Microbiology Graduate Group, University of California, Berkeley, Berkeley, CA 94720.
Department of Molecular & Cell Biology, University of California, Berkeley, Berkeley, CA 94720.
Mol Biol Cell. 2021 Aug 1;32(16):1433-1445. doi: 10.1091/mbc.E20-11-0705. Epub 2021 Jun 16.
The baculovirus multiple nucleopolyhedrovirus (AcMNPV), a pathogen of lepidopteran insects, has a striking dependence on the host cell actin cytoskeleton. During the delayed-early stage of infection, AcMNPV was shown to induce the accumulation of actin at the cortex of infected cells. However, the dynamics and molecular mechanism of cortical actin assembly remained unknown. Here, we show that AcMNPV induces dynamic cortical clusters of dot-like actin structures that mediate degradation of the underlying extracellular matrix and therefore function similarly to clusters of invadosomes in mammalian cells. Furthermore, we find that the AcMNPV protein actin-rearrangement-inducing factor-1 (ARIF-1), which was previously shown to be necessary and sufficient for cortical actin assembly and efficient viral infection in insect hosts, is both necessary and sufficient for invadosome formation. We mapped the sequences within the C-terminal cytoplasmic region of ARIF-1 that are required for invadosome formation and identified individual tyrosine and proline residues that are required for organizing these structures. Additionally, we found that ARIF-1 and the invadosome-associated proteins cortactin and the Arp2/3 complex localize to invadosomes and Arp2/3 complex is required for their formation. These ARIF-1-induced invadosomes may be important for the function of ARIF-1 in systemic virus spread.
杆状病毒多角体病毒(AcMNPV)是鳞翅目昆虫的病原体,对宿主细胞肌动蛋白细胞骨架有明显的依赖性。在感染的晚期早期,AcMNPV 被显示诱导肌动蛋白在感染细胞的皮质处积累。然而,皮质肌动蛋白组装的动力学和分子机制仍然未知。在这里,我们表明 AcMNPV 诱导动态皮质点状肌动蛋白结构簇,介导细胞外基质的降解,因此类似于哺乳动物细胞中入侵小体的簇。此外,我们发现 AcMNPV 蛋白肌动蛋白重排诱导因子-1(ARIF-1),以前被证明对皮质肌动蛋白组装和昆虫宿主中有效的病毒感染是必要和充分的,对于入侵小体的形成是必要和充分的。我们绘制了 ARIF-1 中 C 端细胞质区域内的序列,这些序列对于入侵小体的形成是必需的,并确定了组织这些结构所需的单个酪氨酸和脯氨酸残基。此外,我们发现 ARIF-1 和入侵小体相关蛋白 cortactin 和 Arp2/3 复合物定位于入侵小体,并且 Arp2/3 复合物是其形成所必需的。这些 ARIF-1 诱导的入侵小体可能对 ARIF-1 在全身病毒传播中的功能很重要。