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Development of three full-length infectious cDNA clones of distinct brassica yellows virus genotypes for agrobacterium-mediated inoculation

机译:农杆菌介导的三种不同芸苔属黄病毒基因型全长感染性cDNA克隆的建立

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Brassica yellows virus is a newly identified species in the genus of Polerovirus within the family Luteoviridae. Brassica yellows virus (BrYV) is prevalently distributed throughout Mainland China and South Korea, is an important virus infecting cruciferous crops. Based on six BrYV genomic sequences of isolates from oilseed rape, rutabaga, radish, and cabbage, three genotypes, BrYV-A, BrYV-B, and BrYV-C, exist, which mainly differ in the 5' terminal half of the genome. BrYV is an aphid-transmitted and phloem-limited virus. The use of infectious cDNA clones is an alternative means of infecting plants that allows reverse genetic studies to be performed. In this study, full-length cDNA clones of BrYV-A, recombinant BrYV5B3A, and BrYV-C were constructed under control of the cauliflower mosaic virus 35S promoter. An agrobacterium-mediated inoculation system of Nicotiana benthamiana was developed using these cDNA clones. Three days after infiltration with full-length BrYV cDNA clones, necrotic symptoms were observed in the inoculated leaves of N. benthamiana; however, no obvious symptoms appeared in the upper leaves. Reverse transcription-PCR (RT-PCR) and western blot detection of samples from the upper leaves showed that the maximum infection efficiency of BrYVs could reach 100%. The infectivity of the BrYV-A, BrYV-5B3A, and BrYV-C cDNA clones was further confirmed by northern hybridization. The system developed here will be useful for further studies of BrYV, such as host range, pathogenicity, viral gene functions, and plant-virus-vector interactions, and especially for discerning the differences among the three genotypes. (C) 2014 Elsevier B.V. All rights reserved.
机译:芸苔黄病毒是黄体病毒科中新发现的一种杆状病毒属。芸苔黄病毒(BrYV)广泛分布于中国大陆和韩国,是一种重要的病毒,可感染十字花科作物。基于来自油菜,大头菜,萝卜和甘蓝的分离物的六个BrYV基因组序列,存在三种基因型BrYV-A,BrYV-B和BrYV-C,其主要区别在于基因组的5'末端一半。 BrYV是一种蚜虫传播的韧皮部限制病毒。感染性cDNA克隆的使用是感染植物的另一种方法,可以进行反向遗传研究。在这项研究中,在花椰菜花叶病毒35S启动子的控制下构建了BrYV-A,重组BrYV5B3A和BrYV-C的全长cDNA克隆。利用这些cDNA克隆开发了农杆菌介导的本氏烟草接种系统。全长BrYV cDNA克隆渗入后三天,在本氏烟草的接种叶子中观察到坏死症状。但是,上部叶片没有明显的症状。逆转录-聚合酶链反应(RT-PCR)和蛋白质印迹检测的上部叶样品表明,BrYVs的最大感染效率可以达到100%。通过Northern杂交进一步证实了BrYV-A,BrYV-5B3A和BrYV-C cDNA克隆的感染性。这里开发的系统将对进一步研究BrYV有用,例如宿主范围,致病性,病毒基因功能和植物-病毒-载体相互作用,尤其是辨别这三种基因型之间的差异。 (C)2014 Elsevier B.V.保留所有权利。

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