Bobo L, Coutlee F, Yolken R H, Quinn T, Viscidi R P
Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
J Clin Microbiol. 1990 Sep;28(9):1968-73. doi: 10.1128/jcm.28.9.1968-1973.1990.
A sensitive and specific system for detection of amplified Chlamydia trachomatis DNA from cervical specimens by fluorometric quantitation in an enzyme immunoassay (EIA) format (polymerase chain reaction [PCR]-EIA) is described. The primers selected for PCR-amplified DNA were from the 15 serovars of C. trachomatis and two strains of Chlamydia pneumoniae (TWAR). One strain of Chlamydia psittaci (Borg) was not amplified. One hundred four previously cultured cervical specimens were evaluated. Forty-six culture-positive specimens containing from 1+ to 4+ inclusion bodies were all positive by PCR-EIA. Of 58 culture-negative specimens, 2 were repeatedly positive and were nonreactive with control probes. This assay system represents a sensitive and specific combination of technologies for the quantitative detection of C. trachomatis DNA directly from a body fluid.
本文描述了一种灵敏且特异的系统,该系统采用酶免疫分析(EIA)形式(聚合酶链反应[PCR]-EIA)通过荧光定量检测宫颈标本中沙眼衣原体DNA的扩增情况。用于PCR扩增DNA的引物来自沙眼衣原体的15个血清型以及两株肺炎衣原体(TWAR)。一株鹦鹉热衣原体(博尔格)未被扩增。对104份先前培养的宫颈标本进行了评估。46份培养阳性标本,包含1+至4+个包涵体,经PCR-EIA检测均为阳性。在58份培养阴性标本中,有2份反复呈阳性且与对照探针无反应。该检测系统代表了一种灵敏且特异的技术组合,可直接从体液中定量检测沙眼衣原体DNA。