Maternal colonization and early-onset neonatal bacterial sepsis in the Gambia, West Africa: a genomic analysis of vertical transmission

Clin Microbiol Infect. 2023 Mar;29(3):386.e1-386.e9. doi: 10.1016/j.cmi.2022.10.012. Epub 2022 Oct 13.

Abstract

Objectives: To define bacterial aetiology of neonatal sepsis and estimate the prevalence of neonatal infection from maternal genital tract bacterial carriage among mother-newborn pairs.

Methods: We carried out a cross-sectional study of newborns with clinical sepsis admitted to three hospitals in the Gambia neonatal wards. Neonatal blood cultures and maternal genital swabs were obtained at recruitment. We used whole-genome sequencing to explore vertical transmission for neonates with microbiologically confirmed bloodstream infection by comparing phenotypically-matched paired neonatal blood cultures and maternal genital tract bacterial isolates.

Results: We enrolled 203 maternal-newborn pairs. Two-thirds (67%; 137/203) of neonates presented with early-onset sepsis (days 0-6 after birth) of which 26% (36/137) were because of a clinically-significant bacterial pathogen. Blood culture isolates from newborns with early-onset sepsis because of Staphylococcus aureus (n = 5), Klebsiella pneumonia (n = 2), and Enterococcus faecalis (n = 1), phenotypically matched their maternal genital tract isolates. Pairwise single-nucleotide variants comparisons showed differences of 12 to 52 single-nucleotide variants only between maternal and newborn S. aureus isolates, presumably representing vertical transmission with a transmission rate of 14% (5/36).

Conclusions: We found a low prevalence of vertical transmission of maternal genital tract colonization in maternal-newborn pairs for early-onset neonatal sepsis in the West African context. Identifying infection acquisition pathways among newborns is essential to prioritize preventive interventions, which could be targeted at the mother or infection control in the hospital environment, depending on the major pathways of transmission.

Keywords: Early-onset; Maternal colonization; Neonatal sepsis; Vertical transmission; West Africa; Whole-genome sequencing.

MeSH terms

  • Africa, Western
  • Bacteria
  • Cross-Sectional Studies
  • Female
  • Gambia
  • Genomics
  • Humans
  • Infant, Newborn
  • Infant, Newborn, Diseases* / etiology
  • Infant, Newborn, Diseases* / microbiology
  • Infectious Disease Transmission, Vertical / prevention & control
  • Neonatal Sepsis*
  • Nucleotides
  • Sepsis* / epidemiology
  • Staphylococcus aureus

Substances

  • Nucleotides