International Journal of Infectious Diseases (May 2022)

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

Journal volume & issue
Vol. 118
pp. 24 – 33

Abstract

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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 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 cerebrospinal fluid (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.

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