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用于麻风分枝杆菌菌株分子分型的多个多态性位点。

Multiple polymorphic loci for molecular typing of strains of Mycobacterium leprae.

作者信息

Groathouse Nathan A, Rivoire Becky, Kim Hansuk, Lee Hyeyoung, Cho Sang-Nae, Brennan Patrick J, Vissa Varalakshmi D

机构信息

Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado 80523-1682, USA.

出版信息

J Clin Microbiol. 2004 Apr;42(4):1666-72. doi: 10.1128/JCM.42.4.1666-1672.2004.

Abstract

The need for molecular tools for the differentiation of isolates of Mycobacterium leprae, the organism that causes leprosy, is urgent in view of the continuing high levels of new case detection, despite years of aggressive chemotherapy and the consequent reduction in the prevalence of leprosy. The slow onset of leprosy and the reliance on physical examination for detection of disease have restricted the epidemiological tracking necessary to understand and control transmission. Two genetic loci in several isolates of M. leprae have previously been demonstrated to contain variable-number tandem repeats (VNTRs). On the basis of these reports and the availability of the full genome sequence, multiple-locus VNTR analysis for strain typing has been undertaken. A panel of 11 short tandem repeat (STR) loci with repeat units of 1, 2, 3, 6, 12, 18, 21, and 27 bp from four clinical isolates of M. leprae propagated in armadillo hosts were screened by PCR. Fragment length polymorphisms were detected at 9 of the 11 loci by agarose gel electrophoresis. Sequencing of representative DNA products confirmed the presence of VNTRs between isolates. The application of nine new polymorphic STRs in conjunction with automated methods for electrophoresis and size determination allows greater discrimination between isolates of M. leprae and enhances the potential of this technique to track the transmission of leprosy.

摘要

尽管多年来进行了积极的化疗,麻风病的患病率也因此有所下降,但新病例的检出率仍然居高不下。鉴于此,对于用于区分麻风分枝杆菌(引起麻风病的病原体)分离株的分子工具的需求十分迫切。麻风病发病缓慢,且依赖体格检查来检测疾病,这限制了理解和控制传播所需的流行病学追踪。此前已证明,在几种麻风分枝杆菌分离株中的两个基因位点含有可变数目串联重复序列(VNTR)。基于这些报告以及全基因组序列的可得性,已开展多位点VNTR分析用于菌株分型。通过PCR筛选了一组来自在犰狳宿主中繁殖的4株麻风分枝杆菌临床分离株的11个短串联重复序列(STR)位点,其重复单元分别为1、2、3、6、12、18、21和27 bp。通过琼脂糖凝胶电泳在11个位点中的9个位点检测到片段长度多态性。代表性DNA产物的测序证实了分离株之间存在VNTR。将9个新的多态性STR与自动化电泳和大小测定方法结合应用,能够更好地区分麻风分枝杆菌分离株,并增强了该技术追踪麻风病传播的潜力。

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