Division of Global Epidemiology, Hokkaido University Research Center for Zoonosis Control, Sapporo, Hokkaido, Japan.
J Clin Microbiol. 2013 Jul;51(7):2025-32. doi: 10.1128/JCM.03404-12. Epub 2013 Apr 17.
The Beijing genotype of Mycobacterium tuberculosis is known to be a worldwide epidemic clade. It is suggested to be a possibly resistant clone against BCG vaccination and is also suggested to be highly pathogenic and prone to becoming drug resistant. Thus, monitoring the prevalence of this lineage seems to be important for the proper control of tuberculosis. The Rv0679c protein of M. tuberculosis has been predicted to be one of the outer membrane proteins and is suggested to contribute to host cell invasion. Here, we conducted a sequence analysis of the Rv0679c gene using clinical isolates and found that a single nucleotide polymorphism, C to G at position 426, can be observed only in the isolates that are identified as members of the Beijing genotype family. Here, we developed a simple multiplex PCR assay to detect this point mutation and applied it to 619 clinical isolates. The method successfully distinguished Beijing lineage clones from non-Beijing strains with 100% accuracy. This simple, quick, and cost-effective multiplex PCR assay can be used for a survey or for monitoring the prevalence of Beijing genotype M. tuberculosis strains.
结核分枝杆菌北京基因型已知是一种全球性流行的分支。它被认为是对卡介苗接种具有潜在耐药性的克隆,也被认为具有高致病性且易于产生耐药性。因此,监测该谱系的流行情况似乎对于结核病的适当控制非常重要。结核分枝杆菌的 Rv0679c 蛋白被预测为一种外膜蛋白,被认为有助于宿主细胞入侵。在这里,我们使用临床分离株对 Rv0679c 基因进行了序列分析,发现只有在被鉴定为北京基因型家族成员的分离株中才能观察到第 426 位的单核苷酸多态性,即 C 到 G。在这里,我们开发了一种简单的多重 PCR 检测方法来检测该点突变,并将其应用于 619 例临床分离株。该方法能够以 100%的准确率将北京谱系克隆与非北京菌株区分开来。这种简单、快速且具有成本效益的多重 PCR 检测方法可用于调查或监测北京基因型结核分枝杆菌菌株的流行情况。