A guide to viral inclusions, membrane rearrangements, factories, and viroplasm produced during virus replication

被引:167
作者
Netherton, Christopher [1 ]
Moffat, Katy
Brooks, Elizabeth
Wileman, Thomas
机构
[1] Inst Anim Hlth, Pirbright Labs, Vaccinol Grp, Surrey, England
[2] Univ E Anglia, Fac Hlth, Sch Med, Norwich NR4 7TJ, Norfolk, England
来源
ADVANCES IN VIRUS RESEARCH, VOL 70 | 2007年 / 70卷
关键词
SWINE-FEVER VIRUS; HEPATITIS-C VIRUS; DOUBLE-STRANDED-RNA; PROMYELOCYTIC LEUKEMIA PROTEIN; DNA-BINDING PROTEIN; TRANS-GOLGI NETWORK; REOVIRUS SIGMA-NS; NUCLEAR DOMAIN 10; A-TYPE INCLUSION; TYPE-1 PREREPLICATIVE SITES;
D O I
10.1016/S0065-3527(07)70004-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Virus replication can cause extensive rearrangement of host cell cytoskeletal and membrane compartments leading to the "cyto-pathic effect" that has been the hallmark of virus infection in tissue culture for many years. Recent studies are beginning to redefine these signs of viral infection in terms of specific effects of viruses on cellular processes. in this chapter, these concepts have been illustrated by describing the replication sites produced by many different viruses. In many cases, the cellular rearrangements caused during virus infection lead to the construction of sophisticated platforms in the cell that concentrate replicase proteins, virus genomes, and host proteins required for replication, and thereby increase the efficiency of replication. Interestingly, these same structures, called virus factories, virus inclusions, or virosomes, can recruit host components that are associated with cellular defences against infection and cell stress. it is possible that cellular defence pathways can be subverted by viruses to generate sites of replication. The recruitment of cellular membranes and cytoskeleton to generate virus replication sites can also benefit viruses in other ways. Disruption of cellular membranes can, for example, slow the transport of immunomodulatory proteins to the surface of infected cells and protect against innate and acquired immune responses, and rearrangements to cytoskeleton can facilitate virus release.
引用
收藏
页码:101 / 182
页数:82
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