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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†

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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)的基因分型目前是用于研究结核分枝杆菌的分子流行病学和系统发育的非常有前途的工具。在这里,我们调查了先前由我们小组确定的结核分枝杆菌中48个直接或串联重复序列基因座的多态性。 39个基因座,包括9个新的基因座,是多态的。十个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VNTR分型集,用于与基于IS6110的限制性片段长度多态性(RFLP)分型进行比较。 10个位点的VNTR集(可能提供> 2×109个等位基因组合)明显表现出比IS6110 RFLP方法更高的分辨能力,可分离出少于6个IS6110杂交带的结核分枝杆菌,而与IS6110 RFLP相比分辨率更高这些分离物具有五个以上的IS6110杂交带。在每种IS6110 RFLP类型中,许多VNTR基因座的等位基因多样性都不同。从10-VNTR集合推断出的遗传关系支持以下观点:结核分枝杆菌可能已从两个不同谱系(高和低IS6110拷贝数)演变而来。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分型实际上可用于结核分枝杆菌的分子流行病学和系统发育研究。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。

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