Host range limitation of a pseudorecombinant virus produced by two distinct bipartite geminiviruses

Molecular Plant-Microbe Interactions

Volumn 10, Issue 8, 1997, Pages 1019-1022

  Höfer, Petra ^a   Engel, Margit ^a   Jeske, Holger ^a   Frischmuth, Thomas ^a  

^a UNIVERSITY OF STUTTGART   (Germany)

Author keywords

Pseudorecombination; Trans replication

Indexed keywords

ABUTILON; ABUTILON MOSAIC VIRUS; SIDA GOLDEN MOSAIC VIRUS;

EID: 1842298694     PISSN: 08940282     EISSN: None     Source Type: Journal    
DOI: 10.1094/MPMI.1997.10.8.1019     Document Type: Article

References (30)

1. Abouzid, A. M., Polston, J. E., and Hiebert, E. 1992. The nucleotide sequence of tomato mottle virus, a new geminivirus isolated from tomatoes in Florida. J. Gen. Virol. 73:3225-3229.
2. Buragohain, A. K., Sung, Y. K., Coffin, R. S., and Coutts, R. H. A. 1994. The infectivity of dimeric potato yellow mosaic geminivirus clones in different hosts. J. Gen. Virol. 75:2857-2861.
3. Coutts, R. H. A., Coffin, R. S., Roberts, E. J. F., and Hamilton, W. D. O. 1991. The nucleotide sequence of the infectious cloned DNA components of potato yellow mosaic virus. J. Gen. Virol. 72:1515-1520.
4. Evans, D., and Jeske, H. 1993. DNA B facilitates, but is not essential for, the spread of Abutilon mosaic virus in agroinoculated Nicotiana benthamiana. Virology 194:752-757.
5. Fontes, E. P. B., Eagle, P., Sipe, P., Luckow, V. A., and Hanley-Bowdoin, L. 1994a. Interaction between a geminivirus replication protein and origin DNA is essential for viral replication. J. Biol. Chem. 269:8459-8465.
6. Fontes, E. P. B., Gladfelter, H. J., Schaffer, R. L., Petty, I. T. D., and Hanley-Bowdoin, L. 1994b. Geminivirus replication origins have a modular organization. Plant Cell 6:405-416.
7. Frischmuth, T., Roberts, S., von Arnim, A., and Stanley, J. 1993. Specificity of bipartite geminivirus movement proteins. Virology 196:666-673.
8. Frischmuth, T., and Stanley, J. 1991. African cassava mosaic virus DI DNA interferes with the replication of both genomic components. Virology 183:539-544.
9. Frischmuth, T., Zimmat, G., and Jeske, H. 1990. The nucleotide sequence of Abutilon mosaic virus reveals prokaryotic as well as eukaryotic features. Virology 178:461-468.
10. Gilbertson, R. L., Hidayat, S. H., Paplomatas, E. J., Rojas, M. R., Hou, Y.-M., and Maxwell, D. P. 1993. Pseudorecombination between infectious cloned DNA components of tomato mottle and bean dwarf mosaic geminiviruses. J. Gen. Virol. 74:23-31.
11. Harrison, B. D. 1985. Advances in geminivirus research. Annu. Rev. Phytopathol. 23:55-82.
12. Hidayat, S. H., Gilbertson, R. L., Hanson, S. F., Morales, F. J., Ahlquist, P., Russell, D. R., and Maxwell D. P. 1993. Complete nucleotide sequences of the infectious cloned DNAs of bean dwarf mosaic geminivirus. Phytopathology 83:181-187.
13. Höfer, P., Engel, M., Jeske, H., and Frischmuth, T. 1997. Nucleotide sequence of a new bipartite geminivirus isolated from the common weed Sida rhombifolia in Costa Rica. J. Gen. Virol. 78:1785-1790.
14. Hou, Y.-M., and Gilbertson R. L. 1996. Increased pathogenicity in a pseudorecombinant bipartite geminivirus correlates with intermolecular recombination. J. Virol. 70:5430-5436.
15. Ingham, D. J., and Lazarowitz, S. G. 1993. A single missense mutation in the BR1 movement protein alters the host range of the squash leaf curl geminivirus. Virology 196:694-702.
16. Ingham, D. J., Pascal, E., and Lazarowitz, S. G. 1995. Both bipartite geminivirus movement proteins define viral host range, but only BL1 determines viral pathogenicity. Virology 20:7191-204.
17. Klinkenberg, F. A., and Stanley, J. 1990. Encapsidation and spread of African cassava mosaic virus DNA A in the absence of DNA B when agroinoculated to Nicotiana benthamiana. J. Gen. Virol. 71:1409-1412.
18. Lazarowitz, S. G. 1991. Molecular characterization of two bipartite geminiviruses causing squash leaf curl disease: Role of viral replication and movement functions in determining host range. Virology 180:70-80.
19. Lazarowitz, S. G. 1992. Geminiviruses: Genome structure and gene function. Crit. Rev. Plant Sci. 11:327-349.
20. Murphy, F. A., Fauquet, C. M., Bishop, D. H. L., Ghabrial, S. A., Jarvis, A. W., Martelli, G. P., Mayo, M. A., and Summers, M. D. 1995. Virus taxonomy. Arch. Virol. Suppl. 10:158-165.
21. Noueiry, A. O., Lucas, W. J., and Gilbertson, R. L. 1994. Two proteins of a plant DNA virus coordinate nuclear and plasmodesmal transport. Cell 76:925-932.
22. Sanderfoot, A. A., and Lazarowitz, S. G. 1995. Cooperation in viral movement: The geminivirus BL1 movement protein interacts with BR1 and redirects it from the nucleus to the cell periphery. Plant Cell 7:1185-1194.
23. Schaffer, R. L., Miller, C. G., and Petty, I. T. D. 1995. Virus and host-specific adaptations in the BL1 and BR1 genes of bipartite geminiviruses. Virology 214:330-338.
24. Stanley, J., Frischmuth, T., and Ellwood, S. 1990. Defective viral DNA ameliorates symptoms of geminiviruses infection in transgenic plants. Proc. Natl. Acad. Sci. USA 87:6291-6295.
25. Stanley, J., Townsend, R., and Curson, S. J. 1985. Pseudorecombinants between cloned DNAs of two isolates of cassava latent virus. J. Gen. Virol. 66:1055-1061.
26. Stenger, D. C., Davis, K. R., and Bisaro, D. M. 1994. Recombinant beet curly top virus genomes exhibit both parental and novel phenotypes. Virology 200:677-685.
27. Sung, Y. K., and Coutts, R. H. A. 1995a. Mutational analysis of potato yellow mosaic geminivirus. J. Gen. Virol. 76:1773-1780.
28. Sung, Y. K., and Coutts, R. H. A. 1995b. Pseudorecombination and complementation between potato yellow mosaic geminivirus and tomato golden mosaic geminivirus. J. Gen. Virol. 76:2809-2815.
29. Timmermans, M. C. P., Das, O. P., and Messing, J. 1994. Geminiviruses and their uses as extrachromosomal replicons. Annu. Rev. Plant Physiol. Plant Mol. Biol. 45:79-112.
30. von Amim, A., and Stanley, J. 1992. Determinants of tomato golden mosaic virus symptom development located on DNA B. Virology 186: 286-293.