Peiman M, Xie C
Key Laboratory of Horticultural Plant Biology, Huazhong Agricultural University, Wuhan, PR China.
Acta Virol. 2006;50(2):129-33.
A multiplex RT-PCR (mRT-PCR) for detecting four potato viruses (Potato virus S (PVS), Potato virus X (PVX), Potato virus Y (PVY), and Potato leaf roll virus (PLRV)) and one potato viroid (Potato spindle tuber viroid (PSTVd)) was developed. The mRT-PCR consisted of one reaction with specific primers designed according to the sequences of coat protein (CP) genes of respective viruses and the sequence of the viroid. The entire procedure from tissue grinding to RT-PCR results takes about 4 hrs. The reliability of the method was tested on leaves sampled from the field, greenhouse and in vitro-grown plants by comparison with double-antibody sandwich ELISA (DAS-ELISA). A high correlation between these two methods was observed. The mRT-PCR was also evaluated by testing infected samples obtained from the International Potato Center, Lima, Peru; this testing confirmed its high reliability and sensitivity.
开发了一种用于检测四种马铃薯病毒(马铃薯S病毒(PVS)、马铃薯X病毒(PVX)、马铃薯Y病毒(PVY)和马铃薯卷叶病毒(PLRV))和一种马铃薯类病毒(马铃薯纺锤块茎类病毒(PSTVd))的多重逆转录聚合酶链反应(mRT-PCR)。mRT-PCR由一个反应组成,该反应使用根据各病毒外壳蛋白(CP)基因序列和类病毒序列设计的特异性引物。从组织研磨到RT-PCR结果的整个过程大约需要4小时。通过与双抗体夹心酶联免疫吸附测定(DAS-ELISA)比较,在从田间、温室和离体培养植物采集的叶片上测试了该方法的可靠性。观察到这两种方法之间具有高度相关性。还通过检测从秘鲁利马国际马铃薯中心获得的感染样品对mRT-PCR进行了评估;该检测证实了其高可靠性和灵敏度。