EA4438 Physiopathologie et Médecine Translationnelle, Université de Strasbourg, Institut de Médecine Légale, 11 rue Humann, Strasbourg 67 085, France.
J Clin Microbiol. 2010 May;48(5):1758-66. doi: 10.1128/JCM.02255-09. Epub 2010 Mar 10.
The aim of the present study was to investigate the use of the SNaPshot minisequencing method for the identification of Mycobacterium tuberculosis complex (MTBC) isolates to the species level and for further genotyping of M. tuberculosis isolates. We developed an innovative strategy based on two multiplex allele-specific minisequencing assays that allowed detection of eight species-specific and eight lineage-specific single nucleotide polymorphisms (SNPs). Each assay consisted of an eightplex PCR amplification, followed by an eightplex minisequencing reaction with the SNaPshot multiplex kit (Applied Biosystems) and, finally, analysis of the extension products by capillary electrophoresis. The whole strategy was developed with a panel of 56 MTBC strains and 15 negative controls. All MTBC strains tested except one M. africanum clinical isolate were accurately identified to the species level, and all M. tuberculosis isolates were successfully further genotyped. This two-step strategy based on SNaPshot minisequencing allows the simultaneous differentiation of closely related members of the MTBC, the distinction between principal genetic groups, and the characterization of M. tuberculosis isolates into one of the seven prominent SNP cluster groups (SCGs) and could be a useful tool for diagnostic and epidemiological purposes.
本研究旨在探讨 SNaPshot 微测序方法在结核分枝杆菌复合群(MTBC)种水平鉴定和结核分枝杆菌分离株进一步基因分型中的应用。我们开发了一种基于两个多重等位基因特异性微测序检测的创新策略,可检测 8 个种特异性和 8 个谱系特异性单核苷酸多态性(SNPs)。每个检测由 8 重 PCR 扩增组成,随后进行 8 重 SNaPshot 多重试剂盒(Applied Biosystems)微测序反应,最后通过毛细管电泳分析延伸产物。整个策略是用一组 56 株 MTBC 菌株和 15 个阴性对照开发的。除了一株非洲分枝杆菌临床分离株外,所有测试的 MTBC 菌株均准确鉴定到种水平,所有结核分枝杆菌分离株均成功进行了进一步基因分型。这种基于 SNaPshot 微测序的两步策略可同时区分 MTBC 的密切相关成员,区分主要遗传群,并将结核分枝杆菌分离株分为 7 个主要 SNP 聚类群(SCG)之一,可作为诊断和流行病学目的的有用工具。