首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Direct detection of Chlamydia trachomatis in urine specimens from symptomatic and asymptomatic men by using a rapid polymerase chain reaction assay.
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Direct detection of Chlamydia trachomatis in urine specimens from symptomatic and asymptomatic men by using a rapid polymerase chain reaction assay.

机译:使用快速聚合酶链反应测定法直接检测有症状和无症状男性尿液样本中的沙眼衣原体。

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摘要

Screening for Chlamydia trachomatis infection in men has traditionally been limited to men who present with urethral symptoms, thereby limiting the detection of asymptomatic chlamydia infection in men. In order to effectively screen both symptomatic and asymptomatic men, we evaluated a newly developed polymerase chain reaction (PCR) assay, Amplicor C. trachomatis, from Roche Molecular Systems for the detection of C. trachomatis in urine specimens in comparison with urethral culture. A total of 530 male urine specimens were collected from 322 symptomatic and 208 asymptomatic men attending two sexually transmitted disease clinics in Baltimore, Md. The prevalence of C. trachomatis by culture was 9.8% (10.6% in symptomatic men and 8.2% in asymptomatic men). Compared with culture, the sensitivity of the PCR was 92.8%, the specificity was 94.7%, the positive predictive value was 68.4%, and the negative predictive value was 99.1%. Discrepant results between culture and PCR were further analyzed by direct fluorescent-antibody staining of elementary bodies in urine sediment and in culture transport vials and by major outer membrane protein PCR of transport media for specimens with negative culture. The revised sensitivity and specificity of PCR for urine were 95.0 and 99.8%, respectively, and the positive and negative predictive values were 98.7 and 99.1%, respectively. The sensitivity of culture compared with PCR and/or direct fluorescent-antibody staining was 68.4%. These results indicate that the PCR assay is a highly sensitive and specific assay for the detection of C. trachomatis in male urine specimens and provides a noninvasive technique for routine screening of chlamydia infection in both symptomatic and asymptomatic men.
机译:传统上,男性沙眼衣原体感染的筛查仅限于出现尿道症状的男性,从而限制了男性无症状衣原体感染的检测。为了有效筛查有症状和无症状的男性,我们评估了罗氏分子系统公司最新开发的聚合酶链反应(PCR)分析法Amplicor沙眼衣原体,用于检测尿液样本中的沙眼衣原体与尿道培养相比。从马里兰州巴尔的摩市两家性病门诊的322名有症状和208名有症状的男性中收集了530个男性尿液标本。通过培养,沙眼衣原体的患病率为9.8%(有症状的男性为10.6%,无症状的男性为8.2%。 )。与培养相比,PCR的敏感性为92.8%,特异性为94.7%,阳性预测值为68.4%,阴性预测值为99.1%。通过直接荧光抗体染色尿沉渣中和培养物运输小瓶中的基本体以及通过运输培养基的主要外膜蛋白PCR对带有阴性培养物的标本进一步分析了培养物与PCR之间的差异结果。经修订的尿液PCR灵敏度和特异性分别为95.0和99.8%,阳性和阴性预测值分别为98.7和99.1%。与PCR和/或直接荧光抗体染色相比,培养物的敏感性为68.4%。这些结果表明,PCR检测是检测男性尿液标本中沙眼衣原体的高度灵敏和特异的检测方法,为有症状和无症状男性的衣原体感染的常规筛查提供了一种非侵入性技术。

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