Telenti A, Marchesi F, Balz M, Bally F, Böttger E C, Bodmer T
Institut für Medizinische Mikrobiologie, Universität Bern, Switzerland.
J Clin Microbiol. 1993 Feb;31(2):175-8. doi: 10.1128/jcm.31.2.175-178.1993.
A method for the rapid identification of mycobacteria to the species level was developed on the basis of evaluation by the polymerase chain reaction (PCR) of the gene encoding for the 65-kDa protein. The method involves restriction enzyme analysis of PCR products obtained with primers common to all mycobacteria. Using two restriction enzymes, BstEII and HaeIII, medically relevant and other frequent laboratory isolates were differentiated to the species or subspecies level by PCR-restriction enzyme pattern analysis. PCR-restriction enzyme pattern analysis was performed on isolates (n = 330) from solid and fluid culture media, including BACTEC, or from frozen and lyophilized stocks. The procedure does not involve hybridization steps or the use of radioactivity and can be completed within 1 working day.
基于对编码65 kDa蛋白的基因进行聚合酶链反应(PCR)评估,开发了一种将分枝杆菌快速鉴定到种水平的方法。该方法包括对用所有分枝杆菌通用引物获得的PCR产物进行限制性酶切分析。使用两种限制性酶BstEII和HaeIII,通过PCR-限制性酶切图谱分析将医学相关的和其他常见的实验室分离株区分到种或亚种水平。对来自固体和液体培养基(包括BACTEC)或冷冻和冻干菌库的分离株(n = 330)进行了PCR-限制性酶切图谱分析。该程序不涉及杂交步骤或放射性的使用,并且可以在1个工作日内完成。