The ORF3-encoded proteins of vitiviruses GVA and GVB induce tubule-like and punctate structures during virus infection and localize to the plasmodesmata

Sabrina Haviv, Yoni Moskovitz, Munir Mawassi

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

The genomic RNA of vitiviruses contains 5 open reading frames (ORF). ORF3 encodes a protein to which the function of a movement protein (MP) was assigned, based on sequence homology with other viral proteins. The aim of the research described in this paper was to gain further insight in distribution profile of the ORF3 product encoded by the vitiviruses Grapevine virus A (GVA) and Grapevine virus B (GVB). Expression of the GVA MP-GFP fusion protein via the virus genome in Nicotiana benthamiana leaves resulted in the formation of irregular spots and fibrous network structures on the outermost periphery of epidermal cells. Expression of GVA MP-GFP and GVB MP-GFP was involved in the formation of the tubule-like and punctate structures on the periphery of N. benthamiana and Vitis vinifera protoplasts. Co-expression of the GVA MP-GFP and GVA MP-RFP in protoplasts resulted in co-localization of these proteins into the same punctate structures, indicating that the MP is not accumulated randomly onto the cell surface, but targeted to particular sites at the cell periphery, where punctate and tubule-like structures are likely formed. With the use of cytoskeleton and secretory pathway inhibitors, we showed that the cytoskeletal elements are not likely to be involved in targeting of the MP-GFP to the punctate cellular structures. In addition to MP, a functional coat protein was found to be essential for virus spread within inoculated leaves.

Original languageEnglish
Pages (from-to)291-301
Number of pages11
JournalVirus Research
Volume163
Issue number1
DOIs
StatePublished - Jan 2012
Externally publishedYes

Bibliographical note

Funding Information:
The authors are grateful to Dr. Victor Gaba for critical reading of the manuscript. We thank Dr. Joan Wellink (Wageningen University, Laboratory of Molecular Biology, 6703 HA Wageningen. The Netherlands) for pMON-YFP-Talin and pUC-GFP-MBD, which were used as templates for PCR amplification of YFP-Talin and GFP-MBD, respectively. We also thank Dr Bernard L. Epel (Tel Aviv University, Department of Plant Sciences, George S Wise Faculty of Life Sciences, Tel Aviv, Israel) for providing the clone TMV-MP-YFP. Thanks to Dr Tzvi Tzfira (University of Michigan, Department of Molecular, Cellular and Developmental Biology, MI, United States) as well as to Dr Yedidya Gafni (ARO, The Volcani Center, Institute of Plant Sciences, Bet Dagan, Israel) for providing the templates which used for PCR amplification of the RFP, YFP and CFP sequences. This research was supported by research grant No. IS-4314-10C from BARD, the United States-Israel Binational Agricultural Research and Development Fund ; and by grant no. 565/05 from the Israeli Science Foundation.

Funding

The authors are grateful to Dr. Victor Gaba for critical reading of the manuscript. We thank Dr. Joan Wellink (Wageningen University, Laboratory of Molecular Biology, 6703 HA Wageningen. The Netherlands) for pMON-YFP-Talin and pUC-GFP-MBD, which were used as templates for PCR amplification of YFP-Talin and GFP-MBD, respectively. We also thank Dr Bernard L. Epel (Tel Aviv University, Department of Plant Sciences, George S Wise Faculty of Life Sciences, Tel Aviv, Israel) for providing the clone TMV-MP-YFP. Thanks to Dr Tzvi Tzfira (University of Michigan, Department of Molecular, Cellular and Developmental Biology, MI, United States) as well as to Dr Yedidya Gafni (ARO, The Volcani Center, Institute of Plant Sciences, Bet Dagan, Israel) for providing the templates which used for PCR amplification of the RFP, YFP and CFP sequences. This research was supported by research grant No. IS-4314-10C from BARD, the United States-Israel Binational Agricultural Research and Development Fund ; and by grant no. 565/05 from the Israeli Science Foundation.

FundersFunder number
United States - Israel Binational Agricultural Research and Development Fund565/05
BARD
Israel Science Foundation

    Keywords

    • GFP
    • Grapevine viruses
    • Movement protein
    • Protoplasts
    • Vitiviruses

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