Liu Xiao-Dong, Zhang Zeng-Yan, Liu Yan, Xin Zhi-Yong
Key Laboratory of Crop Genetics and Breeding, Ministry of Agriculture, Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
Yi Chuan Xue Bao. 2005 Sep;32(9):942-7.
A wheat-Thinopyrum intermedium translocation line YW642 possesses the resistance to GAV serotype of barley yellow dwarf virus (BYDV), in which the resistance gene Bdv2 is derived from the chromosome 7X of Thinopyrum intermedium group 7. It is interesting to analyze BYDV accumulation content in the resistant and susceptible wheat plants for controlling BYDV disease and understanding the resistance mechanism against BYDV. In the paper, semi-quantitative reverse-transcription PCR (RT-PCR) was used to detect and quantify BYDV-GAV in the resistant and susceptible plants using specific primers for the coat protein (CP) and RNA-dependent RNA polymerase (RdRp) genes of BYDV-GAV serotype. On the inoculation site, the amount of the virus in the resistant wheat line (YW642) was much lower compared to the susceptible sib line (YW641). There was small amount of the virus could be detected in YW642 at 2-5 days post infestation (dpi), afterwards the amount of virus decreased and no virus could be detected at 14 and 16 dpi. In the uninoculated upper leaves, no BYDV was detected in YW642 from 1 to 14 dpi, while the virus could be detected at 3 dpi and then accumulated rapidly in YW641. These results showed at molecular level that the replication and/or movement of BYDV-GAV were strongly suppressed in YW642, presumably owing to the action of the BdV2 gene.
小麦-中间偃麦草易位系YW642对大麦黄矮病毒(BYDV)的GAV血清型具有抗性,其中抗性基因Bdv2源自中间偃麦草第7组染色体7X。分析抗性和感病小麦植株中BYDV的积累含量,对于控制BYDV病害和了解抗BYDV机制具有重要意义。本文利用半定量逆转录PCR(RT-PCR)技术,使用针对BYDV-GAV血清型外壳蛋白(CP)和RNA依赖RNA聚合酶(RdRp)基因的特异性引物,检测并定量抗性和感病植株中的BYDV-GAV。在接种部位,抗性小麦品系(YW642)中的病毒量比感病姊妹系(YW641)低得多。在侵染后2-5天(dpi),YW642中可检测到少量病毒,之后病毒量下降,在14和16 dpi时未检测到病毒。在未接种的上部叶片中,YW642在1至14 dpi未检测到BYDV,而YW641在3 dpi可检测到病毒,然后迅速积累。这些结果在分子水平上表明,BYDV-GAV在YW642中的复制和/或移动受到强烈抑制,推测是由于BdV2基因的作用。