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Comparison of culture and 2 real-time polymerase chain reaction assays to detect group B Streptococcus during antepartum screening
被引:32
|作者:
Goodrich, Jennifer S.
Miller, Melissa B.
机构:
[1] Univ N Carolina, Sch Med, Dept Pathol & Lab Med, Chapel Hill, NC 27599 USA
[2] Univ N Carolina Hosp, Dept Pathol & Lab Med, Chapel Hill, NC USA
关键词:
group B streptococcus;
streptococcus agalactiae;
antepartum screening;
real-time PCR;
D O I:
10.1016/j.diagmicrobio.2007.03.023
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
Group B Streptococcus (GBS) is the most common cause of life-threatening infection in neonates but is preventable if the mother is diagnosed before and treated at delivery. Using 200 vaginal-rectal swabs inoculated to enrichment (LIM) broths, we compared routine culture and 2 real-time polymerase chain reaction (PCR) assays for detection of GBS: the LightCycler (LC) Strep B analyte-specific reagents (ASRs) (Roche Diagnostics, Indianapolis, IN) and the BD GeneOhm StrepB (BD-StrepB) test (BD GeneOhm Sciences, San Diego, CA). Culture detected 26.5% GBS-positive specimens, whereas the LC Strep B ASR and BD-StrepB test identified 29.5% and 30.0% positive specimens, respectively. Because of the increased detection rate of 3.0% to 3.5% observed with PCR, a second GBS-specific amplicon was sequenced to confirm the presence of GBS that was not detected by culture. In our hands, the sensitivity/specificity of the LC Strep B ASR was 100%/95.9%, and the BD-StrepB test was 92.5%/92.5% using culture as the gold standard. (c) 2007 Elsevier Inc. All rights reserved.
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页码:17 / 22
页数:6
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