Stare Katja, Coll Anna, Gutiérrez-Aguirre Ion, Žnidarič Magda Tušek, Ravnikar Maja, Kežar Andreja, Kavčič Luka, Podobnik Marjetka, Gruden Kristina
Department of Biotechnology and Systems Biology, National Institute of Biology, Ljubljana, Slovenia.
University of Nova Gorica, Nova Gorica, Slovenia.
Bio Protoc. 2020 Jul 20;10(14):e3692. doi: 10.21769/BioProtoc.3692.
Potato virus Y (PVY), the type member of the genus (family ), is the most widespread virus affecting potato and is included in the top five most economically detrimental plant viruses. Recently, the structure of the PVY virion has been determined by cryo-electron microscopy, which has opened the doors to functional studies that explore the involvement of selected amino acids in different stages of the viral cycle. The only way to functionally challenge the role of particular amino acids in the coat protein of PVY, or in other viral proteins, is by using cDNA clones. The use and manipulation of PVY cDNA clones, unlike those of other potyviruses, has been traditionally impaired by the toxicity that certain sequences within the PVY genome pose to . Here, we describe the use of a published PVY cDNA clone, which harbours introns that overcome the aforementioned toxicity, to explore the effects of different coat protein modifications on viral infection. The protocol includes manipulation of the cDNA clone in , biolistic inoculation of plants with the constructed clones, observation of the biological effects on plants, quantification of cDNA clones by reverse transcription quantitative PCR, and confirmation of virion formation by transmission electron microscopy. Future possibilities involve the use of PVY cDNA clones tagged with fluorescent protein reporters to allow further insights into the effects of coat protein mutations on the cell-to-cell movement of PVY virions.
马铃薯Y病毒(PVY)是马铃薯Y病毒属(马铃薯Y病毒科)的典型成员,是影响马铃薯的分布最为广泛的病毒,位列对经济危害最大的五大植物病毒之中。最近,通过冷冻电子显微镜已确定了PVY病毒粒子的结构,这为开展功能研究打开了大门,此类研究旨在探究特定氨基酸在病毒周期不同阶段所起的作用。在功能上对PVY外壳蛋白或其他病毒蛋白中特定氨基酸的作用提出质疑的唯一方法是使用cDNA克隆。与其他马铃薯Y病毒属病毒的cDNA克隆不同,PVY cDNA克隆的使用和操作传统上受到PVY基因组内某些序列对大肠杆菌产生的毒性的影响。在此,我们描述了如何使用已发表的PVY cDNA克隆(其含有可克服上述毒性的内含子)来探究不同外壳蛋白修饰对病毒感染的影响。该方案包括在大肠杆菌中对cDNA克隆进行操作、用构建好的克隆对植物进行生物弹道接种、观察对植物的生物学效应、通过逆转录定量PCR对cDNA克隆进行定量以及通过透射电子显微镜确认病毒粒子的形成。未来的可能性包括使用带有荧光蛋白报告基因标记的PVY cDNA克隆,以便进一步深入了解外壳蛋白突变对PVY病毒粒子细胞间移动的影响。