Takahashi S, Hagiwara T, Shiga S, Hirose T, Tsukamoto T
Department of Urology, Sapporo Medical University School of Medicine, South 1 West 16, Chuo-ku, Sapporo 060-8543, Japan.
J Infect Chemother. 2000 Dec;6(4):211-5. doi: 10.1007/s101560070005.
A polymerase chain reaction (PCR) method for the detection of Chlamydia trachomatis has been developed and is now available in the clinical setting. However, one of the major problems with this method is possible false-positive detection posttreatment. Nonviable C. trachomatis was established by in-vitro exposure to an antimicrobial agent, and we tried to detect the nonviable cells (NVCs) of C. trachomatis by PCR with variant primer sets. C. trachomatis strains (D/UW-3/Cx) were cultured in a medium containing the antimicrobial agent, at 8 x MIC (minimal inhibitory concentration) 15 to 20 h postinfection. Amplicor and two sets of PCR primers were used to detect the DNA of NVCs. Serial passages of NVCs were done five times. All samples were positive on Amplicor, and all except the fourth passage were positive for the two sets of primers. Although the PCR test appears to be valuable, NVCs may possibly be detected by this method, and this may be clinically responsible for the false detection of C. trachomatis after appropriate antimicrobial chemotherapy.
一种用于检测沙眼衣原体的聚合酶链反应(PCR)方法已被开发出来,目前可用于临床。然而,该方法的一个主要问题是治疗后可能出现假阳性检测结果。通过体外暴露于抗菌剂建立了无活力的沙眼衣原体,我们尝试用不同的引物组通过PCR检测沙眼衣原体的无活力细胞(NVCs)。沙眼衣原体菌株(D/UW-3/Cx)在含有抗菌剂的培养基中培养,感染后15至20小时达到8倍最小抑菌浓度(MIC)。使用Amplicor和两组PCR引物检测NVCs的DNA。NVCs连续传代五次。所有样本在Amplicor上均为阳性,除第四代外,两组引物检测均为阳性。尽管PCR检测似乎很有价值,但该方法可能会检测到NVCs,这在临床上可能导致在适当的抗菌化疗后沙眼衣原体的假阳性检测。