Institute for Molecular Virology, University of Wisconsin-Madison, Madison, Wisconsin 53706, USA.
Annu Rev Microbiol. 2010;64:241-56. doi: 10.1146/annurev.micro.112408.134012.
Positive-strand RNA virus genome replication is invariably associated with extensively rearranged intracellular membranes. Recent biochemical and electron microscopy analyses, including three-dimensional electron microscope tomographic imaging, have fundamentally advanced our understanding of the ultrastructure and function of organelle-like RNA replication factories. Notably, for a range of positive-strand RNA viruses embodying many major differences, independent studies have revealed multiple common principles. These principles include that RNA replication often occurs inside numerous virus-induced vesicles invaginated or otherwise elaborated from a continuous, often endoplasmic reticulum-derived membrane network. Where analyzed, each such vesicle typically contains only one or a few genome replication intermediates in conjunction with many copies of viral nonstructural proteins. In addition, these genome replication compartments often are closely associated with sites of virion assembly and budding. Our understanding of these complexes is growing, providing substantial new insights into the organization, coordination, and potential control of crucial processes in virus replication.
正链 RNA 病毒基因组的复制总是与广泛重排的细胞内膜有关。最近的生化和电子显微镜分析,包括三维电子显微镜断层成像,从根本上提高了我们对类细胞器 RNA 复制工厂的超微结构和功能的理解。值得注意的是,对于一系列具有许多主要差异的正链 RNA 病毒,独立的研究揭示了多个共同的原则。这些原则包括:RNA 复制通常发生在大量病毒诱导的小泡内,这些小泡是从连续的、通常来源于内质网的膜网络内陷或其他方式形成的。在已分析的情况下,每个这样的小泡通常仅包含一个或几个基因组复制中间体,以及许多病毒非结构蛋白的拷贝。此外,这些基因组复制隔室通常与病毒粒子组装和出芽的部位密切相关。我们对这些复合物的理解正在不断发展,为病毒复制过程中的组织、协调和潜在控制提供了重要的新见解。