Bonora S, Gutierrez M C, Di Perri G, Brunello F, Allegranzi B, Ligozzi M, Fontana R, Concia E, Vincent V
Institute of Immunology and Infectious Diseases, University of Verona, 37126 Verona, Italy.
J Clin Microbiol. 1999 Oct;37(10):3118-23. doi: 10.1128/JCM.37.10.3118-3123.1999.
Spoligotyping has been suggested as a screening test in multistep genotyping of Mycobacterium tuberculosis strains. Relying on restriction fragment length polymorphism (RFLP) analysis with IS6110 (IS6110 RFLP analysis) as a "gold standard," we performed a comparative evaluation of spoligotyping and ligation-mediated PCR (LMPCR), a recently described PCR-based typing method, as rapid screening tests for fingerprinting of 158 M. tuberculosis strains collected in Verona, Italy. LMPCR seemed to be comparable to spoligotyping in terms both of feasibility with rapidly extracted DNA and of generation of software-analyzable images. Moreover, LMPCR grouped considerably fewer strains than spoligotyping (38 versus 67%) and was found to reduce the cluster overestimation rate (26.3 versus 58%) and to give a better discriminatory index (0.992 versus 0.970) compared to spoligotyping. In our geographical region, where there was no evidence of clustered strains carrying fewer than six IS6110 copies, LMPCR was found to be more discriminatory than spoligotyping. We also evaluated two models of three-step typing strategies, involving the use of spoligotyping and LMPCR as screening methods and IS6110 RFLP analysis as a further supporting test. LMPCR proved to be a more effective first-step test than spoligotyping, significantly reducing the need for subtyping. LMPCR should be considered an alternative to spoligotyping as a rapid screening method for M. tuberculosis fingerprinting, particularly in areas with a low prevalence of M. tuberculosis strains carrying few copies of IS6110.
spoligotyping已被建议作为结核分枝杆菌菌株多步骤基因分型中的一种筛查试验。以IS6110限制性片段长度多态性(RFLP)分析(IS6110 RFLP分析)作为“金标准”,我们对spoligotyping和连接介导的PCR(LMPCR,一种最近描述的基于PCR的分型方法)进行了比较评估,将其作为对在意大利维罗纳收集的158株结核分枝杆菌菌株进行指纹识别的快速筛查试验。LMPCR在使用快速提取的DNA的可行性以及生成软件可分析图像方面似乎与spoligotyping相当。此外,与spoligotyping相比,LMPCR分组的菌株数量要少得多(38%对67%),并且发现其降低了聚类高估率(26.3%对58%),并给出了更好的鉴别指数(0.992对0.970)。在我们所在的地理区域,没有证据表明携带少于六个IS6110拷贝的菌株存在聚类情况,发现LMPCR比spoligotyping更具鉴别力。我们还评估了两种三步分型策略模型,包括使用spoligotyping和LMPCR作为筛查方法,以及IS6110 RFLP分析作为进一步的支持试验。事实证明,LMPCR作为第一步试验比spoligotyping更有效,显著减少了亚型分型的需求。LMPCR应被视为spoligotyping的替代方法,作为结核分枝杆菌指纹识别的快速筛查方法,特别是在携带少量IS6110拷贝的结核分枝杆菌菌株患病率较低的地区。