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Fetal exposure to the maternal microbiota in humans and mice
Noelle Younge, … , Debra Brandon, Patrick C. Seed
Noelle Younge, … , Debra Brandon, Patrick C. Seed
Published September 3, 2019
Citation Information: JCI Insight. 2019;4(19):e127806. https://doi.org/10.1172/jci.insight.127806.
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Research Article Development Microbiology

Fetal exposure to the maternal microbiota in humans and mice

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Abstract

Previous studies have demonstrated the presence of microbial DNA in the fetal environment. However, it remains unclear whether this DNA represents viable bacteria and how it relates to the maternal microbiota across body sites. We studied the microbiota of human and mouse dyads to understand these relationships, localize bacteria in the fetus, and demonstrate bacterial viability. In human preterm and full-term mother-infant dyads at the time of cesarean delivery, the oral cavity and meconium of newborn infants born as early as 24 weeks of gestation contained a microbiota that was predicted to originate from in utero sources, including the placenta. Using operative deliveries of pregnant mice under highly controlled, sterile conditions in the laboratory, composition, visualization, and viability of bacteria in the in utero compartment and fetal intestine were demonstrated by 16S rRNA gene sequencing, fluorescence in situ hybridization, and bacterial culture. The composition and predicted source of the fetal gut microbiota shifted between mid- and late gestation. Cultivatable bacteria in the fetal intestine were found during mid-gestation but not late gestation. Our results demonstrate a dynamic, viable mammalian fetal microbiota during in utero development.

Authors

Noelle Younge, Jessica R. McCann, Julie Ballard, Catherine Plunkett, Suhail Akhtar, Félix Araújo-Pérez, Amy Murtha, Debra Brandon, Patrick C. Seed

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Figure 6

Bacterial strains cultured from the murine fetal intestine, placenta, and uterus.

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Bacterial strains cultured from the murine fetal intestine, placenta, an...
The top gray-and-white bar indicates individual dams and the embryonic day at the time of sampling, followed by the anatomic site from which the bacterial strains were isolated. Colored squares in the heatmap represent the sites with positive cultures. Fewer samples had positive cultures in late gestation. Strains were identified by Sanger sequencing of the 16S rRNA gene (8F/1492R). The accession number for the top match identified by the Basic Local Alignment Search Tool (BLAST) is shown for each isolate (isolates without a match of at least 94% sequence identity were designated as unknown).

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