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...

Full description

Bibliographic Details
Main Authors: Toshifumi Osaka, Eri Moriyama, Shunichi Arai, Yasuhiro Date, Junji Yagi, Jun Kikuchi, Satoshi Tsuneda
Format: Article
Language:English
Published: MDPI AG 2017-12-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/9/12/1329
id doaj-a19db81bb35a48e9a10446e19dd273b0
record_format Article
spelling doaj-a19db81bb35a48e9a10446e19dd273b02020-11-24T20:54:28ZengMDPI AGNutrients2072-66432017-12-01912132910.3390/nu9121329nu9121329Meta-Analysis of Fecal Microbiota and Metabolites in Experimental Colitic Mice during the Inflammatory and Healing PhasesToshifumi Osaka0Eri Moriyama1Shunichi Arai2Yasuhiro Date3Junji Yagi4Jun Kikuchi5Satoshi Tsuneda6Department of Microbiology and Immunology, Tokyo Women’s Medical University, 8-1, Kawada-cho, Shinjuku-ku, Tokyo 162-8666, JapanDepartment of Life Science and Medical Bioscience, Waseda University, 2-2 Wakamatsu-cho, Shinjuku-ku, Tokyo 162-8480, JapanDepartment of Life Science and Medical Bioscience, Waseda University, 2-2 Wakamatsu-cho, Shinjuku-ku, Tokyo 162-8480, JapanRIKEN Center for Sustainable Resource Science, 1-7-22 Suehirocho, Tsurumi-ku, Yokohama, Kanagawa 230-0045, JapanDepartment of Microbiology and Immunology, Tokyo Women’s Medical University, 8-1, Kawada-cho, Shinjuku-ku, Tokyo 162-8666, JapanRIKEN Center for Sustainable Resource Science, 1-7-22 Suehirocho, Tsurumi-ku, Yokohama, Kanagawa 230-0045, JapanDepartment of Life Science and Medical Bioscience, Waseda University, 2-2 Wakamatsu-cho, Shinjuku-ku, Tokyo 162-8480, JapanThe 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 (1H-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, 1H-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.https://www.mdpi.com/2072-6643/9/12/1329gut microbiotadysbiosisinflammatory bowel diseasemetabolomemeta 16S rRNA analysis1H-NMR analysisexperimental colitic miceLactobacillus
collection DOAJ
language English
format Article
sources DOAJ
author Toshifumi Osaka
Eri Moriyama
Shunichi Arai
Yasuhiro Date
Junji Yagi
Jun Kikuchi
Satoshi Tsuneda
spellingShingle Toshifumi Osaka
Eri Moriyama
Shunichi Arai
Yasuhiro Date
Junji Yagi
Jun Kikuchi
Satoshi Tsuneda
Meta-Analysis of Fecal Microbiota and Metabolites in Experimental Colitic Mice during the Inflammatory and Healing Phases
Nutrients
gut microbiota
dysbiosis
inflammatory bowel disease
metabolome
meta 16S rRNA analysis
1H-NMR analysis
experimental colitic mice
Lactobacillus
author_facet Toshifumi Osaka
Eri Moriyama
Shunichi Arai
Yasuhiro Date
Junji Yagi
Jun Kikuchi
Satoshi Tsuneda
author_sort Toshifumi Osaka
title 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_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_sort meta-analysis of fecal microbiota and metabolites in experimental colitic mice during the inflammatory and healing phases
publisher MDPI AG
series Nutrients
issn 2072-6643
publishDate 2017-12-01
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 (1H-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, 1H-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.
topic gut microbiota
dysbiosis
inflammatory bowel disease
metabolome
meta 16S rRNA analysis
1H-NMR analysis
experimental colitic mice
Lactobacillus
url https://www.mdpi.com/2072-6643/9/12/1329
work_keys_str_mv AT toshifumiosaka metaanalysisoffecalmicrobiotaandmetabolitesinexperimentalcoliticmiceduringtheinflammatoryandhealingphases
AT erimoriyama metaanalysisoffecalmicrobiotaandmetabolitesinexperimentalcoliticmiceduringtheinflammatoryandhealingphases
AT shunichiarai metaanalysisoffecalmicrobiotaandmetabolitesinexperimentalcoliticmiceduringtheinflammatoryandhealingphases
AT yasuhirodate metaanalysisoffecalmicrobiotaandmetabolitesinexperimentalcoliticmiceduringtheinflammatoryandhealingphases
AT junjiyagi metaanalysisoffecalmicrobiotaandmetabolitesinexperimentalcoliticmiceduringtheinflammatoryandhealingphases
AT junkikuchi metaanalysisoffecalmicrobiotaandmetabolitesinexperimentalcoliticmiceduringtheinflammatoryandhealingphases
AT satoshitsuneda metaanalysisoffecalmicrobiotaandmetabolitesinexperimentalcoliticmiceduringtheinflammatoryandhealingphases
_version_ 1716794420877066240