Heath C M, Windsor M, Wileman T
Institute for Animal Health, Pirbright Laboratories, Surrey GU24 0NF, United Kingdom.
J Cell Biol. 2001 Apr 30;153(3):449-55. doi: 10.1083/jcb.153.3.449.
The large cytoplasmic DNA viruses such as poxviruses, iridoviruses, and African swine fever virus (ASFV) assemble in discrete perinuclear foci called viral factories. Factories exclude host proteins, suggesting that they are novel subcellular structures induced by viruses. Novel perinuclear structures, called aggresomes are also formed by cells in response to misfolded protein (Johnston, J.A., C.L. Ward, and R.R. Kopito. 1998. J. Cell Biol. 143:1883--1898; García-Mata, R., Z. Bebök, E.J. Sorscher, and E.S. Sztul. 1999. J. Cell Biol. 146:1239--1254). In this study, we have investigated whether aggresomes and viral factories are related structures. Aggresomes were compared with viral factories produced by ASFV. Aggresomes and viral factories were located close to the microtubule organizing center and required an intact microtubular network for assembly. Both structures caused rearrangement of intermediate filaments and the collapse of vimentin into characteristic cages, and both recruited mitochondria and cellular chaperones. Given that ASFV factories resemble aggresomes, it is possible that a cellular response originally designed to reduce the toxicity of misfolded proteins is exploited by cytoplasmic DNA viruses to concentrate structural proteins at virus assembly sites.
大型细胞质DNA病毒,如痘病毒、虹彩病毒和非洲猪瘟病毒(ASFV),在称为病毒工厂的离散核周病灶中组装。病毒工厂排除宿主蛋白,这表明它们是病毒诱导的新型亚细胞结构。细胞也会因错误折叠的蛋白质而形成称为聚集体的新型核周结构(约翰斯顿,J.A.,C.L.沃德,和R.R.科皮托。1998年。《细胞生物学杂志》143:1883 - 1898;加西亚 - 马塔,R.,Z.贝博克,E.J.索尔舍尔,和E.S.斯图尔。1999年。《细胞生物学杂志》146:1239 - 1254)。在本研究中,我们调查了聚集体和病毒工厂是否为相关结构。将聚集体与ASFV产生的病毒工厂进行了比较。聚集体和病毒工厂都位于靠近微管组织中心的位置,并且组装需要完整的微管网络。这两种结构都会导致中间丝重排以及波形蛋白塌陷成特征性的笼状结构,并且都会募集线粒体和细胞伴侣蛋白。鉴于ASFV工厂类似于聚集体,细胞质DNA病毒有可能利用原本设计用于降低错误折叠蛋白毒性的细胞反应,将结构蛋白集中在病毒组装位点。