Wiid I J, Werely C, Beyers N, Donald P, van Helden P D
Department of Medical Biochemistry, University of Stellenbosch, Tygerberg, Republic of South Africa.
J Clin Microbiol. 1994 May;32(5):1318-21. doi: 10.1128/jcm.32.5.1318-1321.1994.
Culture of Mycobacterium tuberculosis provides no information on the identity of a strain or the distribution of such a strain in the community. Strain identification of M. tuberculosis can help to address important epidemiological questions, e.g., the origin of an infection in a patient's household or community, whether reactivation of infection is endogenous or exogenous in origin, and the spread and early detection of organisms with acquired antibiotic resistance. To research this problem, strain identification must be reliable and accurate. Although genetic identification techniques already exist, it is valuable to have genetic identification techniques based on a number of genetic markers to improve the accurate identification of M. tuberculosis strains. We show that oligonucleotide (GTG)5 can be successfully applied to the identification of M. tuberculosis strains. This technique may be particularly useful in cases in which M. tuberculosis strains have few or no insertion elements (e.g., IS6110) or in identifying other strains of mycobacteria when informative probes are lacking.
结核分枝杆菌培养无法提供有关菌株身份或该菌株在社区中分布情况的信息。结核分枝杆菌的菌株鉴定有助于解决重要的流行病学问题,例如患者家庭或社区中感染的来源、感染的再激活是内源性还是外源性的,以及获得性抗生素耐药性生物体的传播和早期检测。为了研究这个问题,菌株鉴定必须可靠且准确。尽管已经存在基因鉴定技术,但拥有基于多种遗传标记的基因鉴定技术对于提高结核分枝杆菌菌株的准确鉴定很有价值。我们表明,寡核苷酸(GTG)5可成功应用于结核分枝杆菌菌株的鉴定。该技术在结核分枝杆菌菌株插入元件很少或没有(例如IS6110)的情况下,或在缺乏信息性探针时鉴定其他分枝杆菌菌株时可能特别有用。