Proceedings of the National Academy of Sciences · 2006 · 130 citations · 41 references
Life SciencesCell BiologyMolecular BiologyMembrane BiophysicsMolecular VirologyVirologyMembrane FusionViral EntryViral InfectionsViral StructureVirus EntryVirus StructureEntry Of Enveloped VirusesOuter Membrane StructurePoxvirus BiologyViral Envelope GlycoproteinsViral Envelope ProteinsViral Envelope StructureViral Membrane FusionVirus-host Membrane Interactions
Hitherto, all enveloped viruses were thought to shed their lipid membrane during entry into cells by membrane fusion. The extracellular form of Vaccinia virus has two lipid envelopes surrounding the virus core, and consequently a single fusion event will not deliver a naked core into the cell. Here we report a previously underscribed mechanism in which the outer viral membrane is disrupted by a ligand-induced nonfusogenic reaction, followed by the fusion of the inner viral membrane with the plasma membrane and penetration of the virus core into the cytoplasm. The dissolution of the outer envelope depends on interactions with cellular polyanionic molecules and requires the virus glycoproteins A34 and B5. This discovery represents a remarkable example of how viruses manipulate biological membranes, solves the topological problem of how a double-enveloped virus enters cells, reveals a new effect of polyanions on viruses, and provides a therapeutic approach for treatment of poxvirus infections, such as smallpox.
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Actin-based motility of vaccinia virus
Sally Cudmore, Pascale Cossart, Gareth Griffiths et al. · Nature · 1995 · 429 citations