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Symbiotic gut microbes modulate human metabolic phenotypes
Humans have evolved intimate symbiotic relationships with a consortium of gut microbes (microbiome) and individual variations in the microbiome influence host health, may be implicated in disease etiology, and affect drug metabolism, toxicity, and efficacy. However, the molecular basis of these micr...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2008-02, Vol.105 (6), p.2117-2122 |
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container_title | Proceedings of the National Academy of Sciences - PNAS |
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creator | Li, Min Wang, Baohong Zhang, Menghui Rantalainen, Mattias Wang, Shengyue Zhou, Haokui Zhang, Yan Shen, Jian Pang, Xiaoyan Zhang, Meiling Wei, Hua Chen, Yu Lu, Haifeng Zuo, Jian Su, Mingming Qiu, Yunping Jia, Wei Xiao, Chaoni Smith, Leon M Yang, Shengli Holmes, Elaine Tang, Huiru Zhao, Guoping Nicholson, Jeremy K Li, Lanjuan Zhao, Liping |
description | Humans have evolved intimate symbiotic relationships with a consortium of gut microbes (microbiome) and individual variations in the microbiome influence host health, may be implicated in disease etiology, and affect drug metabolism, toxicity, and efficacy. However, the molecular basis of these microbe-host interactions and the roles of individual bacterial species are obscure. We now demonstrate a"transgenomic" approach to link gut microbiome and metabolic phenotype (metabotype) variation. We have used a combination of spectroscopic, microbiomic, and multivariate statistical tools to analyze fecal and urinary samples from seven Chinese individuals (sampled twice) and to model the microbial-host metabolic connectivities. At the species level, we found structural differences in the Chinese family gut microbiomes and those reported for American volunteers, which is consistent with population microbial cometabolic differences reported in epidemiological studies. We also introduce the concept of functional metagenomics, defined as "the characterization of key functional members of the microbiome that most influence host metabolism and hence health." For example, Faecalibacterium prausnitzii population variation is associated with modulation of eight urinary metabolites of diverse structure, indicating that this species is a highly functionally active member of the microbiome, influencing numerous host pathways. Other species were identified showing different and varied metabolic interactions. Our approach for understanding the dynamic basis of host-microbiome symbiosis provides a foundation for the development of functional metagenomics as a probe of systemic effects of drugs and diet that are of relevance to personal and public health care solutions. |
doi_str_mv | 10.1073/pnas.0712038105 |
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However, the molecular basis of these microbe-host interactions and the roles of individual bacterial species are obscure. We now demonstrate a"transgenomic" approach to link gut microbiome and metabolic phenotype (metabotype) variation. We have used a combination of spectroscopic, microbiomic, and multivariate statistical tools to analyze fecal and urinary samples from seven Chinese individuals (sampled twice) and to model the microbial-host metabolic connectivities. At the species level, we found structural differences in the Chinese family gut microbiomes and those reported for American volunteers, which is consistent with population microbial cometabolic differences reported in epidemiological studies. We also introduce the concept of functional metagenomics, defined as "the characterization of key functional members of the microbiome that most influence host metabolism and hence health." For example, Faecalibacterium prausnitzii population variation is associated with modulation of eight urinary metabolites of diverse structure, indicating that this species is a highly functionally active member of the microbiome, influencing numerous host pathways. Other species were identified showing different and varied metabolic interactions. Our approach for understanding the dynamic basis of host-microbiome symbiosis provides a foundation for the development of functional metagenomics as a probe of systemic effects of drugs and diet that are of relevance to personal and public health care solutions.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.0712038105</identifier><identifier>PMID: 18252821</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Bacteria ; Bacteria - classification ; Bacteria - isolation & purification ; Bacteroides ; Biological Sciences ; Biological variation ; Electrophoresis, Polyacrylamide Gel ; Energy metabolism ; Epidemiology ; Faecalibacterium prausnitzii ; Gels ; Genomics ; Genotype & phenotype ; Humans ; Intestines - microbiology ; Lipid metabolism ; Magnetic Resonance Spectroscopy ; Metabolic diseases ; Metabolism ; Metabolites ; Microbiota ; Molecular biology ; Molecular Sequence Data ; Phenotype ; Phenotypes ; Phylogeny ; Symbiosis</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (6), p.2117-2122</ispartof><rights>Copyright 2008 The National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Feb 12, 2008</rights><rights>2008 by The National Academy of Sciences of the USA</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c616t-ef52cdfe59697301da2259bfcf2e16bff81f408249c5ecd1883af70a79d60eab3</citedby><cites>FETCH-LOGICAL-c616t-ef52cdfe59697301da2259bfcf2e16bff81f408249c5ecd1883af70a79d60eab3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/105/6.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/25451423$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/25451423$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18252821$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Min</creatorcontrib><creatorcontrib>Wang, Baohong</creatorcontrib><creatorcontrib>Zhang, Menghui</creatorcontrib><creatorcontrib>Rantalainen, Mattias</creatorcontrib><creatorcontrib>Wang, Shengyue</creatorcontrib><creatorcontrib>Zhou, Haokui</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Shen, Jian</creatorcontrib><creatorcontrib>Pang, Xiaoyan</creatorcontrib><creatorcontrib>Zhang, Meiling</creatorcontrib><creatorcontrib>Wei, Hua</creatorcontrib><creatorcontrib>Chen, Yu</creatorcontrib><creatorcontrib>Lu, Haifeng</creatorcontrib><creatorcontrib>Zuo, Jian</creatorcontrib><creatorcontrib>Su, Mingming</creatorcontrib><creatorcontrib>Qiu, Yunping</creatorcontrib><creatorcontrib>Jia, Wei</creatorcontrib><creatorcontrib>Xiao, Chaoni</creatorcontrib><creatorcontrib>Smith, Leon M</creatorcontrib><creatorcontrib>Yang, Shengli</creatorcontrib><creatorcontrib>Holmes, Elaine</creatorcontrib><creatorcontrib>Tang, Huiru</creatorcontrib><creatorcontrib>Zhao, Guoping</creatorcontrib><creatorcontrib>Nicholson, Jeremy K</creatorcontrib><creatorcontrib>Li, Lanjuan</creatorcontrib><creatorcontrib>Zhao, Liping</creatorcontrib><title>Symbiotic gut microbes modulate human metabolic phenotypes</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Humans have evolved intimate symbiotic relationships with a consortium of gut microbes (microbiome) and individual variations in the microbiome influence host health, may be implicated in disease etiology, and affect drug metabolism, toxicity, and efficacy. However, the molecular basis of these microbe-host interactions and the roles of individual bacterial species are obscure. We now demonstrate a"transgenomic" approach to link gut microbiome and metabolic phenotype (metabotype) variation. We have used a combination of spectroscopic, microbiomic, and multivariate statistical tools to analyze fecal and urinary samples from seven Chinese individuals (sampled twice) and to model the microbial-host metabolic connectivities. At the species level, we found structural differences in the Chinese family gut microbiomes and those reported for American volunteers, which is consistent with population microbial cometabolic differences reported in epidemiological studies. We also introduce the concept of functional metagenomics, defined as "the characterization of key functional members of the microbiome that most influence host metabolism and hence health." For example, Faecalibacterium prausnitzii population variation is associated with modulation of eight urinary metabolites of diverse structure, indicating that this species is a highly functionally active member of the microbiome, influencing numerous host pathways. Other species were identified showing different and varied metabolic interactions. Our approach for understanding the dynamic basis of host-microbiome symbiosis provides a foundation for the development of functional metagenomics as a probe of systemic effects of drugs and diet that are of relevance to personal and public health care solutions.</description><subject>Bacteria</subject><subject>Bacteria - classification</subject><subject>Bacteria - isolation & purification</subject><subject>Bacteroides</subject><subject>Biological Sciences</subject><subject>Biological variation</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Energy metabolism</subject><subject>Epidemiology</subject><subject>Faecalibacterium prausnitzii</subject><subject>Gels</subject><subject>Genomics</subject><subject>Genotype & phenotype</subject><subject>Humans</subject><subject>Intestines - microbiology</subject><subject>Lipid metabolism</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Metabolic diseases</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Microbiota</subject><subject>Molecular biology</subject><subject>Molecular Sequence Data</subject><subject>Phenotype</subject><subject>Phenotypes</subject><subject>Phylogeny</subject><subject>Symbiosis</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp9kUFv1DAQhS0EokvpmRMQcYBT2hknTuwekFAFtFIlDm3PluPYu1klcbAdxP57HO2qWzhwmsP75mnePELeIJwj1MXFNKpwDjVSKDgCe0ZWCALzqhTwnKwAaJ3zkpYn5FUIWwAQjMNLcoKcMsoprsjl3W5oOhc7na3nmA2d9q4xIRtcO_cqmmwzD2rMBhNV4_pETRszuribTHhNXljVB3N2mKfk4dvX-6vr_PbH95urL7e5rrCKubGM6tYaJipRF4CtopSJxmpLDVaNtRxtCZyWQjOjW-S8ULYGVYu2AqOa4pR83vtOczOYVpsxetXLyXeD8jvpVCf_VsZuI9ful6Ss4JzXyeDjwcC7n7MJUQ5d0Kbv1WjcHCQFXqEAnsAP_4BbN_sxhUsMFmX6JEvQxR5KnwrBG_t4CYJcSpFLKfJYStp49zTAkT-08ARYNo92TFaSIi4JPv0XkHbu-2h-x0S-3ZPbEJ1_RCkrGZa0SPr7vW6Vk2rtuyAf7pZwAJwJkc7_AzlSs94</recordid><startdate>20080212</startdate><enddate>20080212</enddate><creator>Li, Min</creator><creator>Wang, Baohong</creator><creator>Zhang, Menghui</creator><creator>Rantalainen, Mattias</creator><creator>Wang, Shengyue</creator><creator>Zhou, Haokui</creator><creator>Zhang, Yan</creator><creator>Shen, Jian</creator><creator>Pang, Xiaoyan</creator><creator>Zhang, Meiling</creator><creator>Wei, Hua</creator><creator>Chen, Yu</creator><creator>Lu, Haifeng</creator><creator>Zuo, Jian</creator><creator>Su, Mingming</creator><creator>Qiu, Yunping</creator><creator>Jia, Wei</creator><creator>Xiao, Chaoni</creator><creator>Smith, Leon M</creator><creator>Yang, Shengli</creator><creator>Holmes, Elaine</creator><creator>Tang, Huiru</creator><creator>Zhao, Guoping</creator><creator>Nicholson, Jeremy K</creator><creator>Li, Lanjuan</creator><creator>Zhao, Liping</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><scope>FBQ</scope><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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7T7</scope><scope>5PM</scope></search><sort><creationdate>20080212</creationdate><title>Symbiotic gut microbes modulate human metabolic phenotypes</title><author>Li, Min ; Wang, Baohong ; Zhang, Menghui ; Rantalainen, Mattias ; Wang, Shengyue ; Zhou, Haokui ; Zhang, Yan ; Shen, Jian ; Pang, Xiaoyan ; Zhang, Meiling ; Wei, Hua ; Chen, Yu ; Lu, Haifeng ; Zuo, Jian ; Su, Mingming ; Qiu, Yunping ; Jia, Wei ; Xiao, Chaoni ; Smith, Leon M ; Yang, Shengli ; Holmes, Elaine ; Tang, Huiru ; Zhao, Guoping ; Nicholson, Jeremy K ; Li, Lanjuan ; Zhao, Liping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c616t-ef52cdfe59697301da2259bfcf2e16bff81f408249c5ecd1883af70a79d60eab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Bacteria</topic><topic>Bacteria - classification</topic><topic>Bacteria - isolation & purification</topic><topic>Bacteroides</topic><topic>Biological Sciences</topic><topic>Biological variation</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Energy metabolism</topic><topic>Epidemiology</topic><topic>Faecalibacterium prausnitzii</topic><topic>Gels</topic><topic>Genomics</topic><topic>Genotype & phenotype</topic><topic>Humans</topic><topic>Intestines - microbiology</topic><topic>Lipid metabolism</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Metabolic diseases</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Microbiota</topic><topic>Molecular biology</topic><topic>Molecular Sequence Data</topic><topic>Phenotype</topic><topic>Phenotypes</topic><topic>Phylogeny</topic><topic>Symbiosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Min</creatorcontrib><creatorcontrib>Wang, Baohong</creatorcontrib><creatorcontrib>Zhang, Menghui</creatorcontrib><creatorcontrib>Rantalainen, Mattias</creatorcontrib><creatorcontrib>Wang, Shengyue</creatorcontrib><creatorcontrib>Zhou, Haokui</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Shen, Jian</creatorcontrib><creatorcontrib>Pang, Xiaoyan</creatorcontrib><creatorcontrib>Zhang, Meiling</creatorcontrib><creatorcontrib>Wei, Hua</creatorcontrib><creatorcontrib>Chen, Yu</creatorcontrib><creatorcontrib>Lu, Haifeng</creatorcontrib><creatorcontrib>Zuo, Jian</creatorcontrib><creatorcontrib>Su, Mingming</creatorcontrib><creatorcontrib>Qiu, Yunping</creatorcontrib><creatorcontrib>Jia, Wei</creatorcontrib><creatorcontrib>Xiao, Chaoni</creatorcontrib><creatorcontrib>Smith, Leon M</creatorcontrib><creatorcontrib>Yang, Shengli</creatorcontrib><creatorcontrib>Holmes, Elaine</creatorcontrib><creatorcontrib>Tang, Huiru</creatorcontrib><creatorcontrib>Zhao, Guoping</creatorcontrib><creatorcontrib>Nicholson, Jeremy K</creatorcontrib><creatorcontrib>Li, Lanjuan</creatorcontrib><creatorcontrib>Zhao, Liping</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Min</au><au>Wang, Baohong</au><au>Zhang, Menghui</au><au>Rantalainen, Mattias</au><au>Wang, Shengyue</au><au>Zhou, Haokui</au><au>Zhang, Yan</au><au>Shen, Jian</au><au>Pang, Xiaoyan</au><au>Zhang, Meiling</au><au>Wei, Hua</au><au>Chen, Yu</au><au>Lu, Haifeng</au><au>Zuo, Jian</au><au>Su, Mingming</au><au>Qiu, Yunping</au><au>Jia, Wei</au><au>Xiao, Chaoni</au><au>Smith, Leon M</au><au>Yang, Shengli</au><au>Holmes, Elaine</au><au>Tang, Huiru</au><au>Zhao, Guoping</au><au>Nicholson, Jeremy K</au><au>Li, Lanjuan</au><au>Zhao, Liping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Symbiotic gut microbes modulate human metabolic phenotypes</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2008-02-12</date><risdate>2008</risdate><volume>105</volume><issue>6</issue><spage>2117</spage><epage>2122</epage><pages>2117-2122</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Humans have evolved intimate symbiotic relationships with a consortium of gut microbes (microbiome) and individual variations in the microbiome influence host health, may be implicated in disease etiology, and affect drug metabolism, toxicity, and efficacy. However, the molecular basis of these microbe-host interactions and the roles of individual bacterial species are obscure. We now demonstrate a"transgenomic" approach to link gut microbiome and metabolic phenotype (metabotype) variation. We have used a combination of spectroscopic, microbiomic, and multivariate statistical tools to analyze fecal and urinary samples from seven Chinese individuals (sampled twice) and to model the microbial-host metabolic connectivities. At the species level, we found structural differences in the Chinese family gut microbiomes and those reported for American volunteers, which is consistent with population microbial cometabolic differences reported in epidemiological studies. We also introduce the concept of functional metagenomics, defined as "the characterization of key functional members of the microbiome that most influence host metabolism and hence health." For example, Faecalibacterium prausnitzii population variation is associated with modulation of eight urinary metabolites of diverse structure, indicating that this species is a highly functionally active member of the microbiome, influencing numerous host pathways. Other species were identified showing different and varied metabolic interactions. Our approach for understanding the dynamic basis of host-microbiome symbiosis provides a foundation for the development of functional metagenomics as a probe of systemic effects of drugs and diet that are of relevance to personal and public health care solutions.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>18252821</pmid><doi>10.1073/pnas.0712038105</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | Open Access: PubMed Central; JSTOR Archival Journals and Primary Sources Collection |
subjects | Bacteria Bacteria - classification Bacteria - isolation & purification Bacteroides Biological Sciences Biological variation Electrophoresis, Polyacrylamide Gel Energy metabolism Epidemiology Faecalibacterium prausnitzii Gels Genomics Genotype & phenotype Humans Intestines - microbiology Lipid metabolism Magnetic Resonance Spectroscopy Metabolic diseases Metabolism Metabolites Microbiota Molecular biology Molecular Sequence Data Phenotype Phenotypes Phylogeny Symbiosis |
title | Symbiotic gut microbes modulate human metabolic phenotypes |
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