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首页> 外文期刊>Journal of Clinical Microbiology >Prospective Universal Application of Mycobacterial Interspersed Repetitive-Unit-Variable-Number Tandem-Repeat Genotyping To Characterize Mycobacterium tuberculosis Isolates for Fast Identification of Clustered and Orphan Cases
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Prospective Universal Application of Mycobacterial Interspersed Repetitive-Unit-Variable-Number Tandem-Repeat Genotyping To Characterize Mycobacterium tuberculosis Isolates for Fast Identification of Clustered and Orphan Cases

机译:分枝杆菌散布的重复单位可变数串联重复基因分型的前瞻性普遍应用,以表征结核分枝杆菌分离株,用于快速鉴定集群和孤儿病例

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The use of molecular tools for genotyping Mycobacterium tuberculosis isolates in epidemiological surveys in order to identify clustered and orphan strains requires faster response times than those offered by the reference method, IS6110 restriction fragment length polymorphism (RFLP) genotyping. A method based on PCR, the mycobacterial interspersed repetitive-unit-variable-number tandem-repeat (MIRU-VNTR) genotyping technique, is an option for fast fingerprinting of M. tuberculosis, although precise evaluations of correlation between MIRU-VNTR and RFLP findings in population-based studies in different contexts are required before the methods are switched. In this study, we evaluated MIRU-VNTR genotyping (with a set of 15 loci [MIRU-15]) in parallel to RFLP genotyping in a 39-month universal population-based study in a challenging setting with a high proportion of immigrants. For 81.9% (281/343) of the M. tuberculosis isolates, both RFLP and MIRU-VNTR types were obtained. The percentages of clustered cases were 39.9% (112/281) and 43.1% (121/281) for RFLP and MIRU-15 analyses, and the numbers of clusters identified were 42 and 45, respectively. For 85.4% of the cases, the RFLP and MIRU-15 results were concordant, identifying the same cases as clustered and orphan (kappa, 0.7). However, for the remaining 14.6% of the cases, discrepancies were observed: 16 of the cases clustered by RFLP analysis were identified as orphan by MIRU-15 analysis, and 25 cases identified as orphan by RFLP analysis were clustered by MIRU-15 analysis. When discrepant cases showing subtle genotypic differences were tolerated, the discrepancies fell from 14.6% to 8.6%. Epidemiological links were found for 83.8% of the cases clustered by both RFLP and MIRU-15 analyses, whereas for the cases clustered by RFLP or MIRU-VNTR analysis alone, links were identified for only 30.8% or 38.9% of the cases, respectively. The latter group of cases mainly comprised isolates that could also have been clustered, if subtle genotypic differences had been tolerated. MIRU-15 genotyping seems to be a good alternative to RFLP genotyping for real-time interventional schemes. The correlation between MIRU-15 and IS6110 RFLP findings was reasonable, although some uncertainties as to the assignation of clusters by MIRU-15 analysis were identified.
机译:在流行病学调查中使用分子工具对结核分枝杆菌菌株进行基因分型以鉴定聚集和孤儿菌株需要比参考方法IS 6110 限制方法更快的响应时间片段长度多态性(RFLP)基因分型。一种基于PCR的方法,即分枝杆菌散布的重复单位可变数目串联重复(MIRU-VNTR)基因分型技术,是对 M进行快速指纹识别的一种选择。结核病,但是在切换方法之前,需要在不同背景下基于人群的研究中准确评估MIRU-VNTR和RFLP结果之间的相关性。在这项研究中,我们在一项具有挑战性的,移民比例很高的环境下进行的为期39个月的以人群为基础的研究中,与RFLP基因分型同时评估了MIRU-VNTR基因分型(带有15个基因座[MIRU-15])。对于 M的81.9%(281/343)。获得了结核分枝杆菌,RFLP和MIRU-VNTR类型。对于RFLP和MIRU-15分析,聚类病例的百分比分别为39.9%(112/281)和43.1%(121/281),识别出的聚类数目分别为42和45。对于85.4%的病例,RFLP和MIRU-15的结果一致,确定为聚类和孤儿(kappa,0.7)。然而,在其余14.6%的病例中,观察到差异:通过MIRU-15分析将16个通过RFLP分析聚类的病例鉴定为孤儿,通过MIRU-15分析将25个通过RFLP分析鉴定为孤儿病例。当容忍表现出细微基因型差异的差异病例时,差异从14.6%降至8.6%。通过RFLP和MIRU-15分析发现,有83.8%的病例具有流行病学联系,而仅通过RFLP或MIRU-VNTR分析进行聚类的病例,仅发现了30.8%或38.9%的联系。后一组病例主要是分离株,如果可以容忍细微的基因型差异,它们也可以聚类。对于实时干预方案,MIRU-15基因分型似乎是RFLP基因分型的良好选择。 MIRU-15和 IS6110 RFLP结果之间的相关性是合理的,尽管通过MIRU-15分析确定了簇的分配存在一些不确定性。

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