Cobbold C, Whittle J T, Wileman T
Division of Immunology, Pirbright Laboratories, Institute for Animal Health, Surrey, United Kingdom.
J Virol. 1996 Dec;70(12):8382-90. doi: 10.1128/JVI.70.12.8382-8390.1996.
African swine fever (ASF) virus is a large enveloped DNA virus assembled in the cytoplasm of cells. In this study, the membrane compartments involved in the envelopment of ASF virus were investigated. A monoclonal antibody recognizing p73, the major structural protein of ASF virus, was generated to analyze the binding of p73 to membranes during the assembly of the virus. Approximately 50% of the intracellular pool of p73 associated with membranes as a peripheral membrane protein. Binding was rapid and complete within 15 min of synthesis. Subcellular membrane fractionation showed that newly synthesized p73 molecules cosedimented with endoplasmic reticulum (ER) membranes and remained associated with the ER during a 2-h chase. A similar distribution on gradients was recorded for p17, a structural membrane protein of ASF virus. The results suggested that the ER was involved in the assembly of ASF virus. A protease protection assay demonstrated a time-dependent envelopment of the membrane bound, but not cytosolic, pool of p73. Envelopment of p73 took place 1 h after binding to membranes and was completed 1 h before the first detection of p73 in virions secreted from cells. Envelopment was unaffected by brefeldin A and monensin, drugs that block membrane transport between the ER and Golgi. Taken together the results provide evidence for the binding of ASF virus structural proteins to a specific membrane compartment and implicate a role for the ER in the assembly and envelopment of ASF virus.
非洲猪瘟(ASF)病毒是一种在细胞质中组装的大型包膜DNA病毒。在本研究中,对参与ASF病毒包膜形成的膜区室进行了研究。制备了一种识别ASF病毒主要结构蛋白p73的单克隆抗体,以分析病毒组装过程中p73与膜的结合情况。约50%的细胞内p73池作为外周膜蛋白与膜结合。合成后15分钟内结合迅速且完全。亚细胞内膜分级分离显示,新合成的p73分子与内质网(ER)膜一起沉降,并在2小时的追踪过程中一直与ER结合。ASF病毒的结构膜蛋白p17在梯度上也有类似的分布。结果表明,ER参与了ASF病毒的组装。蛋白酶保护试验表明,膜结合而非胞质中的p73池存在时间依赖性的包膜化。p73与膜结合1小时后开始包膜化,并在首次在细胞分泌的病毒粒子中检测到p73前1小时完成。包膜化不受布雷菲德菌素A和莫能菌素的影响,这两种药物可阻断ER与高尔基体之间的膜转运。综合这些结果为ASF病毒结构蛋白与特定膜区室的结合提供了证据,并暗示ER在ASF病毒的组装和包膜化过程中发挥作用。