Prodinger Wolfgang M, Brandstätter Anita, Naumann Ludmila, Pacciarini Maria, Kubica Tanja, Boschiroli Maria Laura, Aranaz Alicia, Nagy György, Cvetnic Zeljko, Ocepek Matjaz, Skrypnyk Artem, Erler Wilfried, Niemann Stefan, Pavlik Ivo, Moser Irmgard
Department of Hygiene, Microbiology, and Social Medicine, Innsbruck Medical University, Fritz Pregl-Strasse 3, A-6020 Innsbruck, Austria.
J Clin Microbiol. 2005 Oct;43(10):4984-92. doi: 10.1128/JCM.43.10.4984-4992.2005.
Mycobacterium caprae, a recently defined member of the Mycobacterium tuberculosis complex, causes tuberculosis among animals and, to a limited extent, in humans in several European countries. To characterize M. caprae in comparison with other Mycobacterium tuberculosis complex members and to evaluate genotyping methods for this species, we analyzed 232 M. caprae isolates by mycobacterial interspersed repetitive unit (MIRU) genotyping and by spoligotyping. The isolates originated from 128 distinct epidemiological settings in 10 countries, spanning a period of 25 years. We found 78 different MIRU patterns (53 unique types and 25 clusters with group sizes from 2 to 9) but only 17 spoligotypes, giving Hunter-Gaston discriminatory indices of 0.941 (MIRU typing) and 0.665 (spoligotyping). For a subset of 103 M. caprae isolates derived from outbreaks or endemic foci, MIRU genotyping and IS 6110 restriction fragment length polymorphism were compared and shown to provide similar results. MIRU loci 4, 26, and 31 were most discriminant in M. caprae, followed by loci 10 and 16, a combination which is different than those reported to discriminate M. bovis best. M. caprae MIRU patterns together with published data were used for phylogenetic inference analysis employing the neighbor-joining method. M. caprae isolates were grouped together, closely related to the branches of classical M. bovis, M. pinnipedii, M. microti, and ancestral M. tuberculosis, but apart from modern M. tuberculosis. The analysis did not reflect geographic patterns indicative of origin or spread of M. caprae. Altogether, our data confirm M. caprae as a distinct phylogenetic lineage within the Mycobacterium tuberculosis complex.
山羊分枝杆菌是结核分枝杆菌复合群中最近定义的一个成员,在几个欧洲国家会导致动物结核病,并在一定程度上导致人类结核病。为了将山羊分枝杆菌与其他结核分枝杆菌复合群成员进行比较并评估该菌种的基因分型方法,我们通过分枝杆菌散布重复单位(MIRU)基因分型和间隔寡核苷酸分型(spoligotyping)分析了232株山羊分枝杆菌分离株。这些分离株来自10个国家的128个不同的流行病学环境,时间跨度为25年。我们发现了78种不同的MIRU模式(53种独特类型和25个聚类,聚类大小从2到9),但只有17种间隔寡核苷酸分型,Hunter-Gaston鉴别指数分别为0.941(MIRU分型)和0.665(间隔寡核苷酸分型)。对于从疫情暴发或地方病疫源地获得的103株山羊分枝杆菌分离株的子集,比较了MIRU基因分型和IS 6110限制性片段长度多态性,结果显示二者提供了相似的结果。MIRU位点4、26和31在山羊分枝杆菌中鉴别力最强,其次是位点10和16,这种组合与据报道对牛分枝杆菌鉴别力最佳的组合不同。将山羊分枝杆菌的MIRU模式与已发表的数据一起用于采用邻接法的系统发育推断分析。山羊分枝杆菌分离株聚集在一起,与经典牛分枝杆菌、海豹分枝杆菌、田鼠分枝杆菌和祖先结核分枝杆菌的分支密切相关,但与现代结核分枝杆菌不同。该分析未反映出表明山羊分枝杆菌起源或传播的地理模式。总之,我们的数据证实山羊分枝杆菌是结核分枝杆菌复合群内一个独特的系统发育谱系。