首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >Detection of viable Mycobacterium leprae in soil samples: Insights into possible sources of transmission of leprosy.
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Detection of viable Mycobacterium leprae in soil samples: Insights into possible sources of transmission of leprosy.

机译:检测土壤样品中活的麻风分枝杆菌:深入了解麻风传播的可能来源。

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Leprosy has ceased to be a public health problem world wide, after the successful implementation of effective chemotherapy (MDT) and use of control measures. However, new cases of leprosy continue to occur. Mycobacterium leprae cannot be grown in any acceptable culture medium and besides the wild armadillos, there is no known animal reservoir for leprosy. The transmission of leprosy is believed to be due to a large extent by droplet discharge of bacilli through nose and mouth and to a lesser extent by direct contact of susceptible host with a patient for long duration. The exact role of the environment in the transmission dynamics is still speculative. In the present study, we have tried to detect viable M. leprae from soil samples in endemic areas by using molecular methods. Eighty soil samples were collected from villages of this area, DNA and RNA of M. leprae extracted and identified using specific M. leprae primers. PCR amplification was done and real-time RT-PCR was used to detect viable M. leprae. DNA targeting the 16S region of M. leprae was detected in 37.5%, whereas M. leprae RNA targeting the same region was detected in 35% of these samples. Of the total 80 samples, 40 were collected from residential areas of leprosy patients whereas 40 samples were from no-patient areas. Fifty-five percent positivity for 16S rRNA of M. leprae was observed from the "patient" area in comparison to 15% positivity from the "no-patient" area (p<0.001). This study thus provides valuable information of presence of viable M. leprae in soil specimens, which would be of use in investigating the transmission dynamics in leprosy.
机译:在成功实施有效的化学疗法(MDT)和采取控制措施之后,麻风病已不再是全世界的公共卫生问题。但是,新的麻风病病例继续发生。麻风分枝杆菌不能在任何可接受的培养基中生长,除了野生犰狳以外,没有已知的麻风病动物库。麻风病的传播被认为是由于细菌通过鼻和口的小滴排出而引起的,而在较小程度上是由于易感宿主与患者长时间的直接接触所致。环境在传动动力学中的确切作用仍是推测性的。在本研究中,我们试图通过分子方法从流行地区的土壤样品中检测出活的麻风杆菌。从该地区的村庄中收集了80个土壤样品,提取了麻风分枝杆菌的DNA和RNA,并使用特异的麻风分枝杆菌引物进行了鉴定。进行PCR扩增,并使用实时RT-PCR检测活的麻风分支杆菌。在这些样品中有35%检测到了针对麻风分枝杆菌16S区域的DNA,而在同一样本中检测到了针对相同区域的麻风分枝杆菌RNA。在总共80个样本中,有40个样本来自麻风病人的居住区,而40个样本来自非病人区域。从“患者”区域观察到麻风分枝杆菌16S rRNA的阳性率为55%,而从“非患者”区域观察到阳性率为15%(p <0.001)。因此,这项研究提供了有价值的信息,表明土壤标本中存在活的麻风分枝杆菌,这可用于研究麻风病的传播动态。

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