Yang M, Ross B C, Dwyer B
Infectious Diseases Department, First Affiliated Hospital, Suzhou Medical College, People's Republic of China.
J Clin Microbiol. 1993 Oct;31(10):2769-72. doi: 10.1128/jcm.31.10.2769-2772.1993.
In order to develop a DNA-based assay to identify all Mycobacterium kansasii clinical isolates, a specific DNA probe was isolated in plasmid p6123. A total of 145 M. kansasii clinical isolates were collected from several countries and were examined with three probes by DNA hybridization. Of the 145 isolates, 115 (79%) were positive with the previously described probe pMK1-9 (Z. H. Huang, B. C. Ross, and B. Dwyer, J. Clin. Microbiol. 29:2125-2129, 1991), 129 (88%) were positive with the commercial Accu-probe assay (Gen-Probe), and 145 (100%) were positive with the p6123 probe. Southern blot analysis of EcoRI-digested M. kansasii chromosomal DNA with p6123 revealed that all Accu-probe-positive M. kansasii strains exhibited a 3-kb fragment, whereas all Accu-probe-negative M. kansasii strains displayed DNA fragments of variable molecular sizes. These results indicate that, unlike the previously described probes for M. kansasii, the fragment cloned into p6123 identified all 145 biochemically typical strains tested and provides an ideal target for future DNA-based speciation assays.
为了开发一种基于DNA的检测方法来鉴定所有堪萨斯分枝杆菌临床分离株,在质粒p6123中分离出一种特异性DNA探针。从几个国家收集了总共145株堪萨斯分枝杆菌临床分离株,并通过DNA杂交用三种探针进行检测。在这145株分离株中,115株(79%)对先前描述的探针pMK1-9呈阳性(Z. H. Huang、B. C. Ross和B. Dwyer,《临床微生物学杂志》29:2125-2129,1991年),129株(88%)对商业Accu-probe检测法(Gen-Probe)呈阳性,145株(100%)对p6123探针呈阳性。用p6123对经EcoRI消化的堪萨斯分枝杆菌染色体DNA进行Southern印迹分析表明,所有Accu-probe阳性的堪萨斯分枝杆菌菌株均显示出一条3 kb的片段,而所有Accu-probe阴性的堪萨斯分枝杆菌菌株则显示出分子大小可变的DNA片段。这些结果表明,与先前描述的堪萨斯分枝杆菌探针不同,克隆到p6123中的片段鉴定了所检测的所有145株生化典型菌株,并为未来基于DNA的物种鉴定检测提供了理想的靶标。