A CLINICAL AND EPIDEMIOLOGIC-STUDY OF HUMAN PARVOVIRUS B19 INFECTION IN FETAL HYDROPS USING PCR SOUTHERN BLOT HYBRIDIZATION AND CHEMILUMINESCENCE DETECTION
P. Wattre et al., A CLINICAL AND EPIDEMIOLOGIC-STUDY OF HUMAN PARVOVIRUS B19 INFECTION IN FETAL HYDROPS USING PCR SOUTHERN BLOT HYBRIDIZATION AND CHEMILUMINESCENCE DETECTION, Journal of medical virology, 54(2), 1998, pp. 140-144
Ninety-eight samples from 80 cases of spontaneous abortions after feta
l death or hydrops fetalis from 12,000 pregnant women were examined us
ing PCR. DNA was extracted from amniotic fluid, fetal blood, ascitic f
luid and fetal biopsies or placenta specimens using QIA amp kits (QIAG
EN). A 270-bp length fragment located within the B19 gene NS1 was ampl
ified using PCR followed by electrophoresis and southern-blot hybridiz
ation assay using a horseradish peroxidase-labelled probe and chemilum
inescence detection. This assay was able to detect 1 to 10 DNA copies
in a 10 mu l sample. Parvovirus B19 was identified in 11 cases (14% of
fetal hydrops; 1 case for 1,100 pregnancies). Amniotic fluid was the
most common and reliable sample to assess the diagnosis. Gestational a
ge ranged from 17 to 28 weeks (mean 23 weeks). IgM antibodies were det
ected in 3 maternal sera, 2 patients of which reported an exposure to
B19 infection during pregnancy. In 2 cases, intrauterine blood transfu
sions led to the cessation of symptoms and to birth of normal babies.
(C) 1998 Wiley-Liss, Inc.