Grapevine Fanleaf Virus Replication Occurs on Endoplasmic Reticulum-Derived Membranes

Author:

Ritzenthaler C.1,Laporte C.1,Gaire F.1,Dunoyer P.1,Schmitt C.1,Duval S.1,Piéquet A.1,Loudes A. M.1,Rohfritsch O.1,Stussi-Garaud C.1,Pfeiffer P.1

Affiliation:

1. Institut de Biologie Moléculaire des Plantes, 67084 Strasbourg Cedex, France

Abstract

ABSTRACT Infection by Grapevine fanleaf nepovirus (GFLV), a bipartite RNA virus of positive polarity belonging to the Comoviridae family, causes extensive cytopathic modifications of the host endomembrane system that eventually culminate in the formation of a perinuclear “viral compartment.” We identified by immunoconfocal microscopy this compartment as the site of virus replication since it contained the RNA1-encoded proteins necessary for replication, newly synthesized viral RNA, and double-stranded replicative forms. In addition, by using transgenic T-BY2 protoplasts expressing green fluorescent protein in the endoplasmic reticulum (ER) or in the Golgi apparatus (GA), we could directly show that GFLV replication induced a depletion of the cortical ER, together with a condensation and redistribution of ER-derived membranes, to generate the viral compartment. Brefeldin A, a drug known to inhibit vesicle trafficking between the GA and the ER, was found to inhibit GFLV replication. Cerulenin, a drug inhibiting de novo synthesis of phospholipids, also inhibited GFLV replication. These observations imply that GFLV replication depends both on ER-derived membrane recruitment and on de novo lipid synthesis. In contrast to proteins involved in viral replication, the 2B movement protein and, to a lesser extent, the 2C coat protein were not confined to the viral compartment but were transported toward the cell periphery, a finding consistent with their role in cell-to-cell movement of virus particles.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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