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Fast Ligation-Mediated PCR, a Fast and Reliable Method for IS6110-Based Typing of Mycobacterium tuberculosis Complex

机译:快速连接介导的PCR,一种基于IS6110的结核分枝杆菌复合体快速,可靠的分型方法

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摘要

IS6110 restriction fragment length polymorphism (RFLP) analysis is the most widely applied method for strain differentiation of Mycobacterium tuberculosis complex. We have previously described mixed-linker PCR, an IS6110-based PCR method that favorably compared with other typing methods for M. tuberculosis complex according to reproducibility and ability to differentiate between strains. Here we report the further development of this method, called fast ligation-mediated PCR (FLiP), which allows analysis of strains within one working day and starting from less than 1 ng of mycobacterial DNA or a crude cell lysate. Blinded analysis of a standard set of 131 M. tuberculosis complex and nontuberculous isolates showed the ability to differentiate 81 types among 90 M. tuberculosis complex isolates with 84 different IS6110 RFLP fingerprint patterns and detected 97% of the 31 duplicate samples. We suggest that FLiP can serve to rapidly detect chains of transmission prior to starting high-throughput analysis or standard IS6110 RFLP. It may as well serve as a secondary typing technique for other, non-IS6110-based methods.
机译:IS6110限制性片段长度多态性(RFLP)分析是结核分枝杆菌复合体菌株分化最广泛的方法。我们先前已经描述了混合接头PCR,这是一种基于IS6110的PCR方法,根据其可复制性和区分菌株的能力,可以与其他结核分枝杆菌复合体分型方法相比更好地进行比较。在这里,我们报道了这种方法的进一步发展,称为快速连接介导的PCR(FLiP),它允许在一个工作日内分析菌株,并且从少于1 ng的分枝杆菌DNA或粗细胞裂解液开始。对一组标准的131 M.结核复合体和非结核分离株的盲法分析显示,能够在84种IS6110 RFLP指纹图谱中区分90 M.结核复合体中的81种类型,并检测出31个重复样品中的97%。我们建议FLiP可用于在开始高通量分析或标准IS6110 RFLP之前快速检测传输链。它也可以用作其他非基于IS6110的方法的辅助键入技术。

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