Institute for Infection and Immunity, St. George's University of London, London, United Kingdom.
PLoS One. 2020 Mar 5;15(3):e0229877. doi: 10.1371/journal.pone.0229877. eCollection 2020.
Rhabdoviruses are enveloped negative-sense RNA viruses that have numerous biotechnological applications. However, recovering plant rhabdoviruses from cDNA remains difficult due to technical difficulties such as the need for concurrent in planta expression of the viral genome together with the viral nucleoprotein (N), phosphoprotein (P) and RNA-dependent RNA polymerase (L) and viral genome instability in E. coli. Here, we developed a negative-sense minigenome cassette for Lettuce necrotic yellows virus (LNYV). We introduced introns into the unstable viral ORF and employed Agrobacterium tumefaciens to co-infiltrate Nicotiana with the genes for the N, P, and L proteins together with the minigenome cassette. The minigenome cassette included the Discosoma sp. red fluorescent protein gene (DsRed) cloned in the negative-sense between the viral trailer and leader sequences which were placed between hammerhead and hepatitis delta ribozymes. In planta DsRed expression was demonstrated by western blotting while the appropriate splicing of introduced introns was confirmed by sequencing of RT-PCR product.
弹状病毒是带包膜的负义 RNA 病毒,具有许多生物技术应用。然而,由于技术上的困难,如需要在植物体内同时表达病毒基因组和病毒核蛋白(N)、磷蛋白(P)和 RNA 依赖性 RNA 聚合酶(L),以及大肠杆菌中病毒基因组的不稳定性,从 cDNA 中回收植物弹状病毒仍然很困难。在这里,我们为莴苣坏死性黄化病毒(LNYV)开发了一个负义小基因盒。我们将不稳定的病毒 ORF 中的内含子引入,并利用根癌农杆菌共浸润烟草,将 N、P 和 L 蛋白的基因与小基因盒一起导入。小基因盒包括克隆在病毒尾部和前导序列之间的负义链上的 Discosoma sp. 红色荧光蛋白基因(DsRed),这些序列位于锤头和丙型肝炎德尔塔核酶之间。通过 Western blot 证明了体内 DsRed 的表达,通过 RT-PCR 产物测序确认了引入内含子的适当剪接。