Sodeik B, Cudmore S, Ericsson M, Esteban M, Niles E G, Griffiths G
Cell Biology Program, European Molecular Biology Laboratory, Heidelberg, Germany.
J Virol. 1995 Jun;69(6):3560-74. doi: 10.1128/JVI.69.6.3560-3574.1995.
The cytoplasmic assembly of vaccinia virus begins with the transformation of a two-membraned cisterna derived from the intermediate compartment between the endoplasmic reticulum and the Golgi complex. This cisterna develops into a viral crescent which eventually forms a spherical immature virus (IV) that matures into the intracellular mature virus (IMV). Using immunoelectron microscopy, we determined the subcellular localization of p32 and p14, two membrane-associated proteins of vaccinia virus. p32 was associated with vaccinia virus membranes at all stages of virion assembly, starting with the viral crescents, as well as with the membranes which accumulated during the inhibition of assembly by rifampin. There was also low but significant labelling of membranes of some cellular compartments, especially those in the vicinity of the Golgi complex. In contrast, anti-p14 labelled neither the crescents nor the IV but gave strong labelling of an intermediate form between IV and IMV and was then associated with all later viral forms. This protein was also not significantly detected on identifiable cellular membranes. Both p32 and p14 were abundantly expressed on the surface of intact IMV. Our data are consistent with a model whereby p32 would become inserted into cellular membranes before being incorporated into the crescents whereas p14 would be posttranslationally associated with the viral outer membrane at a specific later stage of the viral life cycle.
痘苗病毒的胞质装配始于源自内质网和高尔基体复合体之间中间区室的双膜池的转变。这个池发展成病毒新月体,最终形成球形未成熟病毒(IV),其成熟为细胞内成熟病毒(IMV)。利用免疫电子显微镜,我们确定了痘苗病毒的两种膜相关蛋白p32和p14的亚细胞定位。从病毒新月体开始,p32在病毒体装配的所有阶段都与痘苗病毒膜相关,以及与利福平抑制装配过程中积累的膜相关。一些细胞区室的膜也有低但显著的标记,特别是高尔基体复合体附近的那些膜。相比之下,抗p14既不标记新月体也不标记IV,但对IV和IMV之间的中间形式有强烈标记,然后与所有后续病毒形式相关。在可识别的细胞膜上也未显著检测到这种蛋白。p32和p14在完整IMV的表面都大量表达。我们的数据与一个模型一致,即p32在被纳入新月体之前会插入细胞膜,而p14会在病毒生命周期的特定后期与病毒外膜进行翻译后结合。