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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Veröffentlicht in:EBioMedicine 2019-01, Vol.39, p.497-509
Hauptverfasser: Gosalbes, María José, Compte, Joan, Moriano-Gutierrez, Silvia, Vallès, Yvonne, Jiménez-Hernández, Nuria, Pons, Xavier, Artacho, Alejandro, Francino, M. Pilar
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container_start_page 497
container_title EBioMedicine
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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).
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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. 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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. 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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. 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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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