Pasternack R, Vuorinen P, Miettinen A
Department of Clinical Microbiology, Tampere University Hospital, Finland.
J Clin Microbiol. 1997 Mar;35(3):676-8. doi: 10.1128/jcm.35.3.676-678.1997.
We evaluated the Gen-Probe Chlamydia trachomatis transcription-mediated amplification (TMA) assay with urine specimens for the detection of C. trachomatis infections in women. The novel test, based on the isothermal amplification of chlamydial RNA, was compared with the Roche Amplicor PCR with urine and cell culture with endocervical specimens. First-catch urine and endocervical swab specimens were collected from a total of 561 patients, of whom 70 (12.3%) were confirmed to have chlamydial infection. The diagnostic sensitivity and specificity of TMA with urine were 91.4 and 99.6%, respectively, and those of Amplicor PCR were 97.1 and 99.8%, respectively. By repeated analysis of the specimens with discrepant results, the sensitivity of TMA could be increased to 99%, indicating that some methodological improvements in the assay are still to be expected. The sensitivity of PCR could be increased to 100% by the elimination of DNA polymerase inhibitors in a repeated analysis. The sensitivity and specificity of cell culture with cervical specimens were 85.7 and 100%, respectively. The results indicate that TMA with urine specimens from women is a sensitive and specific assay for the detection of C. trachomatis, providing a new noninvasive technique for the screening of chlamydial infections in women.
我们评估了Gen-Probe沙眼衣原体转录介导扩增(TMA)检测法在检测女性沙眼衣原体感染时对尿液标本的应用。这项基于衣原体RNA等温扩增的新检测法,与罗氏Amplicor PCR法检测尿液以及用宫颈标本进行细胞培养的方法进行了比较。从总共561名患者中收集了首次晨尿和宫颈拭子标本,其中70名(12.3%)被确诊为衣原体感染。尿液TMA检测法的诊断敏感性和特异性分别为91.4%和99.6%,Amplicor PCR法的诊断敏感性和特异性分别为97.1%和99.8%。通过对结果不一致的标本进行重复分析,TMA的敏感性可提高到99%,这表明该检测法在方法上仍有待进一步改进。通过在重复分析中消除DNA聚合酶抑制剂,PCR的敏感性可提高到100%。宫颈标本细胞培养的敏感性和特异性分别为85.7%和100%。结果表明,女性尿液标本的TMA检测法是一种检测沙眼衣原体的敏感且特异的检测方法,为女性沙眼衣原体感染筛查提供了一种新的非侵入性技术。