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采用DNA探针快速检测儿科患者标本中的化脓性链球菌

Rapid detection of Streptococcus pyogenes in pediatric patient specimens by DNA probe.

作者信息

Steed L L, Korgenski E K, Daly J A

机构信息

Primary Children's Medical Center, University of Utah School of Medicine, Salt Lake City 84132.

出版信息

J Clin Microbiol. 1993 Nov;31(11):2996-3000. doi: 10.1128/jcm.31.11.2996-3000.1993.

Abstract

A chemiluminescent DNA probe test (Group A Streptococcus Direct Test; Gen-Probe, Inc., San Diego, Calif.) for rapid, direct detection of cRNA of Streptococcus pyogenes in throat swabs was compared with conventional culture and identification techniques. Throat swabs from 277 patients suspected of having streptococcal pharyngitis were examined. By DNA probe alone, 10 specimens were positive, 51 were positive by both assays, and 8 were positive by culture alone. Thus, DNA probe sensitivity, specificity, and positive and negative predictive values were 86, 95, 84, and 96%, respectively. Including an indeterminate category, sensitivity, specificity, and positive and negative predictive values were 89, 96, 86, and 97%, respectively. After discrepancy testing, these values for the raw data improved to 90, 98, 93, and 97%, respectively. None of the 24 specimens that grew non-S. pyogenes beta-hemolytic streptococci in culture were positive by the DNA probe. Because mucoid S. pyogenes strains are more virulent than nonmucoid strains, 24 isolates were retrospectively tested with the DNA probe to ensure that both types would be detected equally well. Isolates were examined in pure cultures as well as mixed with representative normal oral flora. There was no statistical difference in detection of any of the four groups. Group A Streptococcus Direct Test is a rapid, sensitive, and specific test for S. pyogenes.

摘要

一种用于快速直接检测咽拭子中化脓性链球菌cRNA的化学发光DNA探针检测法(A组链球菌直接检测法;Gen-Probe公司,加利福尼亚州圣地亚哥)与传统培养和鉴定技术进行了比较。对277例疑似患有链球菌性咽炎的患者的咽拭子进行了检查。仅通过DNA探针检测,10份标本呈阳性,两种检测方法均呈阳性的有51份,仅培养呈阳性的有8份。因此,DNA探针的敏感性、特异性、阳性预测值和阴性预测值分别为86%、95%、84%和96%。包括不确定类别在内,敏感性、特异性、阳性预测值和阴性预测值分别为89%、96%、86%和97%。经过差异检测后,原始数据的这些值分别提高到90%、98%、93%和97%。在培养中生长出非化脓性链球菌β溶血性链球菌的24份标本中,没有一份通过DNA探针检测呈阳性。由于黏液样化脓性链球菌菌株比非黏液样菌株更具毒性,对24株分离株进行了回顾性DNA探针检测,以确保能同等良好地检测到这两种类型。对分离株进行了纯培养检查,以及与代表性口腔正常菌群混合后的检查。四组中任何一组的检测均无统计学差异。A组链球菌直接检测法是一种针对化脓性链球菌的快速、灵敏且特异的检测方法。

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