Condezo Gabriela N, San Martín Carmen
Department of Macromolecular Structures, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
PLoS Pathog. 2017 Apr 27;13(4):e1006320. doi: 10.1371/journal.ppat.1006320. eCollection 2017 Apr.
Adenovirus (AdV) morphogenesis is a complex process, many aspects of which remain unclear. In particular, it is not settled where in the nucleus assembly and packaging occur, and whether these processes occur in a sequential or a concerted manner. Here we use immunofluorescence and immunoelectron microscopy (immunoEM) to trace packaging factors and structural proteins at late times post infection by either wildtype virus or a delayed packaging mutant. We show that representatives of all assembly factors are present in the previously recognized peripheral replicative zone, which therefore is the AdV assembly factory. Assembly intermediates and abortive products observed in this region favor a concurrent assembly and packaging model comprising two pathways, one for capsid proteins and another one for core components. Only when both pathways are coupled by correct interaction between packaging proteins and the genome is the viral particle produced. Decoupling generates accumulation of empty capsids and unpackaged cores.
腺病毒(AdV)的形态发生是一个复杂的过程,其中许多方面仍不清楚。特别是,病毒在细胞核内的组装和包装位置以及这些过程是以顺序方式还是协同方式发生尚无定论。在这里,我们使用免疫荧光和免疫电子显微镜(immunoEM)来追踪野生型病毒或延迟包装突变体感染后晚期的包装因子和结构蛋白。我们发现,所有组装因子的代表都存在于先前识别的外周复制区,因此该区域是AdV组装工厂。在该区域观察到的组装中间体和流产产物支持一种同时进行组装和包装的模型,该模型包括两条途径,一条用于衣壳蛋白,另一条用于核心成分。只有当两条途径通过包装蛋白与基因组之间的正确相互作用耦合时,才能产生病毒颗粒。解耦会导致空衣壳和未包装核心的积累。