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Ligand-induced and nonfusogenic dissolution of a viral membrane

机译:配体诱导的和非融合的病毒膜溶解

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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.
机译:迄今为止,人们认为所有包膜病毒在通过膜融合进入细胞的过程中都会脱落其脂膜。痘苗病毒的细胞外形式在病毒核心周围有两个脂质包膜,因此,一次融合事件不会将裸露的核心传递到细胞中。在这里,我们报道了一个先前描述的机制,其中外病毒膜被配体诱导的非融合反应破坏,然后内病毒膜与质膜融合,病毒核心渗透到细胞质中。外壳的溶解取决于与细胞聚阴离子分子的相互作用,并需要病毒糖蛋白A34和B5。这一发现代表了病毒如何操纵生物膜,解决双重包裹病毒如何进入细胞的拓扑问题,揭示了聚阴离子对病毒的新作用以及为痘病毒感染(如天花)提供治疗方法的杰出例子。 。

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