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Molecular diagnosis of Anaplasma marginale in cattle: quantitative evaluation of a real-time PCR (Polymerase Chain Reaction) based on msp5 gene

机译:牛边缘无浆体的分子诊断:基于msp5基因的实时PCR(聚合酶链反应)的定量评估

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The rickettsia Anaplasma marginale is considered the main agent of bovine anaplasmosis. Due the nonspecific clinical signs of the anaplasmosis, the diagnosis of infection depends of laboratory confirmation. In recent years, molecular diagnostic methods have been used to detect A. marginale in cattle. However, the existence of a large number of assays of different sensitivity and cost makes the choice of an appropriate test difficult. In the present study, a real-time Polymerase Chain Reaction (PCR) based on the msp5 target gene was quantitatively assessed and compared to an end point PCR. Both reactions were subjected to sensitivity and specificity evaluation using plasmid DNA and samples from cattle experimentally infected with A. marginale. A comparative field trial of the tests was carried out using samples of cattle from a stable enzootic area for A. marginale. The real-time PCR showed a higher sensitivity than the end point PCR. This reaction (i.e. real-time PCR) was able to detect one copy of the msp5 gene in 100 ηg of plasmidial DNA, and more than 80% of its results were positive among experimentally infected animals seven days after infection. In addition, based on in silico analysis, the real-time PCR evaluated in the present study appears to be useful for the detection of A. ovis.
机译:立克次氏体无浆膜被认为是牛无形体病的主要病原体。由于无特异性的临床症状,感染的诊断取决于实验室的确认。近年来,已经使用分子诊断方法来检测牛中的拟南芥。但是,由于存在大量灵敏度和成本不同的分析方法,因此很难选择合适的测试方法。在本研究中,定量评估了基于msp5目标基因的实时聚合酶链反应(PCR),并将其与终点PCR进行了比较。两种反应均使用质粒DNA和实验性感染了拟南芥的牛的样品进行敏感性和特异性评估。使用来自稳定的盲肠地区的牛的样本进行了比较试验。实时PCR显示出比终点PCR更高的灵敏度。该反应(即实时PCR)能够在100ηg质粒DNA中检测到msp5基因的一个拷贝,感染后7天,实验感染的动物中80%以上的结果均为阳性。此外,基于计算机分析,在本研究中评估的实时PCR似乎对检测A. ovis有用。

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