiraceae, and Ruminococcaceae. After the initiation of the recovery, commensal Lactobacillus members promptly predominated in gut while other normally abundant bacteria excluding the Erysipelotrichaceae remained diminished. Furthermore, (1)H-NMR analysis revealed characteristic fluctuations in fecal levels of organic acids (lactate and succinate) associated with the disease states. In conclusion, acute intestinal inflammation is a perturbation factor of gut microbiota but alters the intestinal environments suitable for Lactobacillus members. MDPI 2017-12-06 /pmc/articles/PMC5748779/ /pubmed/29211010 http://dx.doi.org/10.3390/nu9121329 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Osaka, Toshifumi
Moriyama, Eri
Arai, Shunichi
Date, Yasuhiro
Yagi, Junji
Kikuchi, Jun
Tsuneda, Satoshi
Meta-Analysis of Fecal Microbiota and Metabolites in Experimental Colitic Mice during the Inflammatory and Healing Phases
title Meta-Analysis of Fecal Microbiota and Metabolites in Experimental Colitic Mice during the Inflammatory and Healing Phases
title_full Meta-Analysis of Fecal Microbiota and Metabolites in Experimental Colitic Mice during the Inflammatory and Healing Phases
title_fullStr Meta-Analysis of Fecal Microbiota and Metabolites in Experimental Colitic Mice during the Inflammatory and Healing Phases
title_full_unstemmed Meta-Analysis of Fecal Microbiota and Metabolites in Experimental Colitic Mice during the Inflammatory and Healing Phases
title_short Meta-Analysis of Fecal Microbiota and Metabolites in Experimental Colitic Mice during the Inflammatory and Healing Phases
title_sort meta-analysis of fecal microbiota and metabolites in experimental colitic mice during the inflammatory and healing phases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748779/
https://www.ncbi.nlm.nih.gov/pubmed/29211010
http://dx.doi.org/10.3390/nu9121329
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