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Evaluation of Molecular Methods To Improve the Detection of Burkholderia pseudomallei in Soil and Water Samples from Laos

机译:评价改进老挝土壤和水样中伯克霍尔德氏菌检测方法的分子方法

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Burkholderia pseudomallei is the cause of melioidosis, a severe and potentially fatal disease of humans and animals. It is endemic in northern Australia and Southeast Asia and is found in soil and surface water. The environmental distribution of B. pseudomallei worldwide and within countries where it is endemic, such as the Lao People's Democratic Republic (Laos), remains unclear. However, this knowledge is important to our understanding of the ecology and epidemiology of B. pseudomallei and to facilitate public health interventions. Sensitive and specific methods to detect B. pseudomallei in environmental samples are therefore needed. The aim of this study was to compare molecular and culture-based methods for the detection of B. pseudomallei in soil and surface water in order to identify the optimal approach for future environmental studies in Laos. Molecular detection by quantitative real-time PCR (qPCR) was attempted after DNA extraction directly from soil or water samples or after an overnight enrichment step. The positivity rates obtained by qPCR were compared to those obtained by different culture techniques. The rate of detection from soil samples by qPCR following culture enrichment was significantly higher (84/100) than that by individual culture methods and all culture methods combined (44/100; P < 0.001). Similarly, qPCR following enrichment was the most sensitive method for filtered river water compared with the sensitivity of the individual methods and all individual methods combined. In conclusion, molecular detection following an enrichment step has proven to be a sensitive and reliable approach for B. pseudomallei detection in Lao environmental samples and is recommended as the preferred method for future surveys.
机译:假伯克霍尔德氏菌是类人猿病的病因,后者是人类和动物的一种严重且可能致命的疾病。它在澳大利亚北部和东南亚地区很流行,存在于土壤和地表水中。目前尚不清楚在世界范围内以及在地方病流行地区(例如老挝人民民主共和国(老挝))内的假疟原虫的环境分布。但是,这些知识对于我们对假单胞菌的生态学和流行病学的理解以及促进公共卫生干预非常重要。因此,需要灵敏且特定的方法来检测环境样品中的假疟原虫。这项研究的目的是比较基于分子和培养的方法来检测土壤和地表水中的假苹果芽孢杆菌,以便为今后在老挝的环境研究确定最佳方法。直接从土壤或水样中提取DNA或过夜富集步骤后,尝试通过定量实时PCR(qPCR)进行分子检测。将通过qPCR获得的阳性率与通过不同培养技术获得的阳性率进行比较。培养富集后通过qPCR从土壤样品中检出的比率(84/100)明显高于单个培养方法和所有培养方法的结合检出率(44/100; P <0.001)。同样,与单独方法和所有单独方法的敏感性相比,富集后的qPCR是过滤河水最敏感的方法。总之,富集步骤后的分子检测已被证明是老挝环境样品中假双歧杆菌检测的灵敏和可靠方法,并被推荐作为未来调查的首选方法。

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