Carpentier David C J, Van Loggerenberg Alexander, Dieckmann Nele M G, Smith Geoffrey L
Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK.
Present address: Cambridge Institute for Medical Research (CIMR), University of Cambridge, Cambridge Biomedical Campus, CB2 0XY, UK.
J Gen Virol. 2017 Jun;98(6):1500-1514. doi: 10.1099/jgv.0.000816. Epub 2017 Jun 20.
Egress of vaccinia virus from its host cell is mediated by the microtubule-associated motor kinesin-1, and three viral proteins, A36 and the F12/E2 complex, have been implicated in this process. Deletion of F12 expression causes a more severe reduction in egress than deletion of A36 but whether these proteins are involved in the same or different mechanisms of kinesin-1 recruitment is unknown. Here it is shown that a virus lacking both proteins forms a smaller plaque than mutants lacking either gene alone, indicating non-redundant functions. A36 not only links virions directly to kinesin-1 but also nucleates actin polymerization to propel surface virions away from the host cell. To address the relative importance of these functions for virus spread, a panel of recombinant viruses was constructed in which the ability of A36 to bind kinesin-1 or to nucleate actin polymerization was abrogated individually or together, in the presence or absence of F12 expression. Analysis of these viruses revealed that in the presence of the F12 protein, loss of kinesin-1 interaction made a greater contribution to plaque size than did the formation of actin tails. However in the absence of F12, the ability of A36 to promote egress was abrogated. Therefore, the ability of A36 to promote egress by kinesin-1 is reliant on the F12 protein.
痘苗病毒从宿主细胞的释放由微管相关马达蛋白驱动蛋白-1介导,三种病毒蛋白,即A36和F12/E2复合物,参与了这一过程。缺失F12表达导致的释放减少比缺失A36更为严重,但这些蛋白是否参与驱动蛋白-1募集的相同或不同机制尚不清楚。本文表明,一种同时缺失这两种蛋白的病毒形成的蚀斑比单独缺失任一基因的突变体更小,表明它们具有非冗余功能。A36不仅将病毒粒子直接与驱动蛋白-1相连,还能促进肌动蛋白聚合,以推动表面的病毒粒子远离宿主细胞。为了探讨这些功能对病毒传播的相对重要性,构建了一组重组病毒,在有或无F12表达的情况下,分别或同时消除A36与驱动蛋白-1结合或促进肌动蛋白聚合的能力。对这些病毒的分析表明,在存在F12蛋白的情况下,驱动蛋白-1相互作用的丧失对蚀斑大小的影响比肌动蛋白尾的形成更大。然而,在没有F12的情况下,A36促进释放的能力被消除。因此,A36通过驱动蛋白-1促进释放的能力依赖于F12蛋白。