Dynamics of pregnancy-associated polyomavirus urinary excretion: A prospective longitudinal study

Asymptomatic polyomaviruria of pregnancy has been documented in point prevalence studies, but little attention has been given to the dynamics of polyomavirus excretion during pregnancy because of its benign course. We tested the hypothesis that the frequency and/or magnitude of polyomavirus excretio...

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Published inJournal of medical virology Vol. 84; no. 8; pp. 1312 - 1322
Main Authors McClure, Gloria B., Gardner, J. Suzette, Williams, Jason T., Copeland, Christina M., Sylvester, Sarah K., Garcea, Robert L., Meinerz, Natalie M., Groome, Lynn J., Vanchiere, John A.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.08.2012
Wiley
Wiley Subscription Services, Inc
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Summary:Asymptomatic polyomaviruria of pregnancy has been documented in point prevalence studies, but little attention has been given to the dynamics of polyomavirus excretion during pregnancy because of its benign course. We tested the hypothesis that the frequency and/or magnitude of polyomavirus excretion would increase as pregnancy progresses. Urine specimens were obtained prospectively from 179 healthy women during uncomplicated pregnancies and 37 healthy non‐pregnant women. Real‐time polymerase chain reaction was used to determine BK virus (BKV) and JC virus (JCV) viral loads in urine, blood, and rectal and vaginal swabs collected during routine obstetric and gynecologic clinic visits. Asymptomatic urinary shedding of BKV and/or JCV was observed in 384 (48.0%) of 800 specimens from 100 (55.8%) pregnant women. BKV excretion was more common in pregnant than non‐pregnant women (41.3% vs. 13.5%, P = 0.0026). The frequency of JCV excretion was no different in pregnant compared to non‐pregnant women. The frequency and magnitude of polyomavirus shedding did not vary with gestational age. Post‐partum shedding of BKV, but not JCV, rapidly decreased to undetectable levels. Pregnancy‐associated BKV excretion begins early in pregnancy and terminates rapidly post‐partum. Neither the frequency nor magnitude of BKV or JCV shedding increased with pregnancy progression. Further study into the host factors that regulate pregnancy‐associated BKV excretion may allow identification of the host factors that predict susceptibility to BKV‐associated diseases in immune compromised patients. J. Med. Virol. 84: 1312–1322, 2012. © 2012 Wiley Periodicals, Inc.
Bibliography:The authors have no conflicts of interest to disclose.
Department of Pediatrics at LSUHSC-S
ArticleID:JMV23320
istex:0B3D7234B63D004B828B62F44D0B68AC676789E4
ark:/67375/WNG-XZRLQWPM-0
National Center for Research Resources - No. 5P20RR018724-10
National Institute of General Medical Sciences (National Institutes of Health to the Center for Molecular and Tumor Virology at LSUHSC-S) - No. 8 P20 GM103433-10
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ObjectType-Article-2
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ISSN:0146-6615
1096-9071
DOI:10.1002/jmv.23320