Malmstrom Carolyn M, Shu Ruijie
Department of Plant Biology, 166 Plant Biology Laboratories, Michigan State University, East Lansing, MI 48824, USA.
J Virol Methods. 2004 Sep 1;120(1):69-78. doi: 10.1016/j.jviromet.2004.04.005.
Two novel multiplexed RT-PCR assays that can efficiently detect and distinguish among different barley and cereal yellow dwarf viruses (B/CYDVs) are described. The basic multiplex can produce two fragments simultaneously, a approximately 830-bp fragment indicating the presence of the BYDV-PAV, BYDV-MAV, or BYDV-SGV viruses and a approximately 372-bp fragment indicating the presence of the CYDV-RPV, BYDV-RMV, or BYDV-GPV viruses. The enhanced multiplex produces two additional fragments, which further differentiate between BYDV-PAV, BYDV-MAV, and BYDV-SGV. These assays fulfill the critical need for a streamlined diagnostic procedure for B/CYDVs that can be cost-effectively applied to large numbers of small samples. The assays are useful not only in the basic diagnosis of B/CYDVs, but also for studies examining the ecological roles of B/CYDVs in natural systems and for longer-term epidemiological studies of grasses and cereals.
本文描述了两种新型多重逆转录聚合酶链反应(RT-PCR)检测方法,它们能够高效检测并区分不同的大麦和谷类黄矮病毒(B/CYDVs)。基本多重检测法可同时产生两个片段,一个约830bp的片段表明存在大麦黄矮病毒-PAV(BYDV-PAV)、大麦黄矮病毒-MAV(BYDV-MAV)或大麦黄矮病毒-SGV(BYDV-SGV),另一个约372bp的片段表明存在谷类黄矮病毒-RPV(CYDV-RPV)、大麦黄矮病毒-RMV(BYDV-RMV)或大麦黄矮病毒-GPV(BYDV-GPV)。增强多重检测法还会产生另外两个片段,可进一步区分BYDV-PAV、BYDV-MAV和BYDV-SGV。这些检测方法满足了对B/CYDVs简化诊断程序的迫切需求,该程序可经济高效地应用于大量小样本。这些检测方法不仅对B/CYDVs的基本诊断有用,还可用于研究B/CYDVs在自然系统中的生态作用以及对禾本科植物和谷类作物进行长期的流行病学研究。