Eisenach K D, Crawford J T, Bates J H
Am Rev Respir Dis. 1986 Jun;133(6):1065-8. doi: 10.1164/arrd.1986.133.6.1065.
Chromosomal DNA isolated from 3 reference and 2 clinical isolates of Mycobacterium tuberculosis, 2 reference strains each of M. bovis and M. bovis BCG, and 1 reference strain of M. kansasii, was digested with 9 restriction endonucleases. The restriction fragments were analyzed by agarose gel electrophoresis. With each enzyme tested the patterns of the strains of M. tuberculosis, M. bovis, and M. bovis BCG were indistinguishable but clearly distinct from those of M. kansasii. A library of M. tuberculosis H37Rv DNA was prepared by cloning Bam HI digest fragments into lambda 1059. Eight randomly selected clones, having multiple Bam HI sites, were used to probe restriction digests of DNA from the strains of the tuberculosis complex. Two of the cloned segments hybridized with homologous fragments in 4 different enzyme digests of all strains. With 2 clones, hybridization differed among the strains; however, some homologous sequences were detected. With 4 clones, efficient hybridization occurred only with M. tuberculosis H37Rv DNA. These hybridization results indicate that some regions of the chromosome are highly conserved among members of the tuberculosis complex, whereas others are diverged. Selected DNA probes were useful in detecting differences among strains of the tuberculosis complex.
从3株结核分枝杆菌参考菌株和2株临床分离株、2株牛分枝杆菌参考菌株和2株卡介苗、以及1株堪萨斯分枝杆菌参考菌株中分离出的染色体DNA,用9种限制性内切酶进行消化。限制性片段通过琼脂糖凝胶电泳进行分析。在所测试的每种酶中,结核分枝杆菌、牛分枝杆菌和卡介苗菌株的图谱无法区分,但与堪萨斯分枝杆菌的图谱明显不同。通过将Bam HI消化片段克隆到λ1059中制备了结核分枝杆菌H37Rv DNA文库。八个随机选择的具有多个Bam HI位点的克隆用于探测结核分枝杆菌复合群菌株DNA的限制性消化产物。其中两个克隆片段在所有菌株的4种不同酶切消化产物中与同源片段杂交。对于另外两个克隆,各菌株之间的杂交情况有所不同;然而,仍检测到一些同源序列。对于另外4个克隆,仅与结核分枝杆菌H37Rv DNA发生有效杂交。这些杂交结果表明,染色体的某些区域在结核分枝杆菌复合群成员中高度保守,而其他区域则存在差异。所选的DNA探针可用于检测结核分枝杆菌复合群菌株之间的差异。