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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...
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Published in: | PloS one 2016-03, Vol.11 (3), p.e0150559-e0150559 |
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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. |
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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.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0150559</identifier><identifier>PMID: 26950850</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Analysis ; Animal models ; Animals ; Avoidance ; Avoidance Learning ; Bacteria ; Biology and Life Sciences ; Care and treatment ; Chains ; Chronic exposure ; Clostridium ; Clostridium - metabolism ; Clostridium - physiology ; Clostridium perfringens ; Colitis ; Colon - microbiology ; Colorectal cancer ; Computer and Information Sciences ; Cytokines ; Diabetes ; Diagnosis ; Disease Models, Animal ; Dysbacteriosis ; Exposure ; Gastrointestinal tract ; Gene Knockout Techniques ; Gene sequencing ; Immunodeficiency ; Immunoglobulin A ; Immunoglobulin A - metabolism ; Immunoglobulins ; Inbreeding ; Inflammation ; Inflammatory bowel disease ; Inflammatory bowel diseases ; Inflammatory Bowel Diseases - genetics ; Inflammatory Bowel Diseases - immunology ; Inflammatory Bowel Diseases - microbiology ; Inflammatory Bowel Diseases - psychology ; Intestine ; Medicine and Health Sciences ; Mice ; Microbiota ; Microbiota (Symbiotic organisms) ; Microorganisms ; Phospholipase ; Phospholipase C ; Physiological aspects ; Psychological stress ; Receptors, Antigen, T-Cell, alpha-beta - deficiency ; Receptors, Antigen, T-Cell, alpha-beta - genetics ; Relative abundance ; Research and Analysis Methods ; Risk factors ; Rodents ; rRNA 16S ; Social Sciences ; Strains (organisms) ; Stress (Psychology) ; Stress concentration ; Stress, Psychological ; Studies ; T cell receptors ; T-cell receptor ; Toxins ; Type C Phospholipases - biosynthesis ; Weight control</subject><ispartof>PloS one, 2016-03, Vol.11 (3), p.e0150559-e0150559</ispartof><rights>COPYRIGHT 2016 Public Library of Science</rights><rights>2016 Watanabe et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2016 Watanabe et al 2016 Watanabe et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-bc410266cb93f76c0e7d5030c70f19291758d393e0ead4d23800a33418c306593</citedby><cites>FETCH-LOGICAL-c692t-bc410266cb93f76c0e7d5030c70f19291758d393e0ead4d23800a33418c306593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1771230419/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1771230419?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26950850$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Chamaillard, Mathias</contributor><creatorcontrib>Watanabe, Yohei</creatorcontrib><creatorcontrib>Arase, Sohei</creatorcontrib><creatorcontrib>Nagaoka, Noriko</creatorcontrib><creatorcontrib>Kawai, Mitsuhisa</creatorcontrib><creatorcontrib>Matsumoto, Satoshi</creatorcontrib><title>Chronic Psychological Stress Disrupted the Composition of the Murine Colonic Microbiota and Accelerated a Murine Model of Inflammatory Bowel Disease</title><title>PloS one</title><addtitle>PLoS One</addtitle><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.</description><subject>Analysis</subject><subject>Animal models</subject><subject>Animals</subject><subject>Avoidance</subject><subject>Avoidance Learning</subject><subject>Bacteria</subject><subject>Biology and Life Sciences</subject><subject>Care and treatment</subject><subject>Chains</subject><subject>Chronic exposure</subject><subject>Clostridium</subject><subject>Clostridium - metabolism</subject><subject>Clostridium - physiology</subject><subject>Clostridium perfringens</subject><subject>Colitis</subject><subject>Colon - microbiology</subject><subject>Colorectal cancer</subject><subject>Computer and Information Sciences</subject><subject>Cytokines</subject><subject>Diabetes</subject><subject>Diagnosis</subject><subject>Disease Models, Animal</subject><subject>Dysbacteriosis</subject><subject>Exposure</subject><subject>Gastrointestinal tract</subject><subject>Gene Knockout Techniques</subject><subject>Gene sequencing</subject><subject>Immunodeficiency</subject><subject>Immunoglobulin A</subject><subject>Immunoglobulin A - metabolism</subject><subject>Immunoglobulins</subject><subject>Inbreeding</subject><subject>Inflammation</subject><subject>Inflammatory bowel disease</subject><subject>Inflammatory bowel diseases</subject><subject>Inflammatory Bowel Diseases - genetics</subject><subject>Inflammatory Bowel Diseases - immunology</subject><subject>Inflammatory Bowel Diseases - microbiology</subject><subject>Inflammatory Bowel Diseases - psychology</subject><subject>Intestine</subject><subject>Medicine and Health Sciences</subject><subject>Mice</subject><subject>Microbiota</subject><subject>Microbiota (Symbiotic organisms)</subject><subject>Microorganisms</subject><subject>Phospholipase</subject><subject>Phospholipase C</subject><subject>Physiological aspects</subject><subject>Psychological stress</subject><subject>Receptors, Antigen, T-Cell, alpha-beta - deficiency</subject><subject>Receptors, Antigen, T-Cell, alpha-beta - genetics</subject><subject>Relative abundance</subject><subject>Research and Analysis Methods</subject><subject>Risk factors</subject><subject>Rodents</subject><subject>rRNA 16S</subject><subject>Social Sciences</subject><subject>Strains (organisms)</subject><subject>Stress (Psychology)</subject><subject>Stress concentration</subject><subject>Stress, Psychological</subject><subject>Studies</subject><subject>T cell receptors</subject><subject>T-cell receptor</subject><subject>Toxins</subject><subject>Type C Phospholipases - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Watanabe, Yohei</au><au>Arase, Sohei</au><au>Nagaoka, Noriko</au><au>Kawai, Mitsuhisa</au><au>Matsumoto, Satoshi</au><au>Chamaillard, Mathias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chronic Psychological Stress Disrupted the Composition of the Murine Colonic Microbiota and Accelerated a Murine Model of Inflammatory Bowel Disease</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2016-03-07</date><risdate>2016</risdate><volume>11</volume><issue>3</issue><spage>e0150559</spage><epage>e0150559</epage><pages>e0150559-e0150559</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26950850</pmid><doi>10.1371/journal.pone.0150559</doi><oa>free_for_read</oa></addata></record> |
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recordid | cdi_plos_journals_1771230419 |
source | Publicly Available Content Database; PubMed |
subjects | Analysis Animal models Animals Avoidance Avoidance Learning Bacteria Biology and Life Sciences Care and treatment Chains Chronic exposure Clostridium Clostridium - metabolism Clostridium - physiology Clostridium perfringens Colitis Colon - microbiology Colorectal cancer Computer and Information Sciences Cytokines Diabetes Diagnosis Disease Models, Animal Dysbacteriosis Exposure Gastrointestinal tract Gene Knockout Techniques Gene sequencing Immunodeficiency Immunoglobulin A Immunoglobulin A - metabolism Immunoglobulins Inbreeding Inflammation Inflammatory bowel disease Inflammatory bowel diseases Inflammatory Bowel Diseases - genetics Inflammatory Bowel Diseases - immunology Inflammatory Bowel Diseases - microbiology Inflammatory Bowel Diseases - psychology Intestine Medicine and Health Sciences Mice Microbiota Microbiota (Symbiotic organisms) Microorganisms Phospholipase Phospholipase C Physiological aspects Psychological stress Receptors, Antigen, T-Cell, alpha-beta - deficiency Receptors, Antigen, T-Cell, alpha-beta - genetics Relative abundance Research and Analysis Methods Risk factors Rodents rRNA 16S Social Sciences Strains (organisms) Stress (Psychology) Stress concentration Stress, Psychological Studies T cell receptors T-cell receptor Toxins Type C Phospholipases - biosynthesis Weight control |
title | Chronic Psychological Stress Disrupted the Composition of the Murine Colonic Microbiota and Accelerated a Murine Model of Inflammatory Bowel Disease |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T15%3A43%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Chronic%20Psychological%20Stress%20Disrupted%20the%20Composition%20of%20the%20Murine%20Colonic%20Microbiota%20and%20Accelerated%20a%20Murine%20Model%20of%20Inflammatory%20Bowel%20Disease&rft.jtitle=PloS%20one&rft.au=Watanabe,%20Yohei&rft.date=2016-03-07&rft.volume=11&rft.issue=3&rft.spage=e0150559&rft.epage=e0150559&rft.pages=e0150559-e0150559&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0150559&rft_dat=%3Cgale_plos_%3EA445462354%3C/gale_plos_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c692t-bc410266cb93f76c0e7d5030c70f19291758d393e0ead4d23800a33418c306593%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1771230419&rft_id=info:pmid/26950850&rft_galeid=A445462354&rfr_iscdi=true |