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In Jamaica, some 40% <strong>of</strong> papaya orchards have been devastated by PRSV. Since genetic resistanceis not available, efforts were aimed at using transgenic resistance for the control <strong>of</strong> PRSV inJamaica. Reverse transcription <strong>and</strong> polymerase chain reaction were used to engineer coat protein(CP) gene constructs <strong>of</strong> a local PRSV isolate into plant transformation vectors. CP constructs weresubsequently introduced into Carica papaya L. embryogenic calli by microprojectile bombardmentusing NPTII <strong>and</strong> GUS as selectable markers. Some 150 transgenic lines were obtained from 18bombardment experiments. Under greenhouse conditions, R0 clones <strong>of</strong> 11 lines proved resistant torepeated manual inoculations with the virus. Similarly inoculated nontransgenic papaya plantsdeveloped symptoms 11 to 40 days after inoculation.Clones <strong>of</strong> R0 plants have since been transferred to a half-acre plot in Clarendon. Virus infectionwas first observed on nontransgenic plants 6 months after planting using natural aphid populationsas inoculum vectors. Twenty-eight transgenic lines remain symptomless <strong>and</strong> ELISA-negative.<strong>The</strong>se preliminary results suggest that transgenic resistance could be a practical solution to thePRSV problem in Jamaica.ReferencesGonsalves, D. (1994). Papaya ringspot Virus. In Compendium <strong>of</strong> Tropical Fruit Diseases. Eds RCPloetz, GA, Zentmyer, WT, Nishijima, KG <strong>and</strong> Rohrbach, HD Ohr. pp. 67-68. St Paul, MN, APSPress 88p.Yeh, S-D.<strong>and</strong> Gonsalves, D. (1994). Practices <strong>and</strong> perspectives <strong>of</strong> control <strong>of</strong> papaya ringspot virusby cross protection. In Advances in Disease Vector Research. Ed. KF Harris, 10: 237-257.New York :Springer-Verlag.O-15 GENETIC DIVERSITY AND RELATIONSHIPS AMONGGEMINIVIRUSES FROM JAMAICA AND BARBADOSMarcia E. Roye, Wayne A. McLaughlin, Medhat K. Nakhla <strong>and</strong> Douglas P. Maxwell<strong>Department</strong> <strong>of</strong> Basic Medical Sciences-Biochemistry; <strong>and</strong> <strong>The</strong> Biotechnology Centre, Mona;<strong>Department</strong> <strong>of</strong> Plant Pathology, University <strong>of</strong> Wisconsin-MadisonGeminiviral DNA probes, polymerase chain reaction <strong>and</strong> nucleotide sequencing was used to identify7 geminiviruses from Jamaica <strong>and</strong> 3 from Barbados. PCR-amplified products for DNA-A weregenerated from 80% <strong>of</strong> plants from Jamaica that gave hybridisation signals <strong>and</strong> 32% <strong>of</strong> plants fromBarbados. Nucleotide identity <strong>of</strong> the common regions <strong>of</strong> DNA-A <strong>and</strong> DNA-B, <strong>and</strong> partial nucleotidesequences <strong>of</strong> the ac1, av1, bc1, <strong>and</strong> bv1 genes confirmed the presence <strong>of</strong> bipartite geminiviruses inthe following crops from Jamaica: P. vulgaris <strong>and</strong> P. lunatus (bean golden mosaic virus, BGMV-JM2), L. esculentum <strong>and</strong> C. chinense (tomato dwarf leaf curl virus, TDLCV), <strong>and</strong> two distinctviruses infecting cabbage. <strong>The</strong> weeds associated with viruses included Sida spp. (sida golden mosaicvirus, SiGMV-JM), W. amplissima (wissadula golden mosaic virus, WGMV) <strong>and</strong> three distinctviruses in M.lathyroides (macroptilium golden mosaic virus strains 1 <strong>and</strong> 2, MacGMV-JM1,MacGMV-JM2 <strong>and</strong> SiGMV-JM).37

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