Key result
Recent advances in cell biology and 3D cellular imaging reveal how specific viral proteins interact with cellular processes to form membrane vesicles during positive-strand RNA virus replication.
This review highlights how advances in 3D cellular imaging elucidate the formation of membrane vesicles during positive-strand RNA virus replication.
Elucidates viral replication mechanisms; leaves open targeted antiviral development pending functional and clinical validation.
Infection of cells by positive-strand RNA viruses generates large numbers of membrane vesicles that provide sites for genome replication. Vesicle formation is initiated by targeting replicase proteins to the cytosolic face of membrane-bound organelles where protein assembly induces membrane curvature. This can result in invagination into the limiting membrane of membrane compartments or induce vesicle budding into the cytoplasm. The new membranes are thought to provide a platform to concentrate proteins, lipids and nucleotides that are required for genome replication. This article describes how recent advances in cell biology and cellular imaging can reveal these structures in 3D, and begin to define how they are formed in terms of effects of specific viral proteins on specific cellular processes.
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Cottam et al. (2009) conducted a review in Positive-strand RNA virus infection. Recent advances in cell biology and 3D cellular imaging reveal how specific viral proteins interact with cellular processes to form membrane vesicles during positive-strand RNA virus replication.
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