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Evaluation of a TaqMan real-time PCR for the detection of Theileria parva in buffalo and cattle

机译:TaqMan实时荧光定量PCR检测水牛和牛中泰勒菌的评估

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A real-time PCR assay based on TaqMan probe chemistry was developed for the detection of Theileria parva DNA in blood samples. It uses a Theileria genus-specific PCR primer set and a T. parva-specific probe to amplify and hybridize with a species-specific part of the 18S rRNA gene of the parasite. The test was evaluated using positive and negative reference blood samples and shown to be specific for T. parva. Analytical sensitivity was determined by testing a dilution series of T. parva positive blood. It was shown to be able to detect parasitaemia as low as 2 x 10(-6)%. The Taqman assay results were also compared with that obtained with the real-time hybridization probe PCR assay, which is currently employed as the official test for the diagnosis of T. parva infections in buffalo and cattle and was shown to be equally sensitive. A panel of 1164 field samples was screened using both assays and 164 samples tested positive in both tests, indicating a good correlation
机译:开发了一种基于TaqMan探针化学的实时PCR检测试剂盒,用于检测血液样本中的泰勒菌小虫DNA。它使用Theileria属特异性PCR引物组和T. parva特异性探针扩增该寄生虫的18S rRNA基因的物种特异性部分并与之杂交。使用阳性和阴性参比血液样品对测试进行评估,并显示其对丁香分枝杆菌具有特异性。分析敏感性是通过测试稀释的T. parva阳性血液系列来确定的。它被证明能够检测低至2 x 10(-6)%的寄生虫血症。 Taqman分析的结果也与实时杂交探针PCR分析的结果进行了比较,实时杂交探针PCR分析目前被用作诊断水牛和牛T. parva感染的官方检测方法,并且显示出同样的敏感性。使用这两种检测方法筛选了一组1164个现场样品,并且在两个测试中检测出164个样品均为阳性,表明相关性良好

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