» Articles » PMID: 33972766

Fetal Meconium Does Not Have a Detectable Microbiota Before Birth

Overview
Journal Nat Microbiol
Date 2021 May 11
PMID 33972766
Citations 76
Authors
Affiliations
Soon will be listed here.
Abstract

Microbial colonization of the human intestine impacts host metabolism and immunity; however, exactly when colonization occurs is unclear. Although many studies have reported bacterial DNA in first-pass meconium samples, these samples are typically collected hours to days after birth. Here, we investigated whether bacteria could be detected in meconium before birth. Fetal meconium (n = 20) was collected by rectal swab during elective breech caesarean deliveries without labour and before antibiotics and compared to technical and procedural controls (n = 5), first-pass meconium (neonatal meconium; n = 14) and infant stool (n = 25). Unlike first-pass meconium, no microbial signal distinct from negative controls was detected in fetal meconium by 16S ribosomal RNA gene sequencing. Additionally, positive aerobic (n = 10 of 20) and anaerobic (n = 12 of 20) clinical cultures of fetal meconium (13 of 20 samples positive in at least one culture) were identified as likely skin contaminants, most frequently Staphylococcus epidermidis, and not detected by sequencing in most samples (same genera detected by culture and sequencing in 2 of 13 samples with positive culture). We conclude that fetal gut colonization of healthy term infants does not occur before birth and that microbial profiles of neonatal meconium reflect populations acquired during and after birth.

Citing Articles

Gut-X axis.

Lin X, Yu Z, Liu Y, Li C, Hu H, Hu J Imeta. 2025; 4(1):e270.

PMID: 40027477 PMC: 11865426. DOI: 10.1002/imt2.270.


Neonatal microbiome in the multiomics era: development and its impact on long-term health.

Neu J, Stewart C Pediatr Res. 2025; .

PMID: 40021924 DOI: 10.1038/s41390-025-03953-x.


Unveiling early-life microbial colonization profile through characterizing low-biomass maternal-infant microbiomes by 2bRAD-M.

Hou S, Jiang Y, Zhang F, Cheng T, Zhao D, Yao J Front Microbiol. 2025; 16:1521108.

PMID: 39927261 PMC: 11802558. DOI: 10.3389/fmicb.2025.1521108.


Unveiling the neonatal gut microbiota: exploring the influence of delivery mode on early microbial colonization and intervention strategies.

Ma G, Chen Z, Li Z, Xiao X Arch Gynecol Obstet. 2024; 310(6):2853-2861.

PMID: 39589476 DOI: 10.1007/s00404-024-07843-1.


Paternal microbiota impacts offspring: health risks and reproductive insights.

Wang J, Zhang A, Qin S MedComm (2020). 2024; 5(10):e749.

PMID: 39399644 PMC: 11470998. DOI: 10.1002/mco2.749.


References
1.
Sprockett D, Fukami T, Relman D . Role of priority effects in the early-life assembly of the gut microbiota. Nat Rev Gastroenterol Hepatol. 2018; 15(4):197-205. PMC: 6813786. DOI: 10.1038/nrgastro.2017.173. View

2.
Durack J, Kimes N, Lin D, Rauch M, McKean M, McCauley K . Delayed gut microbiota development in high-risk for asthma infants is temporarily modifiable by Lactobacillus supplementation. Nat Commun. 2018; 9(1):707. PMC: 5816017. DOI: 10.1038/s41467-018-03157-4. View

3.
Westrom B, Sureda E, Pierzynowska K, Pierzynowski S, Perez-Cano F . The Immature Gut Barrier and Its Importance in Establishing Immunity in Newborn Mammals. Front Immunol. 2020; 11:1153. PMC: 7296122. DOI: 10.3389/fimmu.2020.01153. View

4.
Axelsson I, Jakobsson I, Lindberg T, Polberger S, Benediktsson B, RAIHA N . Macromolecular absorption in preterm and term infants. Acta Paediatr Scand. 1989; 78(4):532-7. DOI: 10.1111/j.1651-2227.1989.tb17932.x. View

5.
Nanthakumar N, Meng D, Goldstein A, Zhu W, Lu L, Uauy R . The mechanism of excessive intestinal inflammation in necrotizing enterocolitis: an immature innate immune response. PLoS One. 2011; 6(3):e17776. PMC: 3061868. DOI: 10.1371/journal.pone.0017776. View