Le Blanc Isabelle, Luyet Pierre-Philippe, Pons Véronique, Ferguson Charles, Emans Neil, Petiot Anne, Mayran Nathalie, Demaurex Nicolas, Fauré Julien, Sadoul Rémy, Parton Robert G, Gruenberg J
Biochemistry Department, University of Geneva, 30 quai E. Ansermet, 1211 Geneva 4, Switzerland.
Nat Cell Biol. 2005 Jul;7(7):653-64. doi: 10.1038/ncb1269. Epub 2005 Jun 12.
During viral infection, fusion of the viral envelope with endosomal membranes and nucleocapsid release were thought to be concomitant events. We show here that for the vesicular stomatitis virus they occur sequentially, at two successive steps of the endocytic pathway. Fusion already occurs in transport intermediates between early and late endosomes, presumably releasing the nucleocapsid within the lumen of intra-endosomal vesicles, where it remains hidden. Transport to late endosomes is then required for the nucleocapsid to be delivered to the cytoplasm. This last step, which initiates infection, depends on the late endosomal lipid lysobisphosphatidic acid (LBPA) and its putative effector Alix/AIP1, and is regulated by phosphatidylinositol-3-phosphate (PtdIns3P) signalling via the PtdIns3P-binding protein Snx16. We conclude that the nucleocapsid is exported into the cytoplasm after the back-fusion of internal vesicles with the limiting membrane of late endosomes, and that this process is controlled by the phospholipids LBPA and PtdIns3P and their effectors.
在病毒感染过程中,病毒包膜与内体膜的融合以及核衣壳的释放被认为是同时发生的事件。我们在此表明,对于水疱性口炎病毒而言,它们是在胞吞途径的两个连续步骤中依次发生的。融合已经在早期和晚期内体之间的运输中间体中发生,大概是将核衣壳释放到内体泡腔内,在那里它一直处于隐藏状态。然后需要将其运输到晚期内体,以便将核衣壳递送至细胞质。启动感染的这最后一步取决于晚期内体脂质赖氨酰二磷脂酸(LBPA)及其假定的效应物Alix/AIP1,并通过磷脂酰肌醇-3-磷酸(PtdIns3P)结合蛋白Snx16受磷脂酰肌醇-3-磷酸(PtdIns3P)信号传导的调节。我们得出结论,核衣壳是在内部泡囊与晚期内体的限制膜反向融合后被输出到细胞质中的,并且这一过程受磷脂LBPA和PtdIns3P及其效应物的控制。