Author: Ãvilaâ€Pérez, Ginés; Rejas, MarÃa Teresa; RodrÃguez, Dolores
Title: Ultrastructural characterization of membranous torovirus replication factories Cord-id: 5psqxxc8 Document date: 2016_7_5
ID: 5psqxxc8
Snippet: Plusâ€stranded RNA viruses replicate in the cytosol of infected cells, in membraneâ€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 doubleâ€membrane vesicles (DMVs) in the cytoplasm of cells infected with the equine to
Document: Plusâ€stranded RNA viruses replicate in the cytosol of infected cells, in membraneâ€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 doubleâ€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 BEVâ€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 doubleâ€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.
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