Cargando…

Chronic Psychological Stress Disrupted the Composition of the Murine Colonic Microbiota and Accelerated a Murine Model of Inflammatory Bowel Disease

The effect of psychological stress on the gastrointestinal microbiota is widely recognized. Chronic psychological stress may be associated with increased disease activity in inflammatory bowel disease, but the relationships among psychological stress, the gastrointestinal microbiota, and the severit...

Descripción completa

Detalles Bibliográficos
Autores principales: Watanabe, Yohei, Arase, Sohei, Nagaoka, Noriko, Kawai, Mitsuhisa, Matsumoto, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780833/
https://www.ncbi.nlm.nih.gov/pubmed/26950850
http://dx.doi.org/10.1371/journal.pone.0150559
_version_ 1782419819140743168
author Watanabe, Yohei
Arase, Sohei
Nagaoka, Noriko
Kawai, Mitsuhisa
Matsumoto, Satoshi
author_facet Watanabe, Yohei
Arase, Sohei
Nagaoka, Noriko
Kawai, Mitsuhisa
Matsumoto, Satoshi
author_sort Watanabe, Yohei
collection PubMed
description The effect of psychological stress on the gastrointestinal microbiota is widely recognized. Chronic psychological stress may be associated with increased disease activity in inflammatory bowel disease, but the relationships among psychological stress, the gastrointestinal microbiota, and the severity of colitis is not yet fully understood. Here, we examined the impact of 12-week repeated water-avoidance stress on the microbiota of two inbred strains of T cell receptor alpha chain gene knockout mouse (background, BALB/c and C57BL/6) by means of next-generation sequencing of bacterial 16S rRNA genes. In both mouse strains, knockout of the T cell receptor alpha chain gene caused a loss of gastrointestinal microbial diversity and stability. Chronic exposure to repeated water-avoidance stress markedly altered the composition of the colonic microbiota of C57BL/6 mice, but not of BALB/c mice. In C57BL/6 mice, the relative abundance of genus Clostridium, some members of which produce the toxin phospholipase C, was increased, which was weakly positively associated with colitis severity, suggesting that expansion of specific populations of indigenous pathogens may be involved in the exacerbation of colitis. However, we also found that colitis was not exacerbated in mice with a relatively diverse microbiota even if their colonic microbiota contained an expanded phospholipase C-producing Clostridium population. Exposure to chronic stress also altered the concentration of free immunoglobulin A in colonic contents, which may be related to both the loss of bacterial diversity in the colonic microbiota and the severity of the colitis exacerbation. Together, these results suggest that long-term exposure to psychological stress induces dysbiosis in the immunodeficient mouse in a strain-specific manner and also that alteration of microbial diversity, which may be related to an altered pattern of immunoglobulin secretion in the gastrointestinal tract, might play a crucial role in the development of chronic stress-induced colitis.
format Online
Article
Text
id pubmed-4780833
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-47808332016-03-23 Chronic Psychological Stress Disrupted the Composition of the Murine Colonic Microbiota and Accelerated a Murine Model of Inflammatory Bowel Disease Watanabe, Yohei Arase, Sohei Nagaoka, Noriko Kawai, Mitsuhisa Matsumoto, Satoshi PLoS One Research Article The effect of psychological stress on the gastrointestinal microbiota is widely recognized. Chronic psychological stress may be associated with increased disease activity in inflammatory bowel disease, but the relationships among psychological stress, the gastrointestinal microbiota, and the severity of colitis is not yet fully understood. Here, we examined the impact of 12-week repeated water-avoidance stress on the microbiota of two inbred strains of T cell receptor alpha chain gene knockout mouse (background, BALB/c and C57BL/6) by means of next-generation sequencing of bacterial 16S rRNA genes. In both mouse strains, knockout of the T cell receptor alpha chain gene caused a loss of gastrointestinal microbial diversity and stability. Chronic exposure to repeated water-avoidance stress markedly altered the composition of the colonic microbiota of C57BL/6 mice, but not of BALB/c mice. In C57BL/6 mice, the relative abundance of genus Clostridium, some members of which produce the toxin phospholipase C, was increased, which was weakly positively associated with colitis severity, suggesting that expansion of specific populations of indigenous pathogens may be involved in the exacerbation of colitis. However, we also found that colitis was not exacerbated in mice with a relatively diverse microbiota even if their colonic microbiota contained an expanded phospholipase C-producing Clostridium population. Exposure to chronic stress also altered the concentration of free immunoglobulin A in colonic contents, which may be related to both the loss of bacterial diversity in the colonic microbiota and the severity of the colitis exacerbation. Together, these results suggest that long-term exposure to psychological stress induces dysbiosis in the immunodeficient mouse in a strain-specific manner and also that alteration of microbial diversity, which may be related to an altered pattern of immunoglobulin secretion in the gastrointestinal tract, might play a crucial role in the development of chronic stress-induced colitis. Public Library of Science 2016-03-07 /pmc/articles/PMC4780833/ /pubmed/26950850 http://dx.doi.org/10.1371/journal.pone.0150559 Text en © 2016 Watanabe et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Watanabe, Yohei
Arase, Sohei
Nagaoka, Noriko
Kawai, Mitsuhisa
Matsumoto, Satoshi
Chronic Psychological Stress Disrupted the Composition of the Murine Colonic Microbiota and Accelerated a Murine Model of Inflammatory Bowel Disease
title Chronic Psychological Stress Disrupted the Composition of the Murine Colonic Microbiota and Accelerated a Murine Model of Inflammatory Bowel Disease
title_full Chronic Psychological Stress Disrupted the Composition of the Murine Colonic Microbiota and Accelerated a Murine Model of Inflammatory Bowel Disease
title_fullStr Chronic Psychological Stress Disrupted the Composition of the Murine Colonic Microbiota and Accelerated a Murine Model of Inflammatory Bowel Disease
title_full_unstemmed Chronic Psychological Stress Disrupted the Composition of the Murine Colonic Microbiota and Accelerated a Murine Model of Inflammatory Bowel Disease
title_short Chronic Psychological Stress Disrupted the Composition of the Murine Colonic Microbiota and Accelerated a Murine Model of Inflammatory Bowel Disease
title_sort chronic psychological stress disrupted the composition of the murine colonic microbiota and accelerated a murine model of inflammatory bowel disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780833/
https://www.ncbi.nlm.nih.gov/pubmed/26950850
http://dx.doi.org/10.1371/journal.pone.0150559
work_keys_str_mv AT watanabeyohei chronicpsychologicalstressdisruptedthecompositionofthemurinecolonicmicrobiotaandacceleratedamurinemodelofinflammatoryboweldisease
AT arasesohei chronicpsychologicalstressdisruptedthecompositionofthemurinecolonicmicrobiotaandacceleratedamurinemodelofinflammatoryboweldisease
AT nagaokanoriko chronicpsychologicalstressdisruptedthecompositionofthemurinecolonicmicrobiotaandacceleratedamurinemodelofinflammatoryboweldisease
AT kawaimitsuhisa chronicpsychologicalstressdisruptedthecompositionofthemurinecolonicmicrobiotaandacceleratedamurinemodelofinflammatoryboweldisease
AT matsumotosatoshi chronicpsychologicalstressdisruptedthecompositionofthemurinecolonicmicrobiotaandacceleratedamurinemodelofinflammatoryboweldisease