Three-Dimensional Architecture and Biogenesis of Membrane Structures Associated with Hepatitis C Virus Replication

Inés Romero‐Brey(Heidelberg University), Andreas Merz(Heidelberg University), Abhilash I. Chiramel(Heidelberg University), Ji‐Young Lee(Heidelberg University), Petr Chlanda(European Molecular Biology Laboratory), Uta Haselman(European Molecular Biology Laboratory), Rachel Santarella‐Mellwig(European Molecular Biology Laboratory), Anja Habermann(Heidelberg University), Simone Hoppe(Heidelberg University), Stephanie Kallis(Heidelberg University), Paul Walther(Universität Ulm), Claude Antony(European Molecular Biology Laboratory), Jacomine Krijnse‐Locker(Heidelberg University), Ralf Bartenschlager(Heidelberg University)
PLoS Pathogens
December 6, 2012
Cited by 514Open Access
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Abstract

All positive strand RNA viruses are known to replicate their genomes in close association with intracellular membranes. In case of the hepatitis C virus (HCV), a member of the family Flaviviridae, infected cells contain accumulations of vesicles forming a membranous web (MW) that is thought to be the site of viral RNA replication. However, little is known about the biogenesis and three-dimensional structure of the MW. In this study we used a combination of immunofluorescence- and electron microscopy (EM)-based methods to analyze the membranous structures induced by HCV in infected cells. We found that the MW is derived primarily from the endoplasmic reticulum (ER) and contains markers of rough ER as well as markers of early and late endosomes, COP vesicles, mitochondria and lipid droplets (LDs). The main constituents of the MW are single and double membrane vesicles (DMVs). The latter predominate and the kinetic of their appearance correlates with kinetics of viral RNA replication. DMVs are induced primarily by NS5A whereas NS4B induces single membrane vesicles arguing that MW formation requires the concerted action of several HCV replicase proteins. Three-dimensional reconstructions identify DMVs as protrusions from the ER membrane into the cytosol, frequently connected to the ER membrane via a neck-like structure. In addition, late in infection multi-membrane vesicles become evident, presumably as a result of a stress-induced reaction. Thus, the morphology of the membranous rearrangements induced in HCV-infected cells resemble those of the unrelated picorna-, corona- and arteriviruses, but are clearly distinct from those of the closely related flaviviruses. These results reveal unexpected similarities between HCV and distantly related positive-strand RNA viruses presumably reflecting similarities in cellular pathways exploited by these viruses to establish their membranous replication factories.


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