Williams O, Wolffe E J, Weisberg A S, Merchlinsky M
Laboratory of Viral Diseases, Center for Biologics Evaluation and Research, Food and Drug Administration, Rockville, Maryland 20852, USA.
J Virol. 1999 Jun;73(6):4590-9. doi: 10.1128/JVI.73.6.4590-4599.1999.
The vaccinia virus WR A5L open reading frame (corresponding to open reading frame A4L in vaccinia virus Copenhagen) encodes an immunodominant late protein found in the core of the vaccinia virion. To investigate the role of this protein in vaccinia virus replication, we have constructed a recombinant virus, vA5Li, in which the endogenous gene has been deleted and an inducible copy of the A5 gene dependent on isopropyl-beta-D-thiogalactopyranoside (IPTG) for expression has been inserted into the genome. In the absence of inducer, the yield of infectious virus was dramatically reduced. However, DNA synthesis and processing, viral protein expression (except for A5), and early stages in virion formation were indistinguishable from the analogous steps in a normal infection. Electron microscopy revealed that the major vaccinia virus structural form present in cells infected with vA5Li in the absence of inducer was immature virions. Viral particles were purified from vA5Li-infected cells in the presence and absence of inducer. Both particles contained viral DNA and the full complement of viral proteins, except for A5, which was missing from particles prepared in the absence of inducer. The particles prepared in the presence of IPTG were more infectious than those prepared in its absence. The A5 protein appears to be required for the immature virion to form the brick-shaped intracellular mature virion.
痘苗病毒WR株的A5L开放阅读框(对应于痘苗病毒哥本哈根株的开放阅读框A4L)编码一种在痘苗病毒粒子核心中发现的免疫显性晚期蛋白。为了研究该蛋白在痘苗病毒复制中的作用,我们构建了一种重组病毒vA5Li,其中内源性基因已被删除,并且将一个依赖异丙基-β-D-硫代半乳糖苷(IPTG)表达的A5基因诱导型拷贝插入到基因组中。在没有诱导剂的情况下,感染性病毒的产量显著降低。然而,DNA合成与加工、病毒蛋白表达(除A5外)以及病毒粒子形成的早期阶段与正常感染中的类似步骤并无差异。电子显微镜显示,在没有诱导剂的情况下感染vA5Li的细胞中存在的主要痘苗病毒结构形式是未成熟病毒粒子。在有和没有诱导剂的情况下,从感染vA5Li的细胞中纯化病毒粒子。两种粒子都含有病毒DNA和除A5外的完整病毒蛋白,在没有诱导剂的情况下制备的粒子中缺少A5。在IPTG存在下制备的粒子比在其不存在时制备的粒子更具感染性。A5蛋白似乎是未成熟病毒粒子形成砖形细胞内成熟病毒粒子所必需的。