Kurabachew Mekonnen, Enger Øivind, Sandaa Ruth Anne, Lemma Eshetu, Bjorvatn Bjarne
Centre for International Health, University of Bergen, Armauer Hansen Building, N-5021, Bergen, Norway.
J Microbiol Methods. 2003 Oct;55(1):83-90. doi: 10.1016/s0167-7012(03)00119-2.
This study explores the potential of the amplified ribosomal DNA restriction analysis (ARDRA) for intra- and interspecies identification of the genus Mycobacteria. A set of primers was used to amplify part of the 16S and 23S rDNA as well as the 16S-23S rDNA spacer from 121 isolates belonging to 13 different mycobacterial species. Restriction analysis was carried out with five different restriction enzymes, namely CfoI, HaeIII, RsaI, MspI and TaqI. Restriction digestion of the PCR product using CfoI enabled differentiation between 9 of the 13 mycobacterial species, whereas the remaining four enzymes differentiated between 7 of these 13 species. None of the five enzymes distinguished between different isolates of Mycobacterium tuberculosis or between species within the M. tuberculosis complex i.e., M. tuberculosis, M. bovis, M. bovis BCG and M. africanum. Although ARDRA analysis of the 16S-23S rDNA does not seem to have a potential for intraspecies differentiation, it has proven to be a rapid and technically relatively simple method to recognise strains belonging to the M. tuberculosis complex as well as to identify mycobacterial species outside this complex.
本研究探讨了扩增核糖体DNA限制性分析(ARDRA)在分枝杆菌属种内和种间鉴定中的潜力。使用一组引物扩增了121株属于13种不同分枝杆菌的16S和23S rDNA以及16S - 23S rDNA间隔区的部分片段。使用五种不同的限制性内切酶进行限制性分析,即CfoI、HaeIII、RsaI、MspI和TaqI。使用CfoI对PCR产物进行限制性消化能够区分13种分枝杆菌中的9种,而其余四种酶能够区分这13种中的7种。这五种酶均无法区分结核分枝杆菌的不同分离株,也无法区分结核分枝杆菌复合群内的物种,即结核分枝杆菌、牛分枝杆菌、卡介苗和非洲分枝杆菌。尽管对16S - 23S rDNA进行ARDRA分析似乎没有种内区分的潜力,但它已被证明是一种快速且技术上相对简单的方法,可用于识别属于结核分枝杆菌复合群的菌株以及鉴定该复合群之外的分枝杆菌物种。