Assessing gut microbiota perturbations during the early phase of infectious diarrhea in Vietnamese children
Diarrheal diseases remain the second most common cause of mortality in young children in developing countries. Efforts have been made to explore the impact of diarrhea on bacterial communities in the human gut, but a thorough understanding has been impeded by inadequate resolution in bacterial ident...
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Veröffentlicht in: | Gut microbes 2018-01, Vol.9 (1), p.38-54 |
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creator | The, Hao Chung Florez de Sessions, Paola Jie, Song Pham Thanh, Duy Thompson, Corinne N Nguyen Ngoc Minh, Chau Chu, Collins Wenhan Tran, Tuan-Anh Thomson, Nicholas R Thwaites, Guy E Rabaa, Maia A Hibberd, Martin Baker, Stephen |
description | Diarrheal diseases remain the second most common cause of mortality in young children in developing countries. Efforts have been made to explore the impact of diarrhea on bacterial communities in the human gut, but a thorough understanding has been impeded by inadequate resolution in bacterial identification and the examination of only few etiological agents. Here, by profiling an extended region of the 16S rRNA gene in the fecal microbiome, we aimed to elucidate the nature of gut microbiome perturbations during the early phase of infectious diarrhea caused by various etiological agents in Vietnamese children. Fecal samples from 145 diarrheal cases with a confirmed infectious etiology before antimicrobial therapy and 54 control subjects were analyzed. We found that the diarrheal fecal microbiota could be robustly categorized into 4 microbial configurations that either generally resembled or were highly divergent from a healthy state. Factors such as age, nutritional status, breastfeeding, and the etiology of the infection were significantly associated with these microbial community structures. We observed a consistent elevation of Fusobacterium mortiferum, Escherichia, and oral microorganisms in all diarrheal fecal microbiome configurations, proposing similar mechanistic interactions, even in the absence of global dysbiosis. We additionally found that Bifidobacterium pseudocatenulatum was significantly depleted during dysenteric diarrhea regardless of the etiological agent, suggesting that further investigations into the use of this species as a dysentery-orientated probiotic therapy are warranted. Our findings contribute to the understanding of the complex influence of infectious diarrhea on gut microbiome and identify new opportunities for therapeutic interventions. |
doi_str_mv | 10.1080/19490976.2017.1361093 |
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Efforts have been made to explore the impact of diarrhea on bacterial communities in the human gut, but a thorough understanding has been impeded by inadequate resolution in bacterial identification and the examination of only few etiological agents. Here, by profiling an extended region of the 16S rRNA gene in the fecal microbiome, we aimed to elucidate the nature of gut microbiome perturbations during the early phase of infectious diarrhea caused by various etiological agents in Vietnamese children. Fecal samples from 145 diarrheal cases with a confirmed infectious etiology before antimicrobial therapy and 54 control subjects were analyzed. We found that the diarrheal fecal microbiota could be robustly categorized into 4 microbial configurations that either generally resembled or were highly divergent from a healthy state. Factors such as age, nutritional status, breastfeeding, and the etiology of the infection were significantly associated with these microbial community structures. We observed a consistent elevation of Fusobacterium mortiferum, Escherichia, and oral microorganisms in all diarrheal fecal microbiome configurations, proposing similar mechanistic interactions, even in the absence of global dysbiosis. We additionally found that Bifidobacterium pseudocatenulatum was significantly depleted during dysenteric diarrhea regardless of the etiological agent, suggesting that further investigations into the use of this species as a dysentery-orientated probiotic therapy are warranted. Our findings contribute to the understanding of the complex influence of infectious diarrhea on gut microbiome and identify new opportunities for therapeutic interventions.</description><identifier>ISSN: 1949-0976</identifier><identifier>EISSN: 1949-0984</identifier><identifier>DOI: 10.1080/19490976.2017.1361093</identifier><identifier>PMID: 28767339</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>Bacteria - classification ; Bacteria - genetics ; Bacterial Physiological Phenomena ; Biodiversity ; Cluster Analysis ; Diarrhea, Infantile - microbiology ; Diarrhea, Infantile - virology ; Dysbiosis - microbiology ; Dysentery - microbiology ; Dysentery - virology ; Feces - microbiology ; Feces - virology ; Female ; Gastrointestinal Microbiome ; Gastrointestinal Tract - microbiology ; Gastrointestinal Tract - virology ; Humans ; Infant ; Male ; Research Paper/Report ; Risk Factors ; RNA, Ribosomal, 16S - genetics ; Vietnam</subject><ispartof>Gut microbes, 2018-01, Vol.9 (1), p.38-54</ispartof><rights>2018 The Author(s). 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Efforts have been made to explore the impact of diarrhea on bacterial communities in the human gut, but a thorough understanding has been impeded by inadequate resolution in bacterial identification and the examination of only few etiological agents. Here, by profiling an extended region of the 16S rRNA gene in the fecal microbiome, we aimed to elucidate the nature of gut microbiome perturbations during the early phase of infectious diarrhea caused by various etiological agents in Vietnamese children. Fecal samples from 145 diarrheal cases with a confirmed infectious etiology before antimicrobial therapy and 54 control subjects were analyzed. We found that the diarrheal fecal microbiota could be robustly categorized into 4 microbial configurations that either generally resembled or were highly divergent from a healthy state. Factors such as age, nutritional status, breastfeeding, and the etiology of the infection were significantly associated with these microbial community structures. We observed a consistent elevation of Fusobacterium mortiferum, Escherichia, and oral microorganisms in all diarrheal fecal microbiome configurations, proposing similar mechanistic interactions, even in the absence of global dysbiosis. We additionally found that Bifidobacterium pseudocatenulatum was significantly depleted during dysenteric diarrhea regardless of the etiological agent, suggesting that further investigations into the use of this species as a dysentery-orientated probiotic therapy are warranted. Our findings contribute to the understanding of the complex influence of infectious diarrhea on gut microbiome and identify new opportunities for therapeutic interventions.</description><subject>Bacteria - classification</subject><subject>Bacteria - genetics</subject><subject>Bacterial Physiological Phenomena</subject><subject>Biodiversity</subject><subject>Cluster Analysis</subject><subject>Diarrhea, Infantile - microbiology</subject><subject>Diarrhea, Infantile - virology</subject><subject>Dysbiosis - microbiology</subject><subject>Dysentery - microbiology</subject><subject>Dysentery - virology</subject><subject>Feces - microbiology</subject><subject>Feces - virology</subject><subject>Female</subject><subject>Gastrointestinal Microbiome</subject><subject>Gastrointestinal Tract - microbiology</subject><subject>Gastrointestinal Tract - virology</subject><subject>Humans</subject><subject>Infant</subject><subject>Male</subject><subject>Research Paper/Report</subject><subject>Risk Factors</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>Vietnam</subject><issn>1949-0976</issn><issn>1949-0984</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkctuHCEQRVEUK7Zsf4IjltnMGAaaxyaSZeUlWcom8RZV08U0ST8mQEfy34eWx6OYTVHFqQvFJeSGsy1nht1yKy2zWm13jOstF4ozK96Qi7W-YdbIt6e9VufkOudfrC4pNVPiHTnfGa20EPaC_L7LGXOO057ul0LH6NPcxrkAPWAqS2qhxHnKtFvSypQeKUIanuihh4x0DjROAX2FlgpFSKlHqDX6GLFMMGKFfB-HLuF0Rc4CDBmvj_GS_Pz86cf9183D9y_f7u8eNl5yXjatCLIR2iCGFv2OgZeqU8F2puaN7iyE1nc-cM7AKADBAFCywJXSuhVeXJKPz7qHpR2x8ziVBIM7pDhCenIzRPf6ZIq9289_XWO5tFxUgQ9HgTT_WTAXN8bscRhgwjqn43bXGKOZWdHmGa3_lnPCcLqGM7d65V68cqtX7uhV7Xv__xtPXS_OiH9orJQI</recordid><startdate>20180102</startdate><enddate>20180102</enddate><creator>The, Hao Chung</creator><creator>Florez de Sessions, Paola</creator><creator>Jie, Song</creator><creator>Pham Thanh, Duy</creator><creator>Thompson, Corinne N</creator><creator>Nguyen Ngoc Minh, Chau</creator><creator>Chu, Collins Wenhan</creator><creator>Tran, Tuan-Anh</creator><creator>Thomson, Nicholas R</creator><creator>Thwaites, Guy E</creator><creator>Rabaa, Maia A</creator><creator>Hibberd, Martin</creator><creator>Baker, Stephen</creator><general>Taylor & Francis</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4028-4074</orcidid></search><sort><creationdate>20180102</creationdate><title>Assessing gut microbiota perturbations during the early phase of infectious diarrhea in Vietnamese children</title><author>The, Hao Chung ; Florez de Sessions, Paola ; Jie, Song ; Pham Thanh, Duy ; Thompson, Corinne N ; Nguyen Ngoc Minh, Chau ; Chu, Collins Wenhan ; Tran, Tuan-Anh ; Thomson, Nicholas R ; Thwaites, Guy E ; Rabaa, Maia A ; Hibberd, Martin ; Baker, Stephen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-b3f45378eefbec20ac46d6f9d8fbe57d9afbcdcf110a86aa30aae40f16677b3c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Bacteria - classification</topic><topic>Bacteria - genetics</topic><topic>Bacterial Physiological Phenomena</topic><topic>Biodiversity</topic><topic>Cluster Analysis</topic><topic>Diarrhea, Infantile - microbiology</topic><topic>Diarrhea, Infantile - virology</topic><topic>Dysbiosis - microbiology</topic><topic>Dysentery - microbiology</topic><topic>Dysentery - virology</topic><topic>Feces - microbiology</topic><topic>Feces - virology</topic><topic>Female</topic><topic>Gastrointestinal Microbiome</topic><topic>Gastrointestinal Tract - microbiology</topic><topic>Gastrointestinal Tract - virology</topic><topic>Humans</topic><topic>Infant</topic><topic>Male</topic><topic>Research Paper/Report</topic><topic>Risk Factors</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>Vietnam</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>The, Hao Chung</creatorcontrib><creatorcontrib>Florez de Sessions, Paola</creatorcontrib><creatorcontrib>Jie, Song</creatorcontrib><creatorcontrib>Pham Thanh, Duy</creatorcontrib><creatorcontrib>Thompson, Corinne N</creatorcontrib><creatorcontrib>Nguyen Ngoc Minh, Chau</creatorcontrib><creatorcontrib>Chu, Collins Wenhan</creatorcontrib><creatorcontrib>Tran, Tuan-Anh</creatorcontrib><creatorcontrib>Thomson, Nicholas R</creatorcontrib><creatorcontrib>Thwaites, Guy E</creatorcontrib><creatorcontrib>Rabaa, Maia A</creatorcontrib><creatorcontrib>Hibberd, Martin</creatorcontrib><creatorcontrib>Baker, Stephen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Gut microbes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>The, Hao Chung</au><au>Florez de Sessions, Paola</au><au>Jie, Song</au><au>Pham Thanh, Duy</au><au>Thompson, Corinne N</au><au>Nguyen Ngoc Minh, Chau</au><au>Chu, Collins Wenhan</au><au>Tran, Tuan-Anh</au><au>Thomson, Nicholas R</au><au>Thwaites, Guy E</au><au>Rabaa, Maia A</au><au>Hibberd, Martin</au><au>Baker, Stephen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assessing gut microbiota perturbations during the early phase of infectious diarrhea in Vietnamese children</atitle><jtitle>Gut microbes</jtitle><addtitle>Gut Microbes</addtitle><date>2018-01-02</date><risdate>2018</risdate><volume>9</volume><issue>1</issue><spage>38</spage><epage>54</epage><pages>38-54</pages><issn>1949-0976</issn><eissn>1949-0984</eissn><abstract>Diarrheal diseases remain the second most common cause of mortality in young children in developing countries. Efforts have been made to explore the impact of diarrhea on bacterial communities in the human gut, but a thorough understanding has been impeded by inadequate resolution in bacterial identification and the examination of only few etiological agents. Here, by profiling an extended region of the 16S rRNA gene in the fecal microbiome, we aimed to elucidate the nature of gut microbiome perturbations during the early phase of infectious diarrhea caused by various etiological agents in Vietnamese children. Fecal samples from 145 diarrheal cases with a confirmed infectious etiology before antimicrobial therapy and 54 control subjects were analyzed. We found that the diarrheal fecal microbiota could be robustly categorized into 4 microbial configurations that either generally resembled or were highly divergent from a healthy state. Factors such as age, nutritional status, breastfeeding, and the etiology of the infection were significantly associated with these microbial community structures. We observed a consistent elevation of Fusobacterium mortiferum, Escherichia, and oral microorganisms in all diarrheal fecal microbiome configurations, proposing similar mechanistic interactions, even in the absence of global dysbiosis. We additionally found that Bifidobacterium pseudocatenulatum was significantly depleted during dysenteric diarrhea regardless of the etiological agent, suggesting that further investigations into the use of this species as a dysentery-orientated probiotic therapy are warranted. Our findings contribute to the understanding of the complex influence of infectious diarrhea on gut microbiome and identify new opportunities for therapeutic interventions.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>28767339</pmid><doi>10.1080/19490976.2017.1361093</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0002-4028-4074</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bacteria - classification Bacteria - genetics Bacterial Physiological Phenomena Biodiversity Cluster Analysis Diarrhea, Infantile - microbiology Diarrhea, Infantile - virology Dysbiosis - microbiology Dysentery - microbiology Dysentery - virology Feces - microbiology Feces - virology Female Gastrointestinal Microbiome Gastrointestinal Tract - microbiology Gastrointestinal Tract - virology Humans Infant Male Research Paper/Report Risk Factors RNA, Ribosomal, 16S - genetics Vietnam |
title | Assessing gut microbiota perturbations during the early phase of infectious diarrhea in Vietnamese children |
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