Spurgiesz R Scott, Quitugua Teresa N, Smith Kimothy L, Schupp James, Palmer Eldon G, Cox Rebecca A, Keim Paul
Department of Biological Sciences, Northern Arizona University, Flagstaff, Arizona 86011-5640, USA.
J Clin Microbiol. 2003 Sep;41(9):4224-30. doi: 10.1128/JCM.41.9.4224-4230.2003.
Molecular epidemiological tools for genotyping clinical isolates of Mycobacterium tuberculosis have been developed and used to help track and contain transmission of tuberculosis. We identified 87 short sequence repeat loci within the genome of the M. tuberculosis H37Rv strain. Nine tandem repeats were found to be variable (variable-number tandem repeats [VNTRs]) in a set of 91 isolates. Fifty-seven of the isolates had only four IS6110 bands. The other 34 isolates were members of the Beijing strain family. The number of alleles of each these nine VNTRs was determined by examining each isolate. Six of the loci (Mtb-v1, -v4, -v10, -v15, -v18, and -v20) were able to differentiate the Beijing spoligotype identical isolates into seven distinct genotypes. Five of the loci (Mtb-v3, -v5, -v6, -v10, and -v15) were informative in discriminating the four-band IS6110 restriction fragment length polymorphism isolates from each other. The Nei's diversity values of each marker ranged from 0.02 to 0.59, with the number of alleles ranging from two to eight across the entire strain set. These nine loci provide a useful, discriminatory extension of VNTR typing methods for application to molecular epidemiologic studies of M. tuberculosis.
用于结核分枝杆菌临床分离株基因分型的分子流行病学工具已经得到开发,并用于帮助追踪和控制结核病的传播。我们在结核分枝杆菌H37Rv菌株的基因组中鉴定出87个短序列重复位点。在一组91株分离株中发现9个串联重复序列是可变的(可变数目串联重复序列[VNTR])。其中57株分离株只有4条IS6110条带。另外34株分离株属于北京菌株家族。通过检查每株分离株确定这9个VNTR中每个的等位基因数量。其中6个位点(Mtb-v1、-v4、-v10、-v15、-v18和-v20)能够将北京型寡核苷酸分型相同的分离株区分为7种不同的基因型。5个位点(Mtb-v3、-v5、-v6、-v10和-v15)在区分具有4条条带的IS6110限制性片段长度多态性分离株方面具有信息价值。每个标记的Nei多样性值范围为0.02至0.59,在整个菌株组中等位基因数量范围为2至8个。这9个位点为VNTR分型方法提供了一种有用的、具有鉴别力的扩展,可应用于结核分枝杆菌的分子流行病学研究。