Cytomegalovirus (CMV)-encoded UL144 (truncated tumor necrosis factor receptor) and outcome of congenital CMV infection

Ravit Arav-Boger, Catherine A. Battaglia, Tiziana Lazzarotto, Liliana Gabrielli, Jian C. Zong, Gary S. Hayward, Marie Diener-West, Maria P. Landini

Research output: Contribution to journalArticle

Abstract

Background. Cytomegalovirus (CMV) is the most common congenital infection in humans. The effect of viral strains on the outcome of congenital CMV is debated. We evaluated whether UL144 polymorphisms in amniotic fluid from CMV-infected Italian women were associated with terminations of pregnancy, subsequent disease in their offspring, or viral load. Methods. The study was nested within a prenatal CMV program. We sequenced the UL144 gene from 66 amniotic-fluid samples, without knowledge of pregnancy outcome. We performed data analyses on 56 samples for which all information was available. Results. Genotype C was associated with termination of pregnancy (P = .03). Genotype B was associated with fewer terminations of pregnancy (P = .003). A possible association was found between genotype C and symptomatic disease in newborns (odds ratio, 8.81 [95% confidence interval, 0.48-164.02]; P = .05). There was no association between specific genotype and the viral load in amniotic fluid. Symptomatic newborns who had the most common UL144 genotype (B) were more likely to have higher viral loads than were asymptomatic infants (P = .003). Conclusions. UL144 polymorphisms may be associated with the outcome of congenital CMV infection. Larger studies should be conducted to confirm this association, before genotype analysis can be used, along with other factors, in considering terminations of pregnancy.

Original languageEnglish (US)
Pages (from-to)464-473
Number of pages10
JournalJournal of Infectious Diseases
Volume194
Issue number4
DOIs
StatePublished - Aug 15 2006

ASJC Scopus subject areas

  • Immunology and Allergy
  • Infectious Diseases

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