Aranaz A, Liébana E, Mateos A, Domínguez L, Cousins D
Dpto. Patología Animal I (Sanidad Animal), Facultad de Veterinaria UCM, Madrid, Spain.
Vet Microbiol. 1998 Apr 15;61(4):311-24. doi: 10.1016/s0378-1135(98)00192-8.
The combination of conventional investigation and DNA fingerprinting is yielding important insights into the epidemiology of Mycobacterium bovis infections. Various genetic markers used in restriction fragment length polymorphism (RFLP) have recently been exploited for fingerprinting of M. bovis isolates. The newly developed spacer oligonucleotide typing aimed to investigate the polymorphism of M. tuberculosis in the DR locus, has also been applied to the molecular typing of M. bovis isolates. This work compared the performance of the insertion sequence (IS) IS6110, IS1081 and the genetic elements polymorphic G + C-rich repeat (PGRS) and direct repeat (DR) used in RFLP analysis with spoligotyping using a group of 128 Spanish M. bovis isolates. In this study, the most sensitive technique for identifying polymorphism in M. bovis was PGRS-RFLP, closely followed by IS6110-RFLP. We propose several schemes for fingerprinting of these isolates, however, the clear geographical variations found by different authors makes the study of each local situation indispensable. An international consensus in the methods used would be desirable for efficient interlaboratory comparison of strains.
传统调查与DNA指纹图谱技术相结合,正在为牛分枝杆菌感染的流行病学研究提供重要见解。限制片段长度多态性(RFLP)中使用的各种遗传标记最近已被用于牛分枝杆菌分离株的指纹图谱分析。新开发的间隔寡核苷酸分型旨在研究结核分枝杆菌DR位点的多态性,也已应用于牛分枝杆菌分离株的分子分型。这项工作使用一组128株西班牙牛分枝杆菌分离株,比较了插入序列(IS)IS6110、IS1081以及RFLP分析中使用的遗传元件多态性富含G + C重复序列(PGRS)和直接重复序列(DR)与间隔寡核苷酸分型的性能。在本研究中,鉴定牛分枝杆菌多态性最敏感的技术是PGRS-RFLP,其次是IS6110-RFLP。我们提出了几种这些分离株的指纹图谱方案,然而,不同作者发现的明显地理差异使得对每个当地情况的研究不可或缺。为了实现菌株的高效实验室间比较,在使用的方法上达成国际共识将是可取的。