Metabolic adaptation in the human gut microbiota during pregnancy and the first year of life
The relationship between the gut microbiome and the human host is dynamic and we may expect adjustments in microbiome function if host physiology changes. Metatranscriptomic approaches should be key in unraveling how such adjustments occur. We employ metatranscriptomic sequencing analyses to study g...
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creator | Gosalbes, María José Compte, Joan Moriano-Gutierrez, Silvia Vallès, Yvonne Jiménez-Hernández, Nuria Pons, Xavier Artacho, Alejandro Francino, M. Pilar |
description | The relationship between the gut microbiome and the human host is dynamic and we may expect adjustments in microbiome function if host physiology changes. Metatranscriptomic approaches should be key in unraveling how such adjustments occur.
We employ metatranscriptomic sequencing analyses to study gene expression in the gut microbiota of infants through their first year of life, and of their mothers days before delivery and one year afterwards.
In infants, hallmarks of aerobic metabolism disappear from the microbial metatranscriptome as development proceeds, while the expression of functions related to carbohydrate transport and metabolism increases and diversifies, approaching that observed in non-pregnant women. Butyrate synthesis enzymes are overexpressed at three months of age, even though most butyrate-producing organisms are still rare. In late pregnancy, the microbiota readjusts the expression of carbohydrate-related functions in a manner consistent with a high availability of glucose.
Our findings suggest that butyrate production may be ensured in the gut of young infants before the typical butyrate synthesizers of the adult gut become abundant. The late pregnancy gut microbiota may be able to access the high levels of blood glucose characteristic of this period. Moreover, late pregnancy gut bacteria may reach stationary phase, which may affect their likelihood of translocating across the intestinal epithelium.
This work was supported by grants CSD2009-00006 (CONSOLIDER Program) and SAF2009-13032-C02-02 from MICINN (Ministry of Science and Innovation, Spain), and by grant SAF2012-31187 from MINECO (Ministry of Economics and Competitiveness, Spain). |
doi_str_mv | 10.1016/j.ebiom.2018.10.071 |
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We employ metatranscriptomic sequencing analyses to study gene expression in the gut microbiota of infants through their first year of life, and of their mothers days before delivery and one year afterwards.
In infants, hallmarks of aerobic metabolism disappear from the microbial metatranscriptome as development proceeds, while the expression of functions related to carbohydrate transport and metabolism increases and diversifies, approaching that observed in non-pregnant women. Butyrate synthesis enzymes are overexpressed at three months of age, even though most butyrate-producing organisms are still rare. In late pregnancy, the microbiota readjusts the expression of carbohydrate-related functions in a manner consistent with a high availability of glucose.
Our findings suggest that butyrate production may be ensured in the gut of young infants before the typical butyrate synthesizers of the adult gut become abundant. The late pregnancy gut microbiota may be able to access the high levels of blood glucose characteristic of this period. Moreover, late pregnancy gut bacteria may reach stationary phase, which may affect their likelihood of translocating across the intestinal epithelium.
This work was supported by grants CSD2009-00006 (CONSOLIDER Program) and SAF2009-13032-C02-02 from MICINN (Ministry of Science and Innovation, Spain), and by grant SAF2012-31187 from MINECO (Ministry of Economics and Competitiveness, Spain).</description><identifier>ISSN: 2352-3964</identifier><identifier>EISSN: 2352-3964</identifier><identifier>DOI: 10.1016/j.ebiom.2018.10.071</identifier><identifier>PMID: 30415891</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adult ; Bacteria - classification ; Bacteria - genetics ; Bacteria - metabolism ; Bacterial Proteins - genetics ; Butyrates - metabolism ; Feces - microbiology ; Female ; Gastrointestinal Microbiome ; Gene Expression Profiling - methods ; Gene Expression Regulation, Bacterial ; Gut ; Humans ; Infant ; Infant, Newborn ; Lipid Metabolism ; Male ; Maternal Age ; Metabolism ; Metatranscriptomics ; Microbiota ; Pregnancy ; Pregnancy Trimester, Third ; Research paper ; Sequence Analysis, RNA - methods</subject><ispartof>EBioMedicine, 2019-01, Vol.39, p.497-509</ispartof><rights>2018 The Authors</rights><rights>Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.</rights><rights>2018 The Authors 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3741-4dbd58fbe83c54cee87c4cad1f856a94e29f83713ccfd9a446fc45fef8ea025a3</citedby><cites>FETCH-LOGICAL-c3741-4dbd58fbe83c54cee87c4cad1f856a94e29f83713ccfd9a446fc45fef8ea025a3</cites><orcidid>0000-0002-4510-5653</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354444/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354444/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30415891$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gosalbes, María José</creatorcontrib><creatorcontrib>Compte, Joan</creatorcontrib><creatorcontrib>Moriano-Gutierrez, Silvia</creatorcontrib><creatorcontrib>Vallès, Yvonne</creatorcontrib><creatorcontrib>Jiménez-Hernández, Nuria</creatorcontrib><creatorcontrib>Pons, Xavier</creatorcontrib><creatorcontrib>Artacho, Alejandro</creatorcontrib><creatorcontrib>Francino, M. Pilar</creatorcontrib><title>Metabolic adaptation in the human gut microbiota during pregnancy and the first year of life</title><title>EBioMedicine</title><addtitle>EBioMedicine</addtitle><description>The relationship between the gut microbiome and the human host is dynamic and we may expect adjustments in microbiome function if host physiology changes. Metatranscriptomic approaches should be key in unraveling how such adjustments occur.
We employ metatranscriptomic sequencing analyses to study gene expression in the gut microbiota of infants through their first year of life, and of their mothers days before delivery and one year afterwards.
In infants, hallmarks of aerobic metabolism disappear from the microbial metatranscriptome as development proceeds, while the expression of functions related to carbohydrate transport and metabolism increases and diversifies, approaching that observed in non-pregnant women. Butyrate synthesis enzymes are overexpressed at three months of age, even though most butyrate-producing organisms are still rare. In late pregnancy, the microbiota readjusts the expression of carbohydrate-related functions in a manner consistent with a high availability of glucose.
Our findings suggest that butyrate production may be ensured in the gut of young infants before the typical butyrate synthesizers of the adult gut become abundant. The late pregnancy gut microbiota may be able to access the high levels of blood glucose characteristic of this period. Moreover, late pregnancy gut bacteria may reach stationary phase, which may affect their likelihood of translocating across the intestinal epithelium.
This work was supported by grants CSD2009-00006 (CONSOLIDER Program) and SAF2009-13032-C02-02 from MICINN (Ministry of Science and Innovation, Spain), and by grant SAF2012-31187 from MINECO (Ministry of Economics and Competitiveness, Spain).</description><subject>Adult</subject><subject>Bacteria - classification</subject><subject>Bacteria - genetics</subject><subject>Bacteria - metabolism</subject><subject>Bacterial Proteins - genetics</subject><subject>Butyrates - metabolism</subject><subject>Feces - microbiology</subject><subject>Female</subject><subject>Gastrointestinal Microbiome</subject><subject>Gene Expression Profiling - methods</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Gut</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Lipid Metabolism</subject><subject>Male</subject><subject>Maternal Age</subject><subject>Metabolism</subject><subject>Metatranscriptomics</subject><subject>Microbiota</subject><subject>Pregnancy</subject><subject>Pregnancy Trimester, Third</subject><subject>Research paper</subject><subject>Sequence Analysis, RNA - methods</subject><issn>2352-3964</issn><issn>2352-3964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UcFqGzEQXUpDE9J8QaHo2IsdaSWttYcWSkjbQEovyS0gZqWRLbMruZI24L-vHKchvVSXEW_evDfMa5oPjC4ZZd3ldomDj9OypUxVZElX7E1z1nLZLnjfibev_qfNRc5bSimTooLqXXPKqWBS9eysefiJBYY4ekPAwq5A8TEQH0jZINnMEwSynguZvEmxGhYgdk4-rMku4TpAMHsCwT6xnU-5kD1CItGR0Tt835w4GDNePNfz5v7b9d3Vj8Xtr-83V19vF4avBFsIO1ip3ICKGykMoloZYcAyp2QHvcC2d4qvGDfG2R6E6JwR0qFTCLSVwM-bL0fd3TxMaA2GkmDUu-QnSHsdwet_O8Fv9Do-6o5LUV8V-PQskOLvGXPRk88GxxECxjnrlvG2larrWaXyI7UeJOeE7sWGUX2IRm_1UzT6EM0BrNHUqY-vN3yZ-RtEJXw-ErDe6dFj0tl4DAatT2iKttH_1-APUFejKw</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Gosalbes, María José</creator><creator>Compte, Joan</creator><creator>Moriano-Gutierrez, Silvia</creator><creator>Vallès, Yvonne</creator><creator>Jiménez-Hernández, Nuria</creator><creator>Pons, Xavier</creator><creator>Artacho, Alejandro</creator><creator>Francino, M. Pilar</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-4510-5653</orcidid></search><sort><creationdate>20190101</creationdate><title>Metabolic adaptation in the human gut microbiota during pregnancy and the first year of life</title><author>Gosalbes, María José ; Compte, Joan ; Moriano-Gutierrez, Silvia ; Vallès, Yvonne ; Jiménez-Hernández, Nuria ; Pons, Xavier ; Artacho, Alejandro ; Francino, M. Pilar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3741-4dbd58fbe83c54cee87c4cad1f856a94e29f83713ccfd9a446fc45fef8ea025a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Bacteria - classification</topic><topic>Bacteria - genetics</topic><topic>Bacteria - metabolism</topic><topic>Bacterial Proteins - genetics</topic><topic>Butyrates - metabolism</topic><topic>Feces - microbiology</topic><topic>Female</topic><topic>Gastrointestinal Microbiome</topic><topic>Gene Expression Profiling - methods</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Gut</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Lipid Metabolism</topic><topic>Male</topic><topic>Maternal Age</topic><topic>Metabolism</topic><topic>Metatranscriptomics</topic><topic>Microbiota</topic><topic>Pregnancy</topic><topic>Pregnancy Trimester, Third</topic><topic>Research paper</topic><topic>Sequence Analysis, RNA - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gosalbes, María José</creatorcontrib><creatorcontrib>Compte, Joan</creatorcontrib><creatorcontrib>Moriano-Gutierrez, Silvia</creatorcontrib><creatorcontrib>Vallès, Yvonne</creatorcontrib><creatorcontrib>Jiménez-Hernández, Nuria</creatorcontrib><creatorcontrib>Pons, Xavier</creatorcontrib><creatorcontrib>Artacho, Alejandro</creatorcontrib><creatorcontrib>Francino, M. Pilar</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>EBioMedicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gosalbes, María José</au><au>Compte, Joan</au><au>Moriano-Gutierrez, Silvia</au><au>Vallès, Yvonne</au><au>Jiménez-Hernández, Nuria</au><au>Pons, Xavier</au><au>Artacho, Alejandro</au><au>Francino, M. Pilar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolic adaptation in the human gut microbiota during pregnancy and the first year of life</atitle><jtitle>EBioMedicine</jtitle><addtitle>EBioMedicine</addtitle><date>2019-01-01</date><risdate>2019</risdate><volume>39</volume><spage>497</spage><epage>509</epage><pages>497-509</pages><issn>2352-3964</issn><eissn>2352-3964</eissn><abstract>The relationship between the gut microbiome and the human host is dynamic and we may expect adjustments in microbiome function if host physiology changes. Metatranscriptomic approaches should be key in unraveling how such adjustments occur.
We employ metatranscriptomic sequencing analyses to study gene expression in the gut microbiota of infants through their first year of life, and of their mothers days before delivery and one year afterwards.
In infants, hallmarks of aerobic metabolism disappear from the microbial metatranscriptome as development proceeds, while the expression of functions related to carbohydrate transport and metabolism increases and diversifies, approaching that observed in non-pregnant women. Butyrate synthesis enzymes are overexpressed at three months of age, even though most butyrate-producing organisms are still rare. In late pregnancy, the microbiota readjusts the expression of carbohydrate-related functions in a manner consistent with a high availability of glucose.
Our findings suggest that butyrate production may be ensured in the gut of young infants before the typical butyrate synthesizers of the adult gut become abundant. The late pregnancy gut microbiota may be able to access the high levels of blood glucose characteristic of this period. Moreover, late pregnancy gut bacteria may reach stationary phase, which may affect their likelihood of translocating across the intestinal epithelium.
This work was supported by grants CSD2009-00006 (CONSOLIDER Program) and SAF2009-13032-C02-02 from MICINN (Ministry of Science and Innovation, Spain), and by grant SAF2012-31187 from MINECO (Ministry of Economics and Competitiveness, Spain).</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30415891</pmid><doi>10.1016/j.ebiom.2018.10.071</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-4510-5653</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Bacteria - classification Bacteria - genetics Bacteria - metabolism Bacterial Proteins - genetics Butyrates - metabolism Feces - microbiology Female Gastrointestinal Microbiome Gene Expression Profiling - methods Gene Expression Regulation, Bacterial Gut Humans Infant Infant, Newborn Lipid Metabolism Male Maternal Age Metabolism Metatranscriptomics Microbiota Pregnancy Pregnancy Trimester, Third Research paper Sequence Analysis, RNA - methods |
title | Metabolic adaptation in the human gut microbiota during pregnancy and the first year of life |
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