» Articles » PMID: 32012716

Prenatal and Peripartum Exposure to Antibiotics and Cesarean Section Delivery Are Associated with Differences in Diversity and Composition of the Infant Meconium Microbiome

Abstract

The meconium microbiome may provide insight into intrauterine and peripartum exposures and the very earliest intestinal pioneering microbes. Prenatal antibiotics have been associated with later obesity in children, which is thought to be driven by microbiome dependent mechanisms. However, there is little data regarding associations of prenatal or peripartum antibiotic exposure, with or without cesarean section (CS), with the features of the meconium microbiome. In this study, 16S ribosomal RNA gene sequencing was performed on bacterial DNA of meconium samples from 105 infants in a birth cohort study. After multivariable adjustment, delivery mode ( = 0.044), prenatal antibiotic use ( = 0.005) and peripartum antibiotic use ( < 0.001) were associated with beta diversity of the infant meconium microbiome. CS (vs. vaginal delivery) and peripartum antibiotics were also associated with greater alpha diversity of the meconium microbiome (Shannon and Simpson, < 0.05). Meconium from infants born by CS (vs. vaginal delivery) had lower relative abundance of the genus ( < 0.001). Prenatal antibiotic use and peripartum antibiotic use (both in the overall analytic sample and when restricting to vaginally delivered infants) were associated with differential abundance of several bacterial taxa in the meconium. Bacterial taxa in the meconium microbiome were also differentially associated with infant excess weight at 12 months of age, however, sample size was limited for this comparison. In conclusion, prenatal and peripartum antibiotic use along with CS delivery were associated with differences in the diversity and composition of the meconium microbiome. Whether or not these differences in the meconium microbiome portend risk for long-term health outcomes warrants further exploration.

Citing Articles

A critical review of microbiome-derived metabolic functions and translational research in liver diseases.

Ganesan R, Thirumurugan D, Vinayagam S, Kim D, Suk K, Iyer M Front Cell Infect Microbiol. 2025; 15:1488874.

PMID: 40066068 PMC: 11891185. DOI: 10.3389/fcimb.2025.1488874.


More than just a number: the gut microbiota and brain function across the extremes of life.

Nuzum N, Deady C, Kittel-Schneider S, Cryan J, OMahony S, Clarke G Gut Microbes. 2024; 16(1):2418988.

PMID: 39567371 PMC: 11583591. DOI: 10.1080/19490976.2024.2418988.


An evaluation of in utero polycyclic aromatic hydrocarbon exposure on the neonatal meconium microbiome.

Keerthy D, Spratlen M, Wen L, Seeram D, Park H, Calero L Environ Res. 2024; 263(Pt 1):120053.

PMID: 39341532 PMC: 11816390. DOI: 10.1016/j.envres.2024.120053.


Microbiome in Female Reproductive Health: Implications for Fertility and Assisted Reproductive Technologies.

Xiao L, Zuo Z, Zhao F Genomics Proteomics Bioinformatics. 2024; 22(1).

PMID: 38862423 PMC: 11104452. DOI: 10.1093/gpbjnl/qzad005.


Fecal transplant from vaginally seeded infants decreases intraabdominal adiposity in mice.

Namasivayam S, Tilves C, Ding H, Wu S, Domingue J, Ruiz-Bedoya C Gut Microbes. 2024; 16(1):2353394.

PMID: 38743047 PMC: 11095576. DOI: 10.1080/19490976.2024.2353394.


References
1.
Fouhy F, Ross R, Fitzgerald G, Stanton C, Cotter P . Composition of the early intestinal microbiota: knowledge, knowledge gaps and the use of high-throughput sequencing to address these gaps. Gut Microbes. 2012; 3(3):203-20. PMC: 3427213. DOI: 10.4161/gmic.20169. View

2.
Schrag S, Gorwitz R, Fultz-Butts K, Schuchat A . Prevention of perinatal group B streptococcal disease. Revised guidelines from CDC. MMWR Recomm Rep. 2002; 51(RR-11):1-22. View

3.
Wilczynska P, Skarzynska E, Lisowska-Myjak B . Meconium microbiome as a new source of information about long-term health and disease: questions and answers. J Matern Fetal Neonatal Med. 2017; 32(4):681-686. DOI: 10.1080/14767058.2017.1387888. View

4.
Darmasseelane K, Hyde M, Santhakumaran S, Gale C, Modi N . Mode of delivery and offspring body mass index, overweight and obesity in adult life: a systematic review and meta-analysis. PLoS One. 2014; 9(2):e87896. PMC: 3935836. DOI: 10.1371/journal.pone.0087896. View

5.
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