Jalal Hamid, Stephen Hannah, Alexander Sarah, Carne Christopher, Sonnex Christopher
Clinical Microbiology & Public Health Laboratory, Box 236, Addenbrooke's Hospital, Hills Road, Cambridge CB2 2QW, United Kingdom.
J Clin Microbiol. 2007 Aug;45(8):2649-53. doi: 10.1128/JCM.00451-07. Epub 2007 Jun 13.
We have developed and validated a nested real-time PCR (NRT-PCR) for the genotyping of Chlamydia trachomatis and used it specifically for the typing of either eight genovars from D to K or three genovars of lymphogranuloma venereum (LGV). The 11 probes used in the NRT-PCR correctly identified the DNA from D to K and LGV reference strains and did not cross-react with the DNA from 26 strains representing the bacterial pathogens and commensals of the oropharynx, genital tract, and rectum. The NRT-PCR had a 95% probability of detection at four genome copies (confidence interval, three to six copies) of C. trachomatis per reaction. One hundred cervical and urethral swab specimens containing C. trachomatis DNA from 63 women and 37 men were used to validate the method. The results from the NRT-PCR and the DNA sequencing of amplicons generated from the omp1 gene showed 100% correlation for these samples. The assay also identified the LGV-II genotype in 24 of 48 rectal swab specimens containing C. trachomatis DNA that were obtained from men having sex with men. The Sexually Transmitted Bacteria Reference Laboratory, London, independently confirmed these results using group-specific LGV real-time PCR and restriction fragment length polymorphism analysis. Compared with the NRT-PCR, non-NRT-PCR was found to be less sensitive: it typed C. trachomatis DNA in only 80% of the genital samples and 90% of the rectal swab samples. This is the first successful demonstration of the use of real-time PCR for the genotype-specific typing of C. trachomatis strains that cause sexually transmitted diseases.
我们已研发并验证了一种用于沙眼衣原体基因分型的巢式实时聚合酶链反应(NRT-PCR),并将其专门用于对D至K的8个基因变种或性病性淋巴肉芽肿(LGV)的3个基因变种进行分型。NRT-PCR中使用的11种探针能够正确识别来自D至K以及LGV参考菌株的DNA,并且不会与代表口咽、生殖道和直肠的细菌病原体及共生菌的26种菌株的DNA发生交叉反应。NRT-PCR在每个反应中对四个沙眼衣原体基因组拷贝数(置信区间为三至六个拷贝)的检测概率为95%。使用来自63名女性和37名男性的100份含有沙眼衣原体DNA的宫颈和尿道拭子标本对该方法进行验证。NRT-PCR的结果与从omp1基因生成的扩增子的DNA测序结果在这些样本中显示出100%的相关性。该检测方法还在从男男性行为者中获得的48份含有沙眼衣原体DNA的直肠拭子标本中的24份中鉴定出了LGV-II基因型。伦敦性传播细菌参考实验室使用组特异性LGV实时聚合酶链反应和限制性片段长度多态性分析独立证实了这些结果。与NRT-PCR相比,发现非NRT-PCR的敏感性较低:它仅能对80%的生殖器样本和90%的直肠拭子样本中的沙眼衣原体DNA进行分型。这是首次成功证明使用实时聚合酶链反应对导致性传播疾病的沙眼衣原体菌株进行基因型特异性分型。