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5’ Proximal potyviral sequences mediate potato virus X/potyviral synergistic disease in transgenic tobacco

  • Vicki Bowman Vance
  • , Philip H. Berger
  • , James C. Carrington
  • , Arthur G. Hunt
  • , Xing Ming Shi

Producción científica: Article › revisión exhaustiva

153 Citas (Scopus)

Resumen

The interaction of potato virus X (PVX) and potato virus Y (PVY) in tobacco causes a synergistic disease characterizedby a dramatic increase in symptom severity, a change in the regulation of PVX RNA replication, and an increase in accumulation of PVX. In this study we demonstrate that PVX also interacts synergistically with three other members of the potyvirus group of plant viruses, tobacco vein mottling virus (TVMV), tobacco etch virus (TEV), and pepper mottle virus. These synergisms resemble the classic PVX/PVY synergism with respect to both the increase in host response and the change in PVX replication. To determine if the induction of PVX/potyviral synergism requires potyviral genome replication per se or if the response is mediated by expression of one or more potyviral genes, we used tobacco plants stably transformed with various subsets of the TVMV genome. PVX infections of transgenic plants expressing the 5′-proximal region of the TVMV genome, including the protease-1, helper component protease, and protein-3 genes, result in symptoms resembling those of PVX/potyviral synergism. A similar synergistic-like response occurs when transgenic tobacco plants expressing the analogous but smaller region from the 5′-proximal region of the TEV genome were infected with PVX. Replication of PVX RNA is altered in transgenic plants expressing 5′-proximal sequences of either TVMV or TEV, and in a manner similar to that observed in double infections. These results indicate that replication of the potyviral genome is not required for PVX/potyviral synergism and that the response is mediated by expression of potyviral sequences which have been localized to the 5′-proximal third of the genomic RNAs of both TVMV and TEV.

Idioma originalEnglish
Número de artículo95800751
Páginas (desde-hasta)583-590
Número de páginas8
PublicaciónVirology
Volumen206
N.º1
DOI
EstadoPublished - ene 10 1995

Nota bibliográfica

Funding Information:
The authors gratefully acknowledge Drs. Lewis Bowman and Gall Pruss for critical reading of the manuscript and helpful discussions. This work was supported by Grant DBM-9223273 from the National Science Foundation and Grant 9304447 from the USDA Biotechnology Risk Assessment Program.

Financiación

The authors gratefully acknowledge Drs. Lewis Bowman and Gall Pruss for critical reading of the manuscript and helpful discussions. This work was supported by Grant DBM-9223273 from the National Science Foundation and Grant 9304447 from the USDA Biotechnology Risk Assessment Program.

FinanciadoresNúmero del financiador
National Science Foundation (NSF)
Directorate for Biological Sciences9223273, 9304447
U.S. Department of Agriculture

    ASJC Scopus subject areas

    • Virology

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