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前瞻性地普遍应用分枝杆菌插入重复单元可变数目串联重复序列基因分型来鉴定结核分枝杆菌分离株,以便快速识别聚集性病例和散发病例。

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.

作者信息

Alonso-Rodriguez Noelia, Martínez-Lirola Miguel, Sánchez M Luisa, Herranz Marta, Peñafiel Teresa, Bonillo Magdalena del Carmen, Gonzalez-Rivera Milagros, Martínez Juan, Cabezas Teresa, Diez-García Luis Felipe, Bouza Emilio, García de Viedma Darío

机构信息

Servicio de Microbiología, Hospital Gregorio Marañón, Madrid, Spain.

出版信息

J Clin Microbiol. 2009 Jul;47(7):2026-32. doi: 10.1128/JCM.02308-08. Epub 2009 May 20.

Abstract

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.

摘要

在流行病学调查中,为了识别聚集性菌株和孤儿菌株而使用分子工具对结核分枝杆菌分离株进行基因分型,需要比参考方法——IS6110限制片段长度多态性(RFLP)基因分型更快的响应时间。一种基于聚合酶链反应(PCR)的方法,即分枝杆菌散布重复单位可变数目串联重复序列(MIRU-VNTR)基因分型技术,是对结核分枝杆菌进行快速指纹识别的一种选择,不过在转换方法之前,需要在不同背景下基于人群的研究中对MIRU-VNTR与RFLP结果之间的相关性进行精确评估。在本研究中,我们在一项为期39个月、基于普遍人群的研究中,在一个移民比例很高的具有挑战性的环境中,将MIRU-VNTR基因分型(使用一组15个位点 [MIRU-15])与RFLP基因分型并行进行评估。对于81.9%(281/343)的结核分枝杆菌分离株,同时获得了RFLP和MIRU-VNTR分型结果。RFLP分析和MIRU-15分析中聚集性病例的百分比分别为39.9%(112/281)和43.1%(121/281),识别出的聚集簇数量分别为42个和45个。对于85.4%的病例,RFLP和MIRU-15结果一致,将相同的病例识别为聚集性和孤儿病例(kappa值为0.7)。然而,对于其余14.6%的病例,观察到了差异:RFLP分析聚类的16例病例被MIRU-15分析识别为孤儿病例,RFLP分析识别为孤儿病例的25例病例被MIRU-15分析聚类。当容忍显示细微基因型差异的不一致病例时,差异从14.6%降至8.6%。通过RFLP和MIRU-15分析聚类的病例中,83.8%发现了流行病学联系,而对于仅通过RFLP或MIRU-VNTR分析聚类的病例,分别仅在30.8%或38.9%的病例中发现了联系。后一组病例主要包括那些如果容忍细微基因型差异也可能被聚类的分离株。对于实时干预方案,MIRU-15基因分型似乎是RFLP基因分型的一个很好的替代方法。MIRU-15与IS6110 RFLP结果之间的相关性是合理的,尽管在通过MIRU-15分析进行聚类分配方面存在一些不确定性。

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