Thierry D, Vincent V, Clément F, Guesdon J L
Laboratoire de Prédéveloppement des Sondes, Institut Pasteur, Paris, France.
J Clin Microbiol. 1993 May;31(5):1048-54. doi: 10.1128/jcm.31.5.1048-1054.1993.
We cloned and sequenced two DNA fragments (DT1 and DT6) from Mycobacterium avium serotype 2 for use in the identification of members of the M. avium-M. intracellulare complex (MAC). Reference strains of MAC belonging to serovars 1 to 28 were examined by using these DNA fragments as probes. The study revealed that the DT6 probe hybridized with DNAs from M. avium strains (serovars 1 to 6, 8 to 11, and 21), while the DT1 probe hybridized with DNAs from serovars 2, 3, 7, 12 to 20, and 23 to 25. DT1- and DT6-derived oligonucleotides were selected for use as primers in a polymerase chain reaction test. Amplification of the DT1 and DT6 sequences may provide the basis for a rapid and reliable assay for the detection of mycobacteria belonging to MAC.
我们从鸟分枝杆菌血清型2中克隆并测序了两个DNA片段(DT1和DT6),用于鉴定鸟分枝杆菌-胞内分枝杆菌复合体(MAC)的成员。使用这些DNA片段作为探针,对属于血清型1至28的MAC参考菌株进行了检测。研究表明,DT6探针与鸟分枝杆菌菌株(血清型1至6、8至11和21)的DNA杂交,而DT1探针与血清型2、3、7、12至20以及23至25的DNA杂交。选择源自DT1和DT6的寡核苷酸用作聚合酶链反应试验的引物。DT1和DT6序列的扩增可为快速可靠地检测属于MAC的分枝杆菌提供基础。