Meyer M, Dessens J T
Station de Pathologie Végétale, Institut National de la Recherche Agronomique, Versailles, France.
J Gen Virol. 1997 Dec;78 ( Pt 12):3147-51. doi: 10.1099/0022-1317-78-12-3147.
Full-length cDNAs of barley mild mosaic bymovirus RNA1 and RNA2 were cloned downstream of a modified cauliflower mosaic virus 35S promoter with double enhancer. Mechanical inoculation of barley seedlings with a mixture of both cDNAs resulted in systemic mosaic symptoms, typical of barley mild mosaic virus infection. The presence of both RNA species and their gene products in the systemically infected leaves was demonstrated by RT-PCR and Western blot analyses, respectively. Virions were detected by immunogold labelling, demonstrating that the RNAs are encapsidated. This is the first report of the 35S promoter used in successfully infecting a monocot plant host with cDNA from a strictly monocot plant RNA virus.
大麦轻花叶病毒RNA1和RNA2的全长cDNA被克隆到带有双增强子的修饰花椰菜花叶病毒35S启动子下游。用两种cDNA的混合物对大麦幼苗进行机械接种,导致出现系统性花叶症状,这是大麦轻花叶病毒感染的典型症状。通过RT-PCR和蛋白质免疫印迹分析分别证实了系统感染叶片中两种RNA种类及其基因产物的存在。通过免疫金标记检测到病毒粒子,表明RNA被衣壳化。这是首次报道使用35S启动子成功地用来自严格单子叶植物RNA病毒的cDNA感染单子叶植物宿主。