Watermelon chlorotic stunt and Squash leaf curl begomoviruses—New threats to cucurbit crops in the Middle East

References

• Al-Musa, A., Anfoka, G., Misbeh, S., Abhary, M., Ahmad, F. H. 2008. Detection and molecular characterization of Squash leaf curl virus (SLCV) in Jordan. Journal of Phytopathology 156: 311-316.
   Google Scholar
• Antignus, Y., Lachman, O., Pearlsman, M., Omar, S., Yunis, H., Messika, Y., Uko, O., Koren, A. 2003. Squash leaf curl virus—a new illegal immigrant from the Western Hemisphere and a threat to cucurbit crops in Israel. Phytoparasitica 31: 415.
   Google Scholar
• Bananej, K., Ahoonmanesh, A., Kheyr-Pour, A. 2002. Host range of an Iranian isolate of Watermelon chlorotic stunt virus as determined by whitefly-mediated inoculation and agroinfection, and its geographical distribution. Journal of Phytopathology 150: 423-430.
   Google Scholar
• Bedford, I. D., Briddon, R. W., Jones, P., Al-Kaff, N., Markham, P. G. 1994. Differentiation of three whitefly-transmitted geminiviruses from the Republic of Yemen. European Journal of Plant Pathology 100: 243-257.
   Google Scholar
• Bisaro, D. M. 2006. Silencing suppression by geminivirus proteins. Virology 344: 158-168.
   Google Scholar
• Brown, J. K., Frohlich, D. R., Rosell, R. C. 1995. The sweetpotato or silverleaf whiteflies: biotypes of Bemisia tabaci or a species complex? Annual Review of Entomology 40: 511-669.
   Google Scholar
• Brown, J. K., Idris, A. M., Rogan, D., Hussein, M. H., Palmieri, M. 2001. Melon chlorotic leaf curl virus, a new begomovirus associated with Bemisia tabaci infestations in Guatemala. Plant Disease 85: 1027.
   Google Scholar
• Brown, J. K., Idris, A. M., Alteri, C., Stenger, D. C. 2002. Emergence of a new cucurbit-infecting begomovirus species capable of forming viable reassortments with related viruses in the squash leaf curl virus cluster. Phytopathology 92: 734-742.
   Google Scholar
• Brown, J., Baumann, K., Idris, A. 2005. Characterization of squash leaf curl and squash mild leaf curl viruses: host range and reassortment for four SLCV clade viruses. Phytopathology 95: S14.
   Google Scholar
• Carvalho, C. M., Lazarowitz, S. G. 2004. Interaction of the movement protein NSP and the Arabidopsis acetyltransferase AtNSI is necessary for cabbage leaf curl geminivirus infection and pathogenicity. Journal of Virology 78: 11161-11171.
   Google Scholar
• Cohen, S., Duffus, J. E., Larsen, R. C., Liu, H. Y., Flock, R. A. 1983. Purification, serology, and vector relationships of squash leaf curl virus, a whitefly-transmitted geminivirus. Phytopathology 73: 1669-1673.
   Google Scholar
• Dellaporta, S. L., Wood, J., Hicks, J. B. 1983. Maize DNA miniprep. Plant Molecular Biology Reporter 1: 19-21.
   Google Scholar
• Fauquet, C. M., Stanley, J. 2005. Revising the way we conceive and name viruses below the species level: a review of geminivirus taxonomy calls for new standardized isolate descriptors. Archives of Virology 150: 2151-2179.
   Google Scholar
• Fauquet, C. M., Briddon, R.W, Brown, J.K, Moriones, E, Stanley, J, Zerbini, M, Zhou, X. 2008. Geminivirus strain demarcation and nomenclature. Archives of Virology 153: 783-821.
   Google Scholar
• Finer, J. J., Vain, P., Jones, M. W., McMullen, D. 1992. Development of the particle inflowgun for DNA delivery to plant cells. Plant Cell Reports 11: 323-328.
   Google Scholar
• Flock, R. A., Mayhew, D. E. 1981. Squash leaf curl, a new disease of cucurbits in California. Plant Disease 65: 75-76.
   Google Scholar
• Gaba, V., Gal-On, A. 2005. Inoculation of plants using bombardment. In: Simon, A., Kowalik, T., Quarles, J., eds. Current protocols in microbiology. Wiley Interscience, pp. Unit 16B.13.11-16B.13.14.
   Google Scholar
• Gutierrez, C. 2002. Strategies for geminivirus DNA replication and cell cycle interference. Physiological and Molecular Plant Pathology 60: 219-230.
   Google Scholar
• Hanley-Bowdoin, L., Settlage, S. B., Orozco, B. M., Nagar, S., Robertson, D. 1999. Geminiviruses: models for plant DNA replication, transcription, and cell cycle regulation. Critical Reviews in Plant Sciences 18: 71-106.
   Google Scholar
• Hanley-Bowdoin, L., Settlage, S. B., Robertson, D. 2004. Reprogramming plant gene expression: a prerequisite to geminivirus DNA replication. Molecular Plant Pathology 5: 149-156.
   Google Scholar
• Idris, A. M., Abdel-Salam, A., Brown, J. K. 2006. Introduction of the new world Squash leaf curl virus to squash (Cucurbita pepo) in Egypt: a potential threat to important food crops. Plant Disease 90: 1262
   Google Scholar
• Ingham, D. J., 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.
   Google Scholar
• Ingham, D. J., Pascal, E., Lazarowitz, S. G. 1995. Both Bipartite geminivirus movement proteins define viral host-range, but only Bl1 determines viral pathogenicity. Virology 207: 191-204.
   Google Scholar
• Jones, D. R. 2003. Plant viruses transmitted by whiteflies. European Journal of Plant Pathology 109: 195-219.
   Google Scholar
• Jones, P., Sattar, M. H. A., Al-Kaff, N. 1988. The incidence of virus disease in watermelon and sweet melon crops in the Peoples Republic of Yemen and its impact on cropping policy. Aspects of Applied Biology 17: 203-207.
   Google Scholar
• Kheyr-Pour, A., Bananej, K., Dafalla, G. A., Caciagli, P., Noris, E., Ahoonmanesh, A., Lecoq, H., Gronenborn, B. 2000. Watermelon chlorotic stunt virus from the Sudan and Iran: sequence comparisons and identification of a whitefly-transmission determinant. Phytopathology 90: 629-635.
   Google Scholar
• Lapidot, M., Friedmann, M. 2002. Breeding for resistance to whitefly-transmitted geminiviruses. Annals of Applied Biology 140: 109-127.
   Google Scholar
• Lapidot, M., Weil, G., Cohen, L., Segev, L., Gaba, V. 2007. Biolistic inoculation of plants with Tomato yellow leaf curl virus DNA. Journal of Virological Methods 144: 143-148.
   Google Scholar
• 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.
   Google Scholar
• Lazarowitz, S. G., Beachy, R. N. 1999. Viral movement proteins as probes for intracellular and intercellular trafficking in plants. Plant Cell 11: 535-548.
   Google Scholar
• Mansoor, S., Briddon, R. W., Zafar, Y., Stanley, J. 2003. Geminivirus disease complexes: an emerging threat. Trends in Plant Science 8: 128-134.
   Google Scholar
• Rojas, M. R., Gilbertson, R. L., Russell, D. R., Maxwell, D. P. 1993. Use of degenerate primers in the polymerase chain reaction to detect whitefly-transmitted geminiviruses. Plant Disease 77: 340-347.
   Google Scholar
• Rosemeyer, M. E., Brown, J. K., Nelson, M. R. 1986. Five viruses isolated from field-grown buffalo gouard (Cucurbita foetidissima), a potential crop for semiarid lands. Plant Disease 70: 405-409.
   Google Scholar
• Sanderfoot, A. A., Ingham, D. J., Lazarowitz, S. G. 1996. A viral movement protein as a nuclear shuttle. The geminivirus BR1 movement protein contains domains essential for interaction with BL1 and nuclear localization. Plant Physiology 110: 23-33.
   Google Scholar
• Sufrin-Ringwald, T. 2008. Molecular identification and characterization of the interaction between two geminiviruses: Squash leaf curl virus (SLCV) and Watermelon chlorotic stunt virus (WmCSV). M. Sc thesis, Hebrew Univ., Jerusalem.
   Google Scholar
• Varma, A., Malathi, V. G. 2003. Emerging geminivirus problems: a serious threat to crop production. Annals of Applied Biology 142: 145-164.
   Google Scholar
• Walkey, D. G. A., Alhubaishi, A. A., Webb, M. J. W. 1990. Plant virus diseases in the Yemen Arab Republic. Tropical Pest Management 36: 195-206.
   Google Scholar
• Yousif, M, T., Kheyr-Pour, A., Gronenborn, B., Pitrat, M., Dogimont, C. 2007. Sources of resistance to Watermelon Chlorotic Stunt Virus in melon. Plant Breeding 126: 422-427.
   Google Scholar