Reisig Florian, Kremer Kristin, Amthor Beate, van Soolingen Dick, Haas Walter H
Children's Hospital, University of Heidelberg, Heidelberg, Germany.
J Clin Microbiol. 2005 Nov;43(11):5622-7. doi: 10.1128/JCM.43.11.5622-5627.2005.
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.
IS6110限制性片段长度多态性(RFLP)分析是用于结核分枝杆菌复合群菌株分型的应用最为广泛的方法。我们之前描述过混合连接子PCR,这是一种基于IS6110的PCR方法,根据可重复性和区分菌株的能力,与其他用于结核分枝杆菌复合群的分型方法相比具有优势。在此我们报告该方法的进一步发展,即快速连接介导PCR(FLiP),它能够在一个工作日内,从少于1 ng的分枝杆菌DNA或粗细胞裂解物开始对菌株进行分析。对一组包含131株结核分枝杆菌复合群和非结核分枝杆菌分离株的标准菌株进行盲法分析,结果显示能够区分90株结核分枝杆菌复合群分离株中的81种类型,这些分离株具有84种不同的IS6110 RFLP指纹图谱,并且检测出了31个重复样本中的97%。我们认为,在开始高通量分析或标准IS6110 RFLP分析之前,FLiP可用于快速检测传播链。它也可以作为其他非基于IS6110的方法的二级分型技术。