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首页> 外文期刊>Journal of Virological Methods >Laboratory validation of two real-time RT-PCR methods with 5 '-tailed primers for an enhanced detection of foot-and-mouth disease virus
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Laboratory validation of two real-time RT-PCR methods with 5 '-tailed primers for an enhanced detection of foot-and-mouth disease virus

机译:两种实时RT-PCR方法的实验室验证,具有5'型引物,用于增强脚口病病毒的检测

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The 3D and 5UTR real-time RT-PCR assays (RT-qPCR) from Callahan et al. (2002) and Reid et al. (2002) are commonly used reference methods for the detection of foot-and-mouth disease virus (FMDV). For an optimal detection of FMDV in clinical samples, it is advised to use both assays simultaneously (King et al., 2006). Recently, Vandenbussche et al. (2016) showed that the addition of 5 '-tails to the FMDV-specific primers enhances the detection of FMDV in both the 3D and the 5UTR RT-qPCR assay. To validate the 3D and 5UTR RT-qPCR assays with 5 '-tailed primers for diagnostic purposes, both assays were run in parallel in a triplex one-step RT-qPCR protocol with beta-actin as an internal control and synthetic RNA as an external control. We obtained low limits of detection and high linearity's, high repeatability and reproducibility, near 100% analytical specificity and > 99% diagnostic accuracy for both assays. It was concluded that the 3D and 5UTR RT-qPCR assays with 5 '-tailed primers are particularly suited for the detection of FMDV as well as to exclude the presence of FMDV.
机译:来自Callahan等人的3D和5UTR实时RT-PCR测定(RT-QPCR)。 (2002)和Reid等人。 (2002)是常用的参考方法,用于检测口蹄疫病毒(FMDV)。为了在临床样本中最佳地检测FMDV,建议使用两种测定(King等,2006)。最近,Vandenbussche等。 (2016)表明,向FMDV特异性引物加入5' - Tails增强了3D和5UTR RT-QPCR测定中FMDV的检测。为了验证3D和5UTR RTR-QPCR测定的5'TaILed引物进行诊断目的,两种测定在三重单步RT-QPCR方案中并联运行,β-肌动蛋白是作为外部的内部控制和合成RNA控制。我们获得了低限制的检测和高线性度,高可重复性和再现性,接近100%的分析特异性和两个测定的诊断精度> 99%。得出结论是,用5' - 标记引物的3D和5UTR RT-QPCR测定特别适用于检测FMDV,以及排除FMDV的存在。

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