Pérez-Martínez I, Ponce-De-León A, Bobadilla M, Villegas-Sepúlveda N, Pérez-García M, Sifuentes-Osornio J, González-y-Merchand J A, Estrada-García T
Department of Molecular Biomedicine, CINVESTAV-IPN, Zacatenco, Mexico City, Mexico.
Eur J Clin Microbiol Infect Dis. 2008 Jun;27(6):451-9. doi: 10.1007/s10096-008-0459-9. Epub 2008 Feb 2.
Recently, the incidence of human mycobacterial infections due to species other than M. tuberculosis has increased worldwide. Since disease control depends on appropriate antimicrobial therapy, the precise identification of these species of clinical importance has become a major public health concern. Identification of mycobacteria has been hampered because of the lack of specific, rapid, and inexpensive methods. Therefore, we aimed at designing and validating a bacterial lysate-based polymerase chain reaction identification scheme. This scheme can classify clinical isolates into: (1) the genus Mycobacterium, (2) the M. tuberculosis complex, (3) the nontuberculous mycobacteria, and (4) the species M. avium, M. intracellulare, M. abscessus, M. chelonae, M. fortuitum and M. bovis of clinical importance, and M. gordonae, the most commonly encountered nonpathogenic species in clinical laboratories. By using M. fortuitum and M. avium lysates as models, the method sensitivity was determined to be 372 pg of DNA. In a blind parallel comparison between our approach and conventional biochemical tests, both assays correctly categorized 75 patient's mycobacterial isolates. However, our approach only required 4-9 h for categorization compared with at least 15 days by conventional tests. Furthermore, our methodology could also detect M. fortuitum and M. avium from liquid cultures, after only 2 and 6 days, respectively, of incubation. Our new identification scheme is therefore sensitive, specific, rapid, and economic. Additionally, it can help to provide proper treatment to patients, to control these diseases, and to improve our knowledge of the epidemiology of mycobacteriosis, all urgently needed, particularly in developing countries.
近年来,全球范围内由结核分枝杆菌以外的其他分枝杆菌引起的人类分枝杆菌感染发病率有所上升。由于疾病控制依赖于适当的抗菌治疗,准确鉴定这些具有临床重要性的分枝杆菌种类已成为一个主要的公共卫生问题。由于缺乏特异性、快速且廉价的方法,分枝杆菌的鉴定一直受到阻碍。因此,我们旨在设计并验证一种基于细菌裂解物的聚合酶链反应鉴定方案。该方案可将临床分离株分为:(1)分枝杆菌属;(2)结核分枝杆菌复合群;(3)非结核分枝杆菌;(4)具有临床重要性的鸟分枝杆菌、胞内分枝杆菌、脓肿分枝杆菌、龟分枝杆菌、偶然分枝杆菌和牛分枝杆菌种,以及戈登分枝杆菌,它是临床实验室中最常见的非致病菌种。以偶然分枝杆菌和鸟分枝杆菌裂解物为模型,确定该方法的灵敏度为372 pg DNA。在我们的方法与传统生化试验的盲法平行比较中,两种检测方法都正确地对75例患者的分枝杆菌分离株进行了分类。然而,我们的方法分类仅需4 - 9小时,而传统试验至少需要15天。此外,我们的方法分别在培养2天和6天后,也能从液体培养物中检测出偶然分枝杆菌和鸟分枝杆菌。因此,我们的新鉴定方案灵敏、特异、快速且经济。此外,它有助于为患者提供适当的治疗,控制这些疾病,并增进我们对分枝杆菌病流行病学的了解,这些都是迫切需要的,特别是在发展中国家。