首页> 外文期刊>Journal of Clinical Microbiology >Polymorphism of Variable-Number Tandem Repeats at Multiple Loci in Mycobacterium tuberculosis
【24h】

Polymorphism of Variable-Number Tandem Repeats at Multiple Loci in Mycobacterium tuberculosis

机译:结核分枝杆菌中多个位点的可变数目串联重复序列的多态性

获取原文
           

摘要

Genotyping based on variable-number tandem repeats (VNTR) is currently a very promising tool for studying the molecular epidemiology and phylogeny of Mycobacterium tuberculosis. Here we investigate the polymorphisms of 48 loci of direct or tandem repeats in M. tuberculosis previously identified by our group. Thirty-nine loci, including nine novel ones, were polymorphic. Ten VNTR loci had high allelic diversity (Nei's diversity indices ≥ 0.6) and subsequently were used as the representative VNTR typing set for comparison to IS6110-based restriction fragment length polymorphism (RFLP) typing. The 10-locus VNTR set, potentially providing >2 × 109 allele combinations, obviously showed discriminating capacity over the IS6110 RFLP method for M. tuberculosis isolates with fewer than six IS6110-hybridized bands, whereas it had a slightly better resolution than IS6110 RFLP for the isolates having more than five IS6110-hybridized bands. Allelic diversity of many VNTR loci varied in each IS6110 RFLP type. Genetic relationships inferred from the 10-VNTR set supported the notion that M. tuberculosis may have evolved from two different lineages (high and low IS6110 copy number). In addition, we found that the lengths of many VNTR loci had statistically significant relationships to each other. These relationships could cause a restriction of the VNTR typing discriminating capability to some extent. Our results suggest that VNTR-PCR typing is practically useful for application to molecular epidemiological and phylogenetic studies of M. tuberculosis. The discriminating power of the VNTR typing system can still be enhanced by the supplementation of more VNTR loci.
机译:基于可变数目串联重复序列(VNTR)的基因分型是目前研究结核分枝杆菌的分子流行病学和系统发生学的非常有前途的工具。在这里,我们研究了 M中48个直接或串联重复基因座的多态性。我们小组先前确定的结核病。 39个基因座,包括9个新的基因座,是多态的。 10个VNTR基因座具有较高的等位基因多样性(Nei多样性指数≥0.6),随后被用作代表性的VNTR分型集,与基于IS 6110 的限制性片段长度多态性(RFLP)分型进行比较。可能提供> 2×10 9 等位基因组合的10位VNTR集明显显示出对 M的IS 6110 RFLP方法的区分能力。 IS 6110 杂交带少于6条的结核病分离株,而IS 6110 RFLP超过5条的分离株的分离度稍好于IS 6110 RFLP。 em> 6110 杂交带。每个IS 6110 RFLP类型的许多VNTR基因座的等位基因多样性都不同。从10-VNTR集推断出的遗传关系支持 M的概念。结核病可能是由两个不同的系(IS 6110 拷贝数高和低)演变而来的。此外,我们发现许多VNTR基因座的长度在统计学上具有显着的相互关系。这些关系可能会在某种程度上导致VNTR类型识别能力受到限制。我们的结果表明,VNTR-PCR分型实际上可用于 M的分子流行病学和系统发育研究。结核病。通过补充更多的VNTR基因座,仍可以增强VNTR分型系统的辨别能力。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号