Haas W H, Bretzel G, Amthor B, Schilke K, Krommes G, Rüsch-Gerdes S, Sticht-Groh V, Bremer H J
Department of General Pediatrics, Children's Hospital, Heidelberg University, Germany.
J Clin Microbiol. 1997 Mar;35(3):663-6. doi: 10.1128/jcm.35.3.663-666.1997.
Mycobacterium africanum is a pathogen found in tuberculosis patients in certain parts of Africa and is a member of the Mycobacterium tuberculosis complex. Biochemically, strains of M. africanum exhibit a high degree of variability, with some tendency to cluster according to their geographical origin. To investigate whether this phenotypic variability is reflected at the genetic level, we performed DNA fingerprint analysis of strains isolated from patients with pulmonary tuberculosis in Uganda and Sierra Leone. IS6110 DNA fingerprinting was carried out by the mixed-linker PCR method. A total of 138 strains of M. africanum were analyzed: 42 isolates from Uganda and 96 isolates from Sierra Leone. With few exceptions, the resulting DNA fingerprint patterns grouped together according to their country of origin. A striking lack of variability of DNA fingerprints was found for strains from Sierra Leone, where 70 of 96 isolates (61.5%) fell into clusters. The two largest clusters accounted for 41.7% of all isolates and differed by only one band, as confirmed by standard DNA fingerprinting. In contrast, only two clusters (7.1%) with two and three isolates, respectively, were found for M. africanum isolates collected in Uganda, and three of the DNA fingerprints contained fewer than seven bands. Strains of M. tuberculosis collected and processed during the same time period were highly variable in both countries. Our results support the concept of geographically defined subtypes of M. africanum. In addition, they demonstrate that natural geographic differences in the variability of IS6110 DNA fingerprints within the M. tuberculosis complex must be considered if this technique is used for epidemiologic studies.
非洲分枝杆菌是在非洲某些地区的结核病患者中发现的一种病原体,属于结核分枝杆菌复合群。从生化角度来看,非洲分枝杆菌菌株表现出高度的变异性,并且有根据地理来源聚类的趋势。为了研究这种表型变异性是否在基因水平上有所体现,我们对从乌干达和塞拉利昂的肺结核患者中分离出的菌株进行了DNA指纹分析。采用混合接头PCR方法进行IS6110 DNA指纹分析。共分析了138株非洲分枝杆菌菌株:42株来自乌干达的分离株和96株来自塞拉利昂的分离株。除少数例外,所得的DNA指纹图谱根据其原产国聚集在一起。在塞拉利昂的菌株中发现DNA指纹缺乏明显变异性,96株分离株中有70株(61.5%)聚为簇。通过标准DNA指纹分析证实,两个最大的簇占所有分离株的41.7%,且仅相差一条带。相比之下,在乌干达收集的非洲分枝杆菌分离株中仅发现两个簇(7.1%),分别包含两株和三株分离株,并且三个DNA指纹包含的条带少于七条。在同一时期收集和处理的结核分枝杆菌菌株在这两个国家都具有高度变异性。我们的结果支持非洲分枝杆菌存在地理定义亚型的概念。此外,它们表明,如果将该技术用于流行病学研究,必须考虑结核分枝杆菌复合群内IS6110 DNA指纹变异性的自然地理差异。