Cytomegalovirus infections in infants in Uganda: Newborn-mother pairs, neonates with sepsis, and infants with hydrocephalus

  • Christine Hehnly
  • , Paddy Ssentongo
  • , Lisa M. Bebell
  • , Kathy Burgoine
  • , Joel Bazira
  • , Claudio Fronterre
  • , Elias Kumbakumba
  • , Ronald Mulondo
  • , Edith Mbabazi-Kabachelor
  • , Sarah U. Morton
  • , Joseph Ngonzi
  • , Moses Ochora
  • , Peter Olupot-Olupot
  • , John Mugamba
  • , Justin Onen
  • , Drucilla J. Roberts
  • , Kathryn Sheldon
  • , Shamim A. Sinnar
  • , Jasmine Smith
  • , Peter Ssenyonga
  • Julius Kiwanuka, Joseph N. Paulson, Frederick A. Meier, Jessica E. Ericson, James R. Broach, Steven J. Schiff

Research output: Contribution to journalArticlepeer-review

Abstract

Objectives: To estimate the prevalence of cytomegalovirus (CMV) infections among newborn-mother pairs, neonates with sepsis, and infants with hydrocephalus in Uganda. Design and Methods: Three populations—newborn-mother pairs, neonates with sepsis, and infants (≤3 months) with nonpostinfectious (NPIH) or postinfectious (PIH) hydrocephalus—were evaluated for CMV infection at 3 medical centers in Uganda. Quantitative PCR (qPCR) was used to characterize the prevalence of CMV. Results: The overall CMV prevalence in 2498 samples in duplicate across all groups was 9%. In newborn-mother pairs, there was a 3% prevalence of cord blood CMV positivity and 33% prevalence of maternal vaginal shedding. In neonates with clinical sepsis, there was a 2% CMV prevalence. Maternal HIV seropositivity (adjusted odds ratio [aOR] 25.20; 95% confidence interval [CI] 4.43–134.26; p = 0.0001), residence in Eastern Uganda (aOR 11.06; 95% CI 2.30–76.18; p = 0.003), maternal age <25 years (aOR 4.54; 95% CI 1.40–19.29; p = 0.02), and increasing neonatal age (aOR 1.08 for each day older; 95% CI 1.00–1.16; p = 0.05), were associated risk factors for CMV in neonates with clinical sepsis. We found a 2-fold higher maternal vaginal shedding in eastern (45%) vs western (22%) Uganda during parturition (n = 22/49 vs 11/50, the Fisher exact test; p = 0.02). In infants with PIH, the prevalence in blood was 24% and in infants with NPIH, it was 20%. CMV was present in the CSF of 13% of infants with PIH compared with 0.5% of infants with NPIH (n = 26/205 vs 1/194, p < 0.0001). Conclusions: Our findings highlight that congenital and postnatal CMV prevalence is substantial in this African setting, and the long-term consequences are uncharacterized.

Original languageEnglish (US)
Pages (from-to)24-33
Number of pages10
JournalInternational Journal of Infectious Diseases
Volume118
DOIs
StatePublished - May 2022

All Science Journal Classification (ASJC) codes

  • Microbiology (medical)
  • Infectious Diseases

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