Infection by Grapevine fanleaf nepovirus (GFLV), a bipartite RNA virus of positive polarity belonging to the Comoviridae family, causes extensive cytopathic. The specific transmission of Grapevine fanleaf virus by its nematode vector Xiphinema index is solely determined by the viral coat protein. There are plenty of plant viruses that no one has heard of, but few are as widely known as grapevine fanleaf virus. Learn how to identify a sick.
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In the case of poliovirus, it was shown that specific viral proteins were responsible for vesicle formation 6762 and that formation of the poliovirus replication complex is a process that requires coupled viral translation, vesicle production, and viral RNA synthesis Immunolabeling of viral proteins.
Virks localization of the peanut clump virus replication complex in tobacco-BY-2 protoplasts containing GFP-labeled endoplasmic rgapevine or Golgi apparatus. Effects of site-directed mutagenesis on the presumed catalytic triad and substrate-binding pocket of grapevine fanleaf nepovirus kDa proteinase.
In an attempt to visualize the membranes that cosedimented with the VPg precursors, ISEM was performed on sucrose gradient fractions with fanlwaf anti-VPg antibodies. Fruit clusters are reduced in size and number with irregular ripening. Finally, coat protein was also sometimes observed within the nucleoplasm Fig.
Fanleaf Degeneration of Grape
These spots were always restricted to the VPg-labeled areas in the nuclear periphery Fig. The rooting ability of rootstocks and the graft take of scions are both substantially reduced in grapevine fanleaf virus GFLV -infected material. For FDA, the parameters were as follows: Further in vivo time course analysis will be required to confirm the observed variations in the number of Golgi stacks within a single cell during the course of infection, but this is beyond the scope of this study.
Similarity in gene organization and homology between proteins of animal picornaviruses and a plant comovirus suggest common ancestry of these virus families. Napier Warwick, United Kingdomand J. No significant signal was observed in similarly processed healthy protoplasts Fig.
Grapevine Fanleaf Degeneration Disease
The fixative was replaced by 2. Fanleaf DegenerationCornell University. Detection of viral proteins in cytopathic structures in cowpea protoplasts infected with cowpea mosaic virus.
Affected vines show chrome-yellow discolorations that develop early in the spring and may affect all vegetative parts of the vines. These observations imply that GFLV replication depends both on ER-derived membrane recruitment and on de novo lipid synthesis. Characterization of rubella virus replication complexes using antibodies to double-stranded RNA.
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RNA1 encodes polyprotein P1 kDawhich is processed by an embedded proteinase activity into five proteins required for replication, namely, 1A of unknown function1B probably the helicase1C VPg1D proteinaseand 1E polymerase 38 Interaction of Theiler’s virus with intermediate filaments of infected cells.
In view of the close resemblance between both systems, we suggest that GFLV could use a similar mechanism to recruit membranes for replication purposes. Inhibition of Golgi apparatus function by brefeldin A in maize coleoptiles and its consequences on auxin mediated growth, cell wall extensibility, and secretion of cell wall proteins.
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Arrowheads, Golgi; N, nucleus; P, plastids; M, mitochondria. Michler for technical assistance in electron microscopy. Remodeling the endoplasmic reticulum by poliovirus infection and by individual viral proteins: A modified form of the alfalfa mosaic virus movement protein induces stressed phenotypes in transgenic tobacco.
Grapevine fanleaf degeneration disease is caused by the grapevine fanleaf virus Fanlewfa member of the nepovirus group.
Grapevine Fanleaf Virus Replication Occurs on Endoplasmic Reticulum-Derived Membranes
Immunocytochemical localization of TYMV-coded structural and non-structural proteins by the protein A-gold technique. Tobacco mosaic virus infection induces severe morphological changes of the garpevine reticulum.
To further refine the analysis of GFLV replication sites, the grapevins organization of the perinuclear aggregates containing the viral products was studied by electron microscopy on infected protoplasts Fig. Conventional and high voltage electron microscopy of the cytoskeleton and cytoplasmic matrix of carrot Daucus carota L.