Oloya J, Opuda-Asibo J, Kazwala R, Demelash A B, Skjerve E, Lund A, Johansen T B, Djonne B
Department of Veterinary Public Health and Preventive Medicine, Makerere University, Kampala, Uganda.
Epidemiol Infect. 2008 May;136(5):636-43. doi: 10.1017/S0950268807009004. Epub 2007 Jun 29.
Mycobacteria from lymph node biopsies of patients with cervical lymphadenitis reporting for tuberculosis treatment in Matany and Moroto Hospitals in the transhumant areas of Karamoja, Uganda were isolated and characterized. The AccuProbe culture identification kits for Mycobacterium tuberculosis complex (MTC), M. avium complex (MAC) and M. avium were used to identify the isolates. Spoligotyping, IS901 PCR and IS1311 and IS1245 restriction fragment length polymorphism (RFLP) were used to characterize the isolates. Of the 43 biopsies, ten M. avium, seven M. tuberculosis, three M. bovis, and two M. intracellulare were isolated. Two isolates could not be identified with AccuProbe and from 19 samples no mycobacteria could be isolated. Three isolates with the Beijing spoligotype were identified from the seven M. tuberculosis isolates. The spoligopatterns of the M. bovis isolates had previously been detected in cattle in Uganda. Isolation of members of the MAC group reflects the complex interaction between the transhumant communities, water sources and their cattle. None of the M. avium isolates harboured IS901, and all showed several bands on IS1311 and IS1245 RFLP, in accordance with M. avium subsp. hominissuis. Composite dendrograms of IS1311 and IS1245 RFLP showed that the isolates were similar and identical patterns were found. The isolation of M. bovis confirms the human infection with zoonotic mycobacteria in areas where consumption of raw milk and meat is routine. Isolation of environmental mycobacteria also confirms their increasing role in human disease and the occupational risk of infection in the transhumant ecosystem in the absence of safe drinking water and environmental contamination.
对乌干达卡拉莫贾游牧地区马塔尼和莫罗托医院因结核病治疗前来就诊的颈淋巴结炎患者的淋巴结活检样本中的分枝杆菌进行了分离和鉴定。使用用于结核分枝杆菌复合群(MTC)、鸟分枝杆菌复合群(MAC)和鸟分枝杆菌的AccuProbe培养鉴定试剂盒对分离株进行鉴定。采用间隔寡核苷酸分型、IS901聚合酶链反应以及IS1311和IS1245限制性片段长度多态性(RFLP)对分离株进行特征分析。在43份活检样本中,分离出10株鸟分枝杆菌、7株结核分枝杆菌、3株牛分枝杆菌和2株胞内分枝杆菌。有2株分离株无法用AccuProbe鉴定,19份样本未分离出分枝杆菌。在7株结核分枝杆菌分离株中鉴定出3株具有北京间隔寡核苷酸分型。牛分枝杆菌分离株的间隔寡核苷酸分型模式此前在乌干达的牛中已被检测到。MAC组成员的分离反映了游牧社区、水源及其牛群之间复杂的相互作用。所有鸟分枝杆菌分离株均未携带IS901,并且在IS1311和IS1245 RFLP上均显示出多条条带,这与鸟分枝杆菌亚种人型相符。IS1311和IS1245 RFLP的复合树状图显示,分离株相似且发现了相同的模式。牛分枝杆菌的分离证实了在有饮用生奶和生肉习惯的地区存在人畜共患分枝杆菌的人类感染。环境分枝杆菌的分离也证实了它们在人类疾病中日益增加的作用以及在缺乏安全饮用水和环境污染的游牧生态系统中的职业感染风险。