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首页> 外文期刊>Journal of Clinical Microbiology >Detection of Chlamydia trachomatis infection in urine samples from men and women by ligase chain reaction.
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Detection of Chlamydia trachomatis infection in urine samples from men and women by ligase chain reaction.

机译:通过连接酶链反应检测男女尿样中的沙眼衣原体感染。

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摘要

The suitability of urine specimens from women and men for the detection of Chlamydia trachomatis infection by a ligase chain reaction (LCR)-based assay with plasmid primers was examined with a group of patients attending a sexually transmitted disease clinic in Amsterdam, The Netherlands. Cervical specimens from 15 of 237 (6.3%) women tested positive for C. trachomatis by cell culture. Of the 25 (10.5%) female urine samples that tested positive by the plasmid-LCR assay, 13 were obtained from cervical culture-positive women. Nine of the 12 plasmid-LCR-positive urine samples from cervical culture-negative women were confirmed to be positive by a second LCR assay with primers based on chromosomal DNA. Urethral specimens from 24 of 258 (9.3%) men were positive for C. trachomatis infection by cell culture. Of the 25 (9.7%) urine samples that tested positive by plasmid-LCR, 20 were from culture-positive men. All five of the LCR-positive urine samples from culture-negative men were confirmed to be positive by the LCR with chromosomal DNA primers. Relative to cell culture, testing by plasmid-LCR analysis of male urine samples had a sensitivity of 83.3% and a specificity of 97.9%; after resolution of discordant samples, these values were 86.2 and 100%, respectively. In the study with women, the sensitivities of plasmid-LCR analysis of cervical and urine specimens in comparison with cervical cell culture were 93.3 and 86.7%, respectively. After resolution of discrepant samples, the sensitivities of the plasmid-LCR test for cervical swabs and female urine samples were 96.3 and 92.6%, respectively. These results indicate that the plasmid-LCR-based assay is a very reliable, sensitive, convenient test for the detection of C. trachomatis infection in female and male urine specimens.
机译:在荷兰阿姆斯特丹的一家性病门诊就诊的一组患者中,检查了男女尿样通过质粒引物通过基于连接酶链反应(LCR)的检测方法检测沙眼衣原体感染的适用性。 237位女性中有15位(6.3%)的宫颈标本通过细胞培养检测为沙眼衣原体阳性。在通过质粒LCR检测呈阳性的25个(10.5%)女性尿液样本中,有13个从宫颈培养阳性妇女中获得。通过基于染色体DNA的引物进行的第二次LCR检测,来自宫颈培养阴性妇女的12个质粒-LCR阳性尿液样本中有9个证实为阳性。 258位男性中有24位(9.3%)的尿道标本通过细胞培养对沙眼衣原体感染呈阳性。在通过质粒LCR检测呈阳性的25个(9.7%)尿液样本中,有20个来自培养阳性的男性。来自培养阴性男性的所有五个LCR阳性尿液样本均通过染色体DNA引物的LCR证实为阳性。相对于细胞培养,通过质粒-LCR分析检测男性尿液样本的灵敏度为83.3%,特异性为97.9%;分离出不一致的样品后,这些值分别为86.2和100%。在女性研究中,与宫颈细胞培养相比,宫颈和尿液样本的质粒-LCR分析灵敏度分别为93.3和86.7%。分离出差异样本后,质粒-LCR检测对宫颈拭子和女性尿液样本的敏感性分别为96.3和92.6%。这些结果表明,基于质粒-LCR的测定是一种非常可靠,灵敏,方便的检测方法,用于检测雌性和雄性尿样中的沙眼衣原体感染。

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