Boyce Thompson Institute at Cornell University, Tower Road, Ithaca, NY 14853, USA.
Department of Entomology, Cornell University, Ithaca, NY 14853, USA.
Virology. 2019 Jan 15;527:1-11. doi: 10.1016/j.virol.2018.10.022. Epub 2018 Nov 13.
The baculovirus Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is a model enveloped DNA virus that infects and replicates in lepidopteran insect cells, and can efficiently enter a wide variety of non-host cells. Budded virions of AcMNPV enter cells by endocytosis and traffic to the nucleus where the virus initiates gene expression and genome replication. While trafficking of nucleocapsids by actin propulsion has been studied in detail, other important components of trafficking during entry remain poorly understood. We used a recombinant AcMNPV virus expressing an EGFP reporter in combination with an RNAi screen in Drosophila DL1 cells, to identify host proteins involved in AcMNPV entry. The RNAi screen targeted 86 genes involved in vesicular trafficking, including genes coding for VPS and ESCRT proteins, Rab GTPases, Exocyst proteins, and Clathrin adaptor proteins. We identified 24 genes required for efficient virus entry and reporter expression, and 4 genes that appear to restrict virus entry.
杆状病毒 Autographa californica 多角体病毒(AcMNPV)是一种模式包膜 DNA 病毒,可感染和复制鳞翅目昆虫细胞,并能有效地进入各种非宿主细胞。AcMNPV 的芽生病毒通过内吞作用进入细胞,并运输到细胞核,在那里病毒开始基因表达和基因组复制。虽然核衣壳通过肌动蛋白推进的运输已被详细研究,但进入过程中其他重要的运输成分仍知之甚少。我们使用表达 EGFP 报告基因的重组 AcMNPV 病毒与 Drosophila DL1 细胞中的 RNAi 筛选相结合,鉴定参与 AcMNPV 进入的宿主蛋白。RNAi 筛选针对参与囊泡运输的 86 个基因,包括编码 VPS 和 ESCRT 蛋白、Rab GTPases、外泌体蛋白和网格蛋白衔接蛋白的基因。我们鉴定了 24 个对病毒进入和报告基因表达有效所需的基因,以及 4 个似乎限制病毒进入的基因。