Vandenbussche Frank, Lefebvre David J, De Leeuw Ilse, Van Borm Steven, De Clercq Kris
Molecular Platform, OD Viral Diseases, CODA-CERVA, Groeselenberg 99, 1180 Brussels, Belgium.
Service for Vesicular and Exotic Diseases, OD Viral Diseases, CODA-CERVA, Groeselenberg 99, 1180 Brussels, Belgium.
J Virol Methods. 2017 Aug;246:90-94. doi: 10.1016/j.jviromet.2017.04.014. Epub 2017 Apr 27.
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.
卡拉汉等人(2002年)和里德等人(2002年)的3D和5UTR实时逆转录聚合酶链反应检测法(RT-qPCR)是检测口蹄疫病毒(FMDV)常用的参考方法。为了在临床样本中实现对口蹄疫病毒的最佳检测,建议同时使用这两种检测方法(金等人,2006年)。最近,范登布舍等人(2016年)表明,在FMDV特异性引物上添加5'-尾可增强3D和5UTR RT-qPCR检测法中FMDV的检测效果。为了验证用于诊断目的的带有5'-尾引物的3D和5UTR RT-qPCR检测法,这两种检测法在一个以β-肌动蛋白作为内参、合成RNA作为外参的三重一步法RT-qPCR方案中平行进行。两种检测法均获得了低检测限、高线性度、高重复性和再现性、接近100%的分析特异性以及>99%的诊断准确性。得出的结论是,带有5'-尾引物的3D和5UTR RT-qPCR检测法特别适用于口蹄疫病毒的检测以及排除口蹄疫病毒的存在。