Blanchard Emmanuelle, Roingeard Philippe
INSERM U966, Université François Rabelais and CHRU de Tours, Tours, Cedex 37032, France.
Cell Microbiol. 2015 Jan;17(1):45-50. doi: 10.1111/cmi.12372. Epub 2014 Oct 31.
Many viruses that replicate in the cytoplasm compartmentalize their genome replication and transcription in specific subcellular microenvironments or organelle-like structures, to increase replication efficiency and protect against host cell defences. Recent studies have investigated the complex membrane rearrangements induced by diverse positive-strand RNA viruses, which are of two morphotypes : membrane invagination towards the lumen of the endoplasmic reticulum (ER) or other specifically targeted organelles and double-membrane vesicles (DMVs) formed by extrusion of the ER membrane. DMVs resemble small autophagosomes and the viruses inducing these intriguing organelles are known to promote autophagy, suggesting a potential link between DMVs and the autophagic pathway. In this review, we summarize recent findings concerning the biogenesis, architecture and role of DMVs in the life cycle of viruses from different families and discuss their possible connection to autophagy or other related pathways.
许多在细胞质中复制的病毒会将其基因组复制和转录分隔在特定的亚细胞微环境或类似细胞器的结构中,以提高复制效率并抵御宿主细胞的防御机制。最近的研究调查了由多种正链RNA病毒诱导的复杂膜重排,这些病毒有两种形态类型:向内质网(ER)或其他特定靶向细胞器的腔内的膜内陷,以及由ER膜挤出形成的双膜囊泡(DMV)。DMV类似于小型自噬体,已知诱导这些有趣细胞器的病毒会促进自噬,这表明DMV与自噬途径之间存在潜在联系。在这篇综述中,我们总结了关于DMV在不同病毒家族生命周期中的生物发生、结构和作用的最新发现,并讨论了它们与自噬或其他相关途径的可能联系。