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In utero human intestine harbors unique metabolome, including bacterial metabolites

Symbiotic microbial colonization through the establishment of the intestinal microbiome is critical to many intestinal functions, including nutrient metabolism, intestinal barrier integrity, and immune regulation. Recent studies suggest that education of intestinal immunity may be ongoing in utero....

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Autores principales: Li, Yujia, Toothaker, Jessica M., Ben-Simon, Shira, Ozeri, Lital, Schweitzer, Ron, McCourt, Blake T., McCourt, Collin C., Werner, Lael, Snapper, Scott B., Shouval, Dror S., Khatib, Soliman, Koren, Omry, Agnihorti, Sameer, Tseng, George, Konnikova, Liza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710283/
https://www.ncbi.nlm.nih.gov/pubmed/33001863
http://dx.doi.org/10.1172/jci.insight.138751
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author Li, Yujia
Toothaker, Jessica M.
Ben-Simon, Shira
Ozeri, Lital
Schweitzer, Ron
McCourt, Blake T.
McCourt, Collin C.
Werner, Lael
Snapper, Scott B.
Shouval, Dror S.
Khatib, Soliman
Koren, Omry
Agnihorti, Sameer
Tseng, George
Konnikova, Liza
author_facet Li, Yujia
Toothaker, Jessica M.
Ben-Simon, Shira
Ozeri, Lital
Schweitzer, Ron
McCourt, Blake T.
McCourt, Collin C.
Werner, Lael
Snapper, Scott B.
Shouval, Dror S.
Khatib, Soliman
Koren, Omry
Agnihorti, Sameer
Tseng, George
Konnikova, Liza
author_sort Li, Yujia
collection PubMed
description Symbiotic microbial colonization through the establishment of the intestinal microbiome is critical to many intestinal functions, including nutrient metabolism, intestinal barrier integrity, and immune regulation. Recent studies suggest that education of intestinal immunity may be ongoing in utero. However, the drivers of this process are unknown. The microbiome and its byproducts are one potential source. Whether a fetal intestinal microbiome exists is controversial, and whether microbially derived metabolites are present in utero is unknown. Here, we aimed to determine whether bacterial DNA and microbially derived metabolites can be detected in second trimester human intestinal samples. Although we were unable to amplify bacterial DNA from fetal intestines, we report a fetal metabolomic intestinal profile with an abundance of bacterially derived and host-derived metabolites commonly produced in response to microbiota. Though we did not directly assess their source and function, we hypothesize that these microbial-associated metabolites either come from the maternal microbiome and are vertically transmitted to the fetus to prime the fetal immune system and prepare the gastrointestinal tract for postnatal microbial encounters or are produced locally by bacteria that were below our detection threshold.
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spelling pubmed-77102832020-12-04 In utero human intestine harbors unique metabolome, including bacterial metabolites Li, Yujia Toothaker, Jessica M. Ben-Simon, Shira Ozeri, Lital Schweitzer, Ron McCourt, Blake T. McCourt, Collin C. Werner, Lael Snapper, Scott B. Shouval, Dror S. Khatib, Soliman Koren, Omry Agnihorti, Sameer Tseng, George Konnikova, Liza JCI Insight Research Article Symbiotic microbial colonization through the establishment of the intestinal microbiome is critical to many intestinal functions, including nutrient metabolism, intestinal barrier integrity, and immune regulation. Recent studies suggest that education of intestinal immunity may be ongoing in utero. However, the drivers of this process are unknown. The microbiome and its byproducts are one potential source. Whether a fetal intestinal microbiome exists is controversial, and whether microbially derived metabolites are present in utero is unknown. Here, we aimed to determine whether bacterial DNA and microbially derived metabolites can be detected in second trimester human intestinal samples. Although we were unable to amplify bacterial DNA from fetal intestines, we report a fetal metabolomic intestinal profile with an abundance of bacterially derived and host-derived metabolites commonly produced in response to microbiota. Though we did not directly assess their source and function, we hypothesize that these microbial-associated metabolites either come from the maternal microbiome and are vertically transmitted to the fetus to prime the fetal immune system and prepare the gastrointestinal tract for postnatal microbial encounters or are produced locally by bacteria that were below our detection threshold. American Society for Clinical Investigation 2020-11-05 /pmc/articles/PMC7710283/ /pubmed/33001863 http://dx.doi.org/10.1172/jci.insight.138751 Text en © 2020 Li et al. http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Li, Yujia
Toothaker, Jessica M.
Ben-Simon, Shira
Ozeri, Lital
Schweitzer, Ron
McCourt, Blake T.
McCourt, Collin C.
Werner, Lael
Snapper, Scott B.
Shouval, Dror S.
Khatib, Soliman
Koren, Omry
Agnihorti, Sameer
Tseng, George
Konnikova, Liza
In utero human intestine harbors unique metabolome, including bacterial metabolites
title In utero human intestine harbors unique metabolome, including bacterial metabolites
title_full In utero human intestine harbors unique metabolome, including bacterial metabolites
title_fullStr In utero human intestine harbors unique metabolome, including bacterial metabolites
title_full_unstemmed In utero human intestine harbors unique metabolome, including bacterial metabolites
title_short In utero human intestine harbors unique metabolome, including bacterial metabolites
title_sort in utero human intestine harbors unique metabolome, including bacterial metabolites
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710283/
https://www.ncbi.nlm.nih.gov/pubmed/33001863
http://dx.doi.org/10.1172/jci.insight.138751
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