Origins of membrane vesicles generated during replication of positive-strand RNA viruses

被引:14
作者
Cottam, Eleanor [1 ]
Pierini, Roberto [1 ]
Roberts, Rebecca [1 ]
Wileman, Thomas [1 ]
机构
[1] Univ E Anglia, Inst Biomed & Clin Sci, Sch Med, Norwich NR4 7TJ, Norfolk, England
基金
英国生物技术与生命科学研究理事会;
关键词
Arf GTPase; autophagy; double-membraned vesicles; membrane traffic; positive-strand RNA virus; spherules; tomography; MOUTH-DISEASE VIRUS; COXSACKIEVIRUS 2B PROTEIN; EARLY SECRETORY PATHWAY; HOST-CELL MEMBRANES; CORONAVIRUS REPLICATION; ENDOPLASMIC-RETICULUM; POLIOVIRUS INFECTION; GOLGI TRAFFICKING; COMPLEX; AUTOPHAGY;
D O I
10.2217/FVL.09.26
中图分类号
Q93 [微生物学];
学科分类号
071005 [微生物学];
摘要
Infection of cells by positive-strand RNA viruses generates large numbers of membrane vesicles that provide sites for genome replication. Vesicle formation is initiated by targeting replicase proteins to the cytosolic face of membrane-bound organelles where protein assembly induces membrane curvature. This can result in invagination into the limiting membrane of membrane compartments or induce vesicle budding into the cytoplasm. The new membranes are thought to provide a platform to concentrate proteins, lipids and nucleotides that are required for genome replication. This article describes how recent advances in cell biology and cellular imaging can reveal these structures in 3D, and begin to define how they are formed terms of effects of specific viral proteins on specific cellular processes.
引用
收藏
页码:473 / 485
页数:13
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