EA4438 Physiopathologie et Médecine Translationnelle, Faculté de Médecine, Université de Strasbourg, Strasbourg, France.
J Clin Microbiol. 2011 Sep;49(9):3292-9. doi: 10.1128/JCM.00744-11. Epub 2011 Jul 6.
The major goal of the present study was to investigate the potential use of a novel single nucleotide polymorphism (SNP) genotyping technology, called iPLEX Gold (Sequenom), for the simultaneous analysis of 16 SNPs that have been previously validated as useful for identification of Mycobacterium tuberculosis complex (MTBC) species and classification of MTBC isolates into distinct genetic lineages, known as principal genetic groups (PGGs) and SNP cluster groups (SCGs). In this context, we developed a 16-plex iPLEX assay based on an allele-specific-primer single-base-extension reaction using the iPLEX Gold kit (Sequenom), followed by matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) analysis on the commercially available Sequenom MassARRAY platform. This assay was tested on a panel of 55 well-characterized MTBC strains that were also genotyped for the same loci using the previously reported SNaPshot assay, as well as 10 non-MTBC mycobacteria and 4 bacteria not belonging to the genus Mycobacterium. All MTBC samples were successfully analyzed with the iPLEX assay, which yielded clear allelic data for 99.9% of the SNPs (879 out of 880). No false-positive results were obtained with the negative controls. Compared to the SNaPshot assay, the newly developed 16-plex iPLEX assay produced fully concordant results that allowed reliable differentiation of MTBC species and recognition of lineages, thus demonstrating its potential value in diagnostic, epidemiological, and evolutionary applications. Compared to the SNaPshot approach, the implementation of the iPLEX technology could offer a higher throughput and could be a more flexible and cost-effective option for microbiology laboratories.
本研究的主要目的是探讨一种新型的单核苷酸多态性(SNP)基因分型技术,即 iPLEX Gold(Sequenom),在同时分析 16 个 SNP 中的潜在用途,这些 SNP 已被证明可用于鉴定结核分枝杆菌复合群(MTBC)物种,并将 MTBC 分离株分为不同的遗传谱系,称为主要遗传群(PGG)和 SNP 簇群(SCG)。在这种情况下,我们基于等位基因特异性引物单碱基延伸反应,使用 iPLEX Gold 试剂盒(Sequenom)开发了一种 16 重 iPLEX 检测方法,然后在市售的 Sequenom MassARRAY 平台上进行基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)分析。该检测方法在 55 株经过充分特征描述的 MTBC 菌株的检测中进行了测试,这些菌株也使用先前报道的 SNaPshot 检测方法对相同的基因座进行了基因分型,此外还检测了 10 株非 MTBC 分枝杆菌和 4 株不属于分枝杆菌属的细菌。所有 MTBC 样本都成功地用 iPLEX 检测方法进行了分析,该方法对 99.9%(879 个中的 879 个)的 SNP 产生了清晰的等位基因数据。阴性对照未得到假阳性结果。与 SNaPshot 检测方法相比,新开发的 16 重 iPLEX 检测方法产生了完全一致的结果,可可靠地区分 MTBC 物种并识别谱系,从而证明了其在诊断、流行病学和进化应用中的潜在价值。与 SNaPshot 方法相比,iPLEX 技术的实施可能提供更高的通量,并且对于微生物学实验室来说可能是更灵活和更具成本效益的选择。