In utero human intestine harbors unique metabolome, including bacterial metabolites

Yujia Li, Jessica M. Toothaker, Shira Ben-Simon, Lital Ozeri, Ron Schweitzer, Blake T. McCourt, Collin C. McCourt, Lael Werner, Scott B. Snapper, Dror S. Shouval, Soliman Khatib, Omry Koren, Sameer Agnihorti, George Tseng, Liza Konnikova

Research output: Contribution to journalArticlepeer-review

58 Scopus citations

Abstract

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.

Original languageEnglish
Article numbere138751
JournalJCI insight
Volume5
Issue number21
DOIs
StatePublished - 5 Nov 2020

Bibliographical note

Publisher Copyright:
Copyright: © 2020, Li et al. This is an open access article published under the terms of the Creative Commons Attribution 4.0 International License.

Funding

This project used the UPMC Tissue and Research Pathology/Pitt Biospecimen core which is supported in part by award P30CA047904 for fetal samples. We also thank the pediatric surgeons for helping with the collection and the Yimlamai group with the processing of the infant samples. Further, we acknowledge that all the samples were analyzed by Metabolon for the metabolomic profiling.

FundersFunder number
National Institute of Allergy and Infectious DiseasesT32AI089443
Université Pierre et Marie CurieP30CA047904

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