Gal-On A, Meiri E, Huet H, Hua W J, Raccah B, Gaba V
Department of Virology, Agricultural Research Organization, Volcani Center, Bet Dagan, Israel.
J Gen Virol. 1995 Dec;76 ( Pt 12):3223-7. doi: 10.1099/0022-1317-76-12-3223.
An infectious full-length cDNA clone of the RNA genome of the potyvirus zucchini yellow mosaic virus (ZYMV) was constructed under the control of the cauliflower mosaic virus 35S promoter. All squash, cucumber, melon and watermelon plants inoculated with the cloned cDNA of ZYMV by particle bombardment become infected. Bombardment technology is 10(6)-fold more effective than mechanical inoculation. Due to the great increase in efficiency, ineffective constructs now became infective (i.e. cDNA under the control of the 35S promoter without the NOS terminator; with an addition of 127 nucleotides at the 5' end of the viral cDNA; uncapped transcripts), and the infectivity of capped-transcripts was maximized. Inoculation by particle bombardment produced visual symptoms rapidly (3-4 days), allowing the detection of viral coat protein and virions after 2 and 3 days in systemically infected leaves and inoculated cotyledons respectively.
在花椰菜花叶病毒35S启动子的控制下,构建了马铃薯Y病毒西葫芦黄花叶病毒(ZYMV)RNA基因组的感染性全长cDNA克隆。通过粒子轰击接种ZYMV克隆cDNA的所有南瓜、黄瓜、甜瓜和西瓜植株均被感染。轰击技术的效率比机械接种高10^6倍。由于效率大幅提高,无效构建体现在变得具有感染性(即35S启动子控制下无NOS终止子的cDNA;病毒cDNA 5'端添加127个核苷酸;未加帽的转录本),加帽转录本的感染性也达到了最大化。通过粒子轰击接种能迅速产生可见症状(3 - 4天),分别在系统感染叶片和接种子叶中,2天和3天后就能检测到病毒外壳蛋白和病毒粒子。