The meconium microbiota shares more features with the amniotic fluid microbiota than the maternal fecal and vaginal microbiota

Gut Microbes. 2020 Nov 9;12(1):1794266. doi: 10.1080/19490976.2020.1794266.

Abstract

The early-life gut microbiota is associated with potential development of diseases in adulthood. The sterile womb paradigm has been challenged by recent reports that revealed the presence of the meconium, amniotic fluid, and placenta microbiome. This study aimed to explore the maternal origin of the microbiota of neonate meconium by using the PacBio single-molecule real-time circular consensus sequencing technology. Such technology could produce high fidelity reads of full-length 16S rRNA genes, improving the sensitivity and specificity of taxonomic profiling. It also reduced the risk of false positives. This study analyzed the full-length 16S rRNA-based microbiota of maternal samples (amniotic fluid, feces, vaginal fluid, saliva) and first-pass meconium of 39 maternal-neonate pairs. Alpha- and beta-diversity analyses revealed sample type-specific microbiota features. Most sample types were dominated by sequences representing different genera (Lactobacillus and Curvibacter in the amniotic fluid and vaginal fluid microbiota; Bacillus and Escherichia/Shigella in the meconium microbiota; Bacteroides and Faecalibacterium in the maternal fecal microbiota; Streptococcus and Prevotella in the maternal saliva microbiota). Moreover, specific operational taxonomic units (OTUs) were identified in all sample types. Dyad analysis revealed common OTUs between the meconium microbiota and microbiota of multiple maternal samples. The meconium microbiota shared more features with the amniotic fluid microbiota than the maternal fecal and vaginal microbiota. Our results strongly suggested that the meconium microbiota was seeded from multiple maternal body sites, and the amniotic fluid microbiota contributed most to the seeding of the meconium microbiota among the investigated maternal body sites.

Keywords: in utero colonization; Meconium; amniotic fluid; maternal-neonate transmission; sterile womb paradigm; vaginal fluid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amniotic Fluid / microbiology*
  • Delivery, Obstetric
  • Feces / microbiology
  • Female
  • Humans
  • Infant, Newborn
  • Meconium / microbiology*
  • Microbiota*
  • Mothers
  • RNA, Ribosomal, 16S / genetics
  • Saliva / microbiology
  • Vagina / microbiology
  • Young Adult

Substances

  • RNA, Ribosomal, 16S

Grants and funding

This work was supported by the National Natural Science Foundation of China (Grant numbers 31720103911, 31972083, and 31460389), Inner Mongolia Autonomous Region Major Basic Research Open Project (Grant number 201603001), and Inner Mongolia Autonomous Region Major Science and Technology Project (Grant number ZDZX2018018).