Gosselin-Grenet Anne-Sophie, Mottet-Osman Geneviève, Roux Laurent
Department of Microbiology and Molecular Medicine, University of Geneva Medical School, CMU, 1 rue Michel-Servet, CH-1211 Geneva 4, Switzerland.
Virology. 2006 Jan 20;344(2):296-303. doi: 10.1016/j.virol.2005.09.035. Epub 2005 Oct 17.
Detergent resistant membranes (DRMs) are the site of assembly for a variety of viruses. Here, we make use of Sendai virus mutant proteins that are not packaged into virus particles to determine the involvement of this assembly for the virus particle production. We found that, in the context of an infection, (1) all the Sendai virus proteins associated in part with DRMs, (2) mutant HN and M proteins not packaged into virus particles were similarly part of this association, (3) after M protein suppression resulting in a significant reduction of virus production, the floatation profile of the other viral proteins was not altered and finally (4) cellular cholesterol depletion did not decrease the virus particle production, although it somehow reduced their virus infectivity. These results led us to conclude that the assembly complex found in DRM fractions does not constitute a direct precursor of virus particle budding.
耐去污剂膜(DRM)是多种病毒的组装位点。在此,我们利用未包装进病毒颗粒的仙台病毒突变蛋白来确定这种组装与病毒颗粒产生之间的关联。我们发现,在感染的情况下,(1)所有仙台病毒蛋白部分与DRM相关联,(2)未包装进病毒颗粒的突变HN和M蛋白同样是这种关联的一部分,(3)在M蛋白受到抑制导致病毒产生显著减少后,其他病毒蛋白的漂浮分布未改变,最后(4)细胞胆固醇耗竭并未降低病毒颗粒的产生,尽管这在某种程度上降低了它们的病毒感染性。这些结果使我们得出结论,在DRM组分中发现的组装复合体并不构成病毒颗粒出芽的直接前体。