Brunello F, Ligozzi M, Cristelli E, Bonora S, Tortoli E, Fontana R
Dipartimento di Patologia, Sezione di Microbiologia, Università di Verona, Italy.
J Clin Microbiol. 2001 Aug;39(8):2799-806. doi: 10.1128/JCM.39.8.2799-2806.2001.
A total of 121 reference and clinical strains of both slowly and rapidly growing mycobacteria belonging to 54 species were studied for restriction fragment length polymorphism of a PCR-amplified 439-bp segment of the gene encoding the 65-kDa heat shock protein. Restriction digests were separated by 10% polyacrylamide gel electrophoresis (PAGE). By including a size standard in each sample, the restriction fragment profile was calculated using a computer-aided comparison program. An algorithm describing these 54 species (including 22 species not previously described) is proposed. We found that this assay based on 10% PAGE provided a more precise estimate than that based on agarose gel electrophoresis of the real size of restriction fragments as deduced from the sequence analysis and allowed identification of mycobacteria whose PCR-restriction fragment length polymorphism analysis patterns were unequivocally identified by fragments shorter than 60 bp.
对总共121株属于54个种的缓慢生长和快速生长分枝杆菌的参考菌株和临床菌株,研究了编码65 kDa热休克蛋白的基因经聚合酶链反应(PCR)扩增的439 bp片段的限制性片段长度多态性。限制性酶切产物通过10%聚丙烯酰胺凝胶电泳(PAGE)进行分离。通过在每个样品中加入一个大小标准物,使用计算机辅助比较程序计算限制性片段图谱。提出了一种描述这54个种(包括22个以前未描述的种)的算法。我们发现,基于10% PAGE的该检测方法比基于琼脂糖凝胶电泳的方法能更精确地估计从序列分析推断的限制性片段的实际大小,并且能够鉴定出其PCR-限制性片段长度多态性分析模式可通过短于60 bp的片段明确鉴定的分枝杆菌。