Collins D M, De Lisle G W
J Gen Microbiol. 1984 Apr;130(4):1019-21. doi: 10.1099/00221287-130-4-1019.
DNA preparations from two reference (H37Ra and H37Rv) and two wild strains of Mycobacterium tuberculosis and one re-isolated strain of Mycobacterium bovis BCG were analysed using 17 restriction endonucleases. The enzyme BstEII revealed the greatest differences between strains. Electrophoretic DNA patterns from the wild M. tuberculosis strains differed from each other and from the reference strains at relatively few positions. At the highest resolution attained, patterns from the two reference strains remained indistinguishable from each other. The pattern of the M. bovis BCG strain was substantially different from, but had many bands in common with, the M. tuberculosis patterns.
使用17种限制性内切酶对来自两种参考菌株(H37Ra和H37Rv)、两种结核分枝杆菌野生菌株以及一株牛分枝杆菌卡介苗重分离菌株的DNA制剂进行了分析。BstEII酶揭示了菌株之间最大的差异。野生结核分枝杆菌菌株的电泳DNA图谱彼此之间以及与参考菌株相比,在相对较少的位置存在差异。在获得的最高分辨率下,两种参考菌株的图谱彼此无法区分。牛分枝杆菌卡介苗菌株的图谱与结核分枝杆菌的图谱有很大不同,但有许多条带是共有的。