Ultrastructural characterization of membranous torovirus replication factories

被引:22
作者
Avila-Perez, Gines [1 ]
Teresa Rejas, Maria [2 ]
Rodriguez, Dolores [1 ]
机构
[1] CSIC, Ctr Nacl Biotecnol, Dept Mol & Cellular Biol, C Darwin 3, Madrid 28049, Spain
[2] CSIC, Ctr Biol Mol Severo Ochoa, Electron Microscopy Facil, C Nicolas Cabrera 1, Madrid 28049, Spain
关键词
RESPIRATORY SYNDROME CORONAVIRUS; MOUSE HEPATITIS-VIRUS; DOUBLE-STRANDED-RNA; ENDOPLASMIC-RETICULUM; VIRAL-RNA; BOVINE TOROVIRUS; ARTERIVIRUS NSP4; COLOCALIZATION; PROTEINS; VESICLES;
D O I
10.1111/cmi.12620
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Plus-stranded RNA viruses replicate in the cytosol of infected cells, in membrane-bound replication complexes containing the replicase proteins, the viral RNA and host proteins. The formation of the replication and transcription complexes (RTCs) through the rearrangement of cellular membranes is currently being actively studied for viruses belonging to different viral families. In this work, we identified double-membrane vesicles (DMVs) in the cytoplasm of cells infected with the equine torovirus Berne virus (BEV), the prototype member of the Torovirus genus (Coronaviridae family, Nidovirales order). Using confocal microscopy and transmission electron microscopy, we observed a close relationship between the RTCs and the DMVs of BEV. The examination of BEV-infected cells revealed that the replicase proteins colocalize with each other and with newly synthesized RNA and are associated to the membrane rearrangement induced by BEV. However, the double-stranded RNA, an intermediate of viral replication, is exclusively limited to the interior of DMVs. Our results with BEV resemble those obtained with other related viruses in the Nidovirales order, thus providing new evidence to support the idea that nidoviruses share a common replicative structure based on the DMV arranged clusters.
引用
收藏
页码:1691 / 1708
页数:18
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