Viable bacterial colonization is highly limited in the human intestine in utero.

Abstract

Mucosal immunity develops in the human fetal intestine by 11–14 weeks gestation, yet whether viable microbes exist in utero and interact with the intestinal immune system is unknown. Bacterial-like morphology was identified in pockets of human fetal meconium at mid-gestation by scanning electron microscopy (n=4) and a sparse bacterial signal was detected by 16S rRNA sequencing (n=40 of 50) compared to environmental controls (n=87). Eighteen taxa were enriched in fetal meconium with Micrococcaceae (n=9) and Lactobacillus (n=6) the most abundant. Fetal intestines dominated by Micrococcaceae exhibited distinct patterns of T cell composition and epithelial transcription. Fetal Micrococcus luteus, isolated only in the presence of monocytes, grew on placental hormones, remained viable within antigen presenting cells, limited inflammation ex vivo, and possessed genomic features linked with survival in the fetus. Thus, viable bacteria are highly limited in the fetal intestine at mid-gestation, though strains with immunomodulatory capacity are detected in subsets of specimens.