Sahadevan R, Narayanan S, Paramasivan C N, Prabhakar R, Narayanan P R
Department of Immunology, Tuberculosis Research Centre, Chetput, Madras, India.
J Clin Microbiol. 1995 Nov;33(11):3037-9. doi: 10.1128/jcm.33.11.3037-3039.1995.
Large numbers of Mycobacterium tuberculosis isolates that were obtained from patients' sputa on diagnosis and during follow-up after short-course chemotherapy in Madras, India, have either no copy or only a single copy of IS6110. This poses a limitation for DNA fingerprinting with an IS6110-based probe to determine the frequency of exogenous reinfection versus that of endogenous reactivation. In the present study, we overcame this limitation by using an alternate probe, the direct-repeat element. Comparison of pre- and posttreatment isolates by direct-repeat restriction fragment length polymorphism analysis indicated a high degree of endogenous reactivation among patients who have relapses after the successful completion of chemotherapy.
从印度马德拉斯的患者痰液中分离出的大量结核分枝杆菌菌株,在诊断时以及短程化疗后的随访期间,要么没有IS6110拷贝,要么只有一个IS6110拷贝。这给使用基于IS6110的探针进行DNA指纹识别以确定外源性再感染与内源性再激活的频率带来了限制。在本研究中,我们通过使用另一种探针——直接重复元件克服了这一限制。通过直接重复限制性片段长度多态性分析对治疗前和治疗后的分离株进行比较,结果表明,在化疗成功完成后复发的患者中,内源性再激活程度很高。