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Advances in Disease Vector Research pp 237–257Cite as

Practices and Perspective of Control of Papaya Ringspot Virus by Cross Protection

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Part of the book series: Advances in Disease Vector Research ((VECTOR,volume 10))

Abstract

Papaya (Carica papaya L.) is widely grown in tropical and subtropical areas for its edible fruit and delicate taste. The plant grows fast and the fruit can be harvested 8–10 months after transplanting the tree in the field. It continues producing fruit for 2–3 years under normal conditions. The delicious and nutritious fruit contains a popular protease, papain, which helps to digest food for assimilation. The extensive adaption of this plant and wide acceptance of the fruit offer considerable promise for papaya as a commercial crop for local and export purpose. Like banana, pineapple, and mango, papaya is one of the important cash crops in the tropics and subtropics.

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References

  1. Abel, P.P., Nelson, R.S., De, B., Hoffmann, N., Rogers, S.G., Fraley, R.T., and Beachy, R.N. 1986. Delay of disease development in transgenic plant that express the tobacco mosaic virus coat protein gene. Science 232:738–743.

    PubMed  CAS  Google Scholar 

  2. Adsuar, J. 1946. Studies on virus disease of papaya (Carica papaya) in Puerto Rico, I. Transmission of papaya mosaic. Puerto Rico Agric. Exp. Stn. Tech. Pap. 1.

    Google Scholar 

  3. Ahlquist, P., French, R., Janda, M., and Loesch-Fries, L.S. 1984. Muticomponent RNA plant virus infection derived from cloned viral cDNA. Proc. Natl. Acad. Sci. U.S.A. 81:7066–7070.

    PubMed  CAS  Google Scholar 

  4. Allison, R.F., Johnston, R.E., and Dougherty, W.G. 1986. The nucleotide sequence of the coding region of tobacco etch virus genomic RNA: Evidence for the synthesis of a single polyprotein. Virology 154:9–20.

    PubMed  CAS  Google Scholar 

  5. Arora, I.K., and Singh, R.N. 1978. Growth hormones and in vitro callus formation of papaya, Sci. Hortic. 8:357–361.

    CAS  Google Scholar 

  6. Atreya, C.D., Raccah, B., and Pirone, T.P. 1990. A point mutation in the coat protein abolishes aphid transmissibility of a potyvirus. Virology 178:161–165.

    PubMed  CAS  Google Scholar 

  7. Bevan, M. 1984. Binary Agrobacterium vectors for plant transformation. Nucl. Acids Res. 12:8711–8721.

    PubMed  CAS  Google Scholar 

  8. Bevan, M.W., Mason, S.E., and Goelet, P. 1985. Expression of tobacco mosaic virus coat protein by cauliflower mosaic virus promoter in plants transformed by Agrobacterium. EMBO J. 4:1921–1926.

    PubMed  CAS  Google Scholar 

  9. Capoor, S.P., and Varma, P.M. 1948. A mosaic disease of Carica papaya L. in the Bombay province. Current Sci. 17:265–266.

    Google Scholar 

  10. Chang, C.A. 1979. Isolation and comparison of two isolates of papaya ringspot virus in Taiwan. J. Agric. Res. China 28:207–216.

    Google Scholar 

  11. Chen, M.H., Wang, P.J., and Maeda, E. 1987. Somatic embryogenesis and plant regeneration in Carica papaya L. tissue culture derived from root explants. Plant Cell Rep. 6:348–351.

    Google Scholar 

  12. Conover, R.A. 1964. Distortion ringspot, a severe disease of papaya in Florida. Proc. Fla. State Hortic. Soc. 77:440–444.

    Google Scholar 

  13. Conover, R.A. 1976. A program for development of papayas tolerant to the distortion ringspot virus. Proc. Fla. State Hortic. Soc. 89:229–231.

    Google Scholar 

  14. Conover, R.A., and Litz, R.E. 1978. Progress in breeding papayas with tolerance to papaya ringspot virus. Proc. Fla. State Hortic. Soc. 91:182–184.

    Google Scholar 

  15. Cook, A.A. 1972. Virus diseases of papaya. Fla. Agr. Exp. Sta. Bull. 750 (Tech.), 19pp.

    Google Scholar 

  16. Cook, A.A., and Zettler, F.W. 1970. Susceptibility of papaya cultivars to papaya ringspot and papaya mosaic virus. Plant Dis. Rep. 54:893–895.

    Google Scholar 

  17. Cost, A.S., and Muller, G.W. 1980. Tristeza control by cross protection: A U.S.-Brazil cooperative success. Plant Dis. 64:538–541.

    Google Scholar 

  18. Cuozzo, M., O’cnnell, K.M., Kaniewski, W., Fang, R.X., Chua, N.H., and Turner, N. 1988. Viral protection in transgenic tobacco plants expressing the cucumber mosaic virus coat protein or its antisense RNA. Biotechnology 6:549–557.

    CAS  Google Scholar 

  19. Dawson, W.O., Beck, D.L., Knorr, D.A., and Grantham, G.L. 1986. cDNA cloning of the complete genome of tobacco mosaic virus and production of infectious transcript. Proc. Natl. Acad. Sci. U.S.A. 83:1832–1836.

    PubMed  CAS  Google Scholar 

  20. De La Rosa, M., and Lastra, R. 1983. Purification and partial characterization of papaya ringspot virus. Phytopathol. Z. 106:329–336.

    Google Scholar 

  21. De Mejia, M.V.G., Hiebert, E., and Purcifull, D.E. 1985. Isolation and partial characterization of the amorphous cytoplasmic inclusions associated with infections caused by two potyviruses. Virology 142:24–33.

    PubMed  Google Scholar 

  22. De Mejia, M.V.G., Hiebert, E., Purcifull, D.E., Thornbury, D.W., and Pirone, T.P. 1985. Identification of potyviral amorphous inclusion protein as a nonstructural, virus-specific protein related to helper component. Virology 142:34–43.

    PubMed  Google Scholar 

  23. De Zoeten, G.A., and Fulton, R.W. 1975. Understanding generates possibilities. Phytopathology 65:221–222.

    Google Scholar 

  24. Domier, L.L., Franklin, K.M., Shahabuddin, M., Hellmann, G.M., Lomonossoff, G.P., Shaw, J.G., and Rhoads, R.D. 1986. The nucleotide sequence of tobacco vein mottling virus RNA. Nucl. Acids Res. 13:5417–5430.

    Google Scholar 

  25. Domier, L.L., Franklin, K.M., Hunt, A.G., Rhoads, R.E., and Shaw, J.G. 1989. Infectious in vitro transcript from cloned cDNA of a potyvirus, tobacco vein mottling virus. Proc. Natl. Acad. Sci. U.S.A. 86:3509–3513.

    PubMed  CAS  Google Scholar 

  26. Fitch, M.M.M., and Manshardt, R.M. 1990. Somatic embryogenesis and plant regeneration from immature zygotic embryos of papaya (Carica papaya L.). Plant Cell Rep. 9:320–324.

    CAS  Google Scholar 

  27. Fitch, M.M.M., Manshardt, R.M., Gonsalves, D., Slightom, J.L., and Sanford, J.C. 1990. Stable transformation of papaya via microprojectile bombardment. Plant Cell Rep. 9:189–194.

    CAS  Google Scholar 

  28. Fitch, M.M.M., Manshardt, R.M., Gonsalves, D., Slightom, J.L., and Sanford, J.C. 1992. Virus resistant papaya plants derived from tissues bombarded with the coat protein gene of papaya ringspot virus. Bio/ Technology 10:1466–1472.

    CAS  Google Scholar 

  29. Fletcher, J.T. 1978. The use of avirulent virus strains to protect plants against the effects of virulent strains. Ann. Appl. Biol. 89:110–114.

    Google Scholar 

  30. Fletcher, J.T., and Rowe, J.M. 1975. Observations and experiments on the use of an avirulent mutant strain of tobacco mosaic virus as a means of controlling tomato mosaic. Ann. Appl. Biol. 81:171–179.

    PubMed  CAS  Google Scholar 

  31. Frazer, L.R., Long, K., and Cox, J. 1968. Stem pitting of grapefruit-field protection by the use of mild virus strains. Proceeding, 4th Conference of the International Organization of Citrus Virologists, pp. 27–31.

    Google Scholar 

  32. French, R., and Ahlquist, P. 1988. Characterization and engineering of sequences controlling in vivo synthesis of brome mosaic virus subgenomic RNA. J. Virol. 52:2411–2420.

    Google Scholar 

  33. Fulton, R.W. 1986. Practices and precautions in the use of cross protection for plant virus disease control. Annu. Rev. Phytopathol. 24:67–81.

    Google Scholar 

  34. Gal-On, A., Antignus, Y., Rosner, A., and Raccah, B. 1991. Infectious in vitro RNA transcripts derived form cloned cDNA of the cucurbit potyvirus, zucchini yellow mosaic virus. J. Gen. Virol. 72:2639–2643.

    PubMed  CAS  Google Scholar 

  35. Gibbs, A. 1969. Plant virus classification. Adv. Virus Res. 14:263–328.

    PubMed  CAS  Google Scholar 

  36. Gierer, A., and Mundry, K.W. 1958. Production of mutants of tobacco mosaic virus by chemical alteration of its ribonucleic acid. Nature (London) 182:1457–1458.

    CAS  Google Scholar 

  37. Gonsalves, D., and Garnsey, S.M. 1989. Cross protection techniques for control of virus diseases in the tropics. Plant Dis. 73:592–597.

    Google Scholar 

  38. Gonsalves, D., and Ishii, M. 1980. Purification and serology of papaya ringspot virus. Phytopathology 70:1028–1032.

    CAS  Google Scholar 

  39. Grant, T.J., and Costa, A.S. 1951. A mild strain of the tristeza virus of citrus. Phytopathology 41:114–122.

    Google Scholar 

  40. Grant, T.J., and Higgins, R.P. 1957. Occurrence of mixture of tristeza virus strains in citrus. Phytopathology 47:272–276.

    Google Scholar 

  41. Heaton, L.A., Carrington, J.C., and Morris, T.J. 1989. Turnip crinkle virus infection from RNA synthesized in vitro. Virology 170:214–218.

    PubMed  CAS  Google Scholar 

  42. Hemenway, C., Fang, R.X., Kaniewski, W., Chua, N.H., and Tumer, N.E. 1988. Analysis of the mechanism of protection in transgenic plants expressing potato virus X protein or its antisense RNA. EMBO J. 7:1273–1280.

    PubMed  CAS  Google Scholar 

  43. Herold, F., and Weibel, J. 1962. Electron microscopic demonstration of papaya ringspot virus. Virology 18:307–311.

    Google Scholar 

  44. Hoekema, A., Hirsch, P.R., Hooykaas, P.J.J., and Schilperoort, R.A. 1983. A binary plant vector strategy based on separation of Vir and T-region of the Agrobacterium tumefaciens Ti-plasmid. Nature (London) 303:179–180.

    CAS  Google Scholar 

  45. Holt, C.A., Hodgson, R.A., Coker, F.A., Beachy, R.N., and Nelson, R.S. 1990. Characterization of the masked strain of tobacco mosaic virus: Identification of the region responsible for symptom attenuation by analysis of an infectious cDNA clone. Mol. Plant-Microbe Interact. 3:417–423.

    PubMed  CAS  Google Scholar 

  46. Jensen, D.D. 1949. Papaya ringspot virus and its insect vector relationships. Phytopathology 39:212–220.

    Google Scholar 

  47. Johansen, E., Rasmussen, O.F., Heide, M., and Borkhardt, B. 1991. The complete nucleotide sequence of pea seed-borne mosaic virus RNA. J. Gen. Virol. 72:2625–2632.

    PubMed  CAS  Google Scholar 

  48. Khuspe, S.S., Hendre, R.R., Mascarenhas, A.F., Jagannathan, V., Thombre, M.V., and Joshi, A.B. 1980. Utilization of tissue culture to isolate interspecific hybrids in Carica L. In P.S. Rao, M.R. Heble, and M.S. Chadha, eds., Plant Tissue Culture, Genetic Manipulation and Somatic Hybridization of Plant Cells. Bhabha Atomic Research Center, Bombay, India, pp. 198–205.

    Google Scholar 

  49. Lana, A.F. 1980. Transmission and properties of virus isolated from Carica papaya in Nigeria. J. Hortic. Sci. 55:191–197.

    Google Scholar 

  50. Lawson, C., Kaniewski, W., Haley, L., Rozman, R., Newell, C., Sanders, P., and Tumer, N.E. 1990. Engineering resistance to mixed virus infection in a commercial potato cultivar: resistance to potato virus X and potato virus Y in transgenic russet burbank. Biotechnology 8:127–134.

    PubMed  CAS  Google Scholar 

  51. Lin, C.C. 1980. Strains of papaya ringspot virus and their cross protection. Ph.D. thesis, National Taiwan University, Taipei.

    Google Scholar 

  52. Linder, R.C., Jensen, D.D., and Ikeda, W. 1945. Ringspot: new papaya plunderer. Hawaii Farm Home 8:10–14.

    Google Scholar 

  53. Ling, K., Namba, S., Gonsalves, C., Slightom, J.L., and Gonsalves, D. 1991. Protection against detrimental effects of potyvirus infection in transgenic tobacco plants expressing the papaya ringspot virus coat protein gene. Biotechnology 9:752–748.

    PubMed  CAS  Google Scholar 

  54. Litz, R.E. 1984. Papaya. In D.A. Evans, W.R. Sharp, P.V. Ammirato, and Y. Yanada, eds., Handbook of Plant Cell Culture, Vol. 2. New York, Macmillan, pp. 349–368.

    Google Scholar 

  55. Litz, R.E., and Conover, R.A. 1981. Effect of sex type, season, and other factors on in vitro establishment and culture of Carica papaya L. expiants. J. Am. Soc. Hortic. Sci. 106:792–794.

    Google Scholar 

  56. Litz, R.E., and Conover, R.A. 1982. In vitro somatic embryogenesis and plant regeneration from Carica papaya L. ovular callus. Plant Sci. Lett. 26:153–158.

    CAS  Google Scholar 

  57. Litz, R.E., and Conover, R.A. 1983. High-frequency somatic embryogenesis from Carica suspension culture. Ann Bot. 51:683–686.

    Google Scholar 

  58. Litz, R.E., O’Hair, S.K., and Conover, R.A. 1983. In vitro growth of Carica papaya L. cotyledons. Sci. Hort. 19:287–293.

    CAS  Google Scholar 

  59. Loesch-Fries, L.S., Merlo, D., Zinnen, T., Burhop, L., Hill, K., Krahn, K., Jarvis, N., Nelson, S., and Halk, E. 1987. Expression of alfalfa mosaic virus RNA 4 in transgenic plants confers virus resistance. EMBO J. 6:1845–1851.

    PubMed  CAS  Google Scholar 

  60. Maiss, E., Timpe, U., Brisske, A., Jelkmann, W., Casper, R., Himmler, G., Mattanovich, D., and Katinger, H.W.D. 1989. The complete nucleotide sequence of plum pox virus RNA. J. Gen. Virol. 70:513–524.

    PubMed  CAS  Google Scholar 

  61. Manshardt, R.M., and Wenslaff, T.F. 1989. Zygotic polyembryony in interspecific hybrids of Carica papaya and C. cauliflora. J. Am Soc. Hort. Sci. 114:684–689.

    Google Scholar 

  62. Manshardt, R.M., and Wenslaff, T.F. 1989. Interspecific hybridization of papaya with other Carica species. J. Am. Soc. Hort. Sci. 114:689–694.

    Google Scholar 

  63. Martelli, G.P., and Russo, M. 1976. Unusual cytoplasmic inclusions induced by watermelon mosaic virus. Virology 72:352–362.

    PubMed  CAS  Google Scholar 

  64. Mau, R.F.L., Gonsalves, D., and Bautista, R. 1990. Use of cross-protection to control papaya ringspot virus at Waianae. Proc. 25th Annual Papaya Industry Association Conference, 1989, pp. 77–84.

    Google Scholar 

  65. McKinney, H.H. 1929. Mosaic diseases in the Canary Islands, West Africa, and Gibraltar. J. Agric. Res. 39:557–578.

    Google Scholar 

  66. McMillan, Jr., R.T., and Gonsalves, D. 1987. Effectiveness of cross-protection by a mild mutant of papaya ringspot virus for control of ringspot disease of papaya in Florida. Proc. Fla. State Hort. Soc. 100:294–296.

    Google Scholar 

  67. Mekako, H.U., and Nakasone, H.Y. 1975. Interspecific hybridization among six Carica species. J. Am. Soc. Hortic. Sci. 100:237–242.

    Google Scholar 

  68. Meshi, T., Ishikawa, M., Motoyoshi, F., Semba, K., and Okada, Y. 1986. In vitro transcription of infectious RNAs from full-length cDNAs of tobacco mosaic virus. Proc. Natl. Acad. Sci. U.S.A. 83:5043–5047.

    PubMed  CAS  Google Scholar 

  69. Muller, G.W., and Costa, A.S. 1977. Tristeza control in Brazil by preimmunization with mild strains. Proc. Int. Soc. Citric. 3:868–872.

    Google Scholar 

  70. Mundry, K.W. 1959. The effect of nitrous acid on tobacco mosaic virus: Mutation not selection. Virology 9:722–726.

    PubMed  CAS  Google Scholar 

  71. Nagel, J., and Hiebert, E. 1985. Complementary DNA cloning and expressing of the papaya ringspot potyvirus sequences encoding capsid protein and a nuclear inclusion-like protein in Escherichia coli. Virology 143:435–441.

    PubMed  CAS  Google Scholar 

  72. Namba, R., and Higa, S.Y. 1977. Retention of the inoculativity of the papaya mosaic virus by the green peach aphid. Proc. Hawaii Entomol. Soc. 22:491–494.

    Google Scholar 

  73. Nelson, R.S., McCormick, S.M., Delannay, X., Dube, P., Layton, J., Anderson, E.J., Kaniewska, M., Proksch, R.K., Horsch, R.B., Rogers, S.G., Fraley, R.T., and Beachy, R.N. 1988. Virus tolerance, plant growth, and field performance of transgenic tomato plants expressing coat protein from tobacco mosaic virus. Biotechnology 6:403–409.

    Google Scholar 

  74. Olson, E.O. 1956. Mild and severe strains of the tristeza virus in Texas citrus. Phytopathology 46:336–341.

    Google Scholar 

  75. Olson, E.O. 1958. Responses of lime and sour orange seedlings and four scion rootstock combinations to infection by strains of the tristeza virus. Phytopathology 48:454–459.

    Google Scholar 

  76. Oshima, N. 1975. The control of tomato mosaic disease with attenuated virus of tomato strain of TMV. Rev. Plant Prot. Res. 8:126–135.

    Google Scholar 

  77. Pang, S.Z., and Sanford, J.C. 1988. Agrobacterium-mediated gene transfer in papaya. J. Am. Soc. Hort. Sci. 113:287–291.

    CAS  Google Scholar 

  78. Ponz, F., and Bruening, G. 1986. Mechanism of resistance to plant viruses. Annu. Rev. Phytopathol. 24:355–381.

    CAS  Google Scholar 

  79. Price, W.C. 1970. Citrus tristeza virus. CMI/AAB Description of Plant Viruses, No. 33.

    Google Scholar 

  80. Provvidenti, R., and Gonsalves, D. 1982. Resistance to papaya ringspot virus in Cucumis metuliferus and its relationship to watermelon mosaic virus 1. J. Hered. 73:239–240.

    Google Scholar 

  81. Purcifull, D.E., and Edwardson, J.R. 1967. Watermelon mosaic virus: tubular inclusion in pumpkin leaves and aggregates in leaf extracts. Virology 32:393–401.

    PubMed  CAS  Google Scholar 

  82. Purcifull, D.E., and Hiebert, E. 1979. Serological distinction of watermelon mosaic virus isolates. Phytopathology 69:112–116.

    Google Scholar 

  83. Purcifull, D.E., Edwardson, J., Hiebert, E., and Gonsalves, D. 1984. Papaya ringspot virus. CMI/AAB Descriptions of Plant Viruses, No. 292.

    Google Scholar 

  84. Quemada, H., L’Hostis, B., Gonsalves, D., Reardon, I.M., Heinrikson, R., Hiebert, E.L., Sieu, L.C., and Slightom, J.L. 1990. The nucleotide sequences of the 3′-terminal regions of papaya ringspot virus strains W and P. J. Gen. Virol. 71:203–210.

    PubMed  CAS  Google Scholar 

  85. Quiot-Douine, L., Purcifull, D.E., and de Mejia, M.V.G. 1986. Serological relationships and in vitro translation of an antigenically distinct strain of papaya ringspot virus. Phytopathology 76:346–351.

    Google Scholar 

  86. Rast, A.T.B. 1972. M II-16, an artificial symptomless mutant of tobacco mosaic for seedling inoculation of tomato crops. Neth. J. Plant Pathol. 78:110–112.

    Google Scholar 

  87. Rast, A.T.B. 1975. Variability of tobacco mosaic virus in relation to control tomato mosaic in greenhouse tomato crops by resistance breeding and cross protection. Agr. Res. Rept. 834:1–76. Inst. Phytopathol. Res. Wageningen, The Netherlands.

    Google Scholar 

  88. Riechmann, J.L., Lain, S., and Garcia, J.A. 1990. Infectious in vitro transcripts from plum pox potyvirus cDNA clone. Virology 177:710–716.

    PubMed  CAS  Google Scholar 

  89. Robaglia, C., Durand-Tardif, M., Tronchet, M., Boudazin, G., Astier-Manifacier, S., and Casse-Delbart, F. 1989. Nucleotide sequence of potato virus Y (N strain) genomic RNA. J. Gen. Virol. 70:935–947.

    PubMed  CAS  Google Scholar 

  90. Siegel, A. 1965. Artificial production of mutants of tobacco mosaic virus. Adv. Virus Res. 11:25–60.

    PubMed  CAS  Google Scholar 

  91. Singh, A.B. 1969. A new virus disease of Carica papaya in India. Plant Dis. Rep. 53:267–269.

    Google Scholar 

  92. Story, G.E., and Halliwell, R.S. 1969. Identification of distortion ringspot virus disease of papaya in the Dominican Republic. Plant Dis. Rep. 53:757–760.

    Google Scholar 

  93. Stubbs, L.L. 1964. Transmission and protective inoculation studies with viruses of the citrus tristeza complex. Aust. J. Agr. Res. 15:752–770.

    Google Scholar 

  94. Turner, N.E., O’Connell, K.M., Nelson, R.S., Sanders, P.R., Beachy, R.N., Fraley, R.T., and Shah, D.M. 1987. Expression of alfalfa mosaic virus coat protein gene confers cross-protection in transgenic tobacco and tomato plants. EMBO J. 6:1181–1188.

    Google Scholar 

  95. van der Werf, S., Bradley, J., Wimmer, E., Studier, F.W., and Dunn, J.J. 1986. Synthesis of infectious polio virus RNA by purified T7 RNA polymerase. Proc. Natl. Acad. Sci. U.S.A. 83:2330–2334.

    PubMed  Google Scholar 

  96. van Dun, C.M.P., Bol, J.F., and van Vloten-Doting, L. 1987. Expression of alfalfa mosaic virus and tobacco rattle virus protein genes in transgenic tobacco plants. Virology 159:299–305.

    PubMed  Google Scholar 

  97. van Dun, C.M.P., Overduin, B., van Vloten-Doting, L., and Bol, J.F. 1988. Transgenic tobacco streak virus or mutated alfalfa mosaic virus coat protein does not cross-protect against alfalfa mosaic virus infection. Virology 164:383–389.

    PubMed  Google Scholar 

  98. Verchot, J., Koonin, E.V., and Carrington, J.C. 1991. The 35-kDa protein from the N-terminus of the potyviral polyprotein functions as a third virus-encoded proteinase. Virology 185:527–535.

    PubMed  CAS  Google Scholar 

  99. Vos, P., Jaegle, M., Wellink, J., Verver, J., Eggen, R., van Kammen, A., and Goldbach, R. 1988. Infectious RNA transcripts derived from full-length DNA copies of the genomic RNAs of cowpea mosaic virus. Virology 165:33–41.

    PubMed  CAS  Google Scholar 

  100. Wang, C.H., and Yeh, S.-D. 1992. Nucleotide sequence comparison of the 3’terminal region of severe, mild, and non-papaya infecting strains of papaya ringspot virus. Arch. Virol. 127:345–354.

    PubMed  CAS  Google Scholar 

  101. Wang, H.L., Wang, C.C., Chiu, R.J., and Sun, M.H. 1978. Preliminary study on papaya ringspot virus in Taiwan. Plant Prot. Bull. (Taiwan) 20:133–140.

    Google Scholar 

  102. Wang, H.L., Yeh, S.-D., Chiu, R.-J., and Gonsalves, D. 1987. Effectiveness of cross-protection by mild mutants of papaya ringspot virus for control of ringspot disease of papaya in Taiwan. Plant Dis. 71:491–497.

    Google Scholar 

  103. Yamaya, J., Yoshioka, M., Meshi, T., Okada, Y., and Ohno, T. 1988. Expression of tobacco mosaic virus RNA in transgenic plants. Mol. Gen. Genet. 211:520–525.

    PubMed  CAS  Google Scholar 

  104. Yeh, S.-D., and Gonsalves, D. 1984. Evaluation of induced mutants of papaya ringspot virus for control by cross protection. Phytopathology 74:1086–1091.

    Google Scholar 

  105. Yeh, S.-D., and Gonsalves, D. 1984. Purification and immunological analyses of cylindrical-inclusion protein induced by papaya ringspot virus and watermelon mosaic virus 1. Phytopathology 74:1273–1278.

    CAS  Google Scholar 

  106. Yeh, S.-D., and Gonsalves, D. 1985. Translation of papaya ringspot virus RNA in vitro: Detection of a possible polyprotein that is processed for capsid protein, cylindrical-inclusion protein, and amorphous-inclusion protein. Virology 143:260–271.

    PubMed  CAS  Google Scholar 

  107. Yeh, S.-D., and Bih, F.Y. 1989. Comparative studies on in vitro translation of a severe strain and a mild strain of papaya ringspot virus. Plant Prot. Bull. (Taiwan, R.O.C.) 31:276–289.

    CAS  Google Scholar 

  108. Yeh, S.-D., and Cheng, Y.-H. 1989. Use of resistant Cucumis metuliferus for selection of nitrous-acid induced attenuated strains of papaya ringspot virus. Phytopathology 79:1257–1261.

    Google Scholar 

  109. Yeh, S.-D., Gonsalves, D., and Provvidenti, R. 1984. Comparative studies on host range and serology of papaya ringspot virus and watermelon mosaic virus 1. Phytopathology 74:1081–1085.

    Google Scholar 

  110. Yeh, S.-D., Gonsalves, D., Wang, H.-W., Namba, R., and Chiu, R.-J. 1988. Control of papaya ringspot virus by cross protection. Plant Dis. 72:375–380.

    Google Scholar 

  111. Yeh, S.-D., Jan, F.-J., Chiang, C.-H., Doong, T.-J., Chen, M.-C., Chung, P.-H., and Bau, H.-J. 1992. Complete nucleotide sequence and genetic organization of papaya ringspot virus RNA. J. Gen. Virol. 73:2531–2541.

    PubMed  CAS  Google Scholar 

  112. Yie, S.T., and Liaw, S.I. 1977. Plant regeneration from shoot tips and callus of papaya. In Vitro 13:564–567.

    PubMed  CAS  Google Scholar 

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Authors and Affiliations

  1. Department of Plant Pathology, National Chung Hsing University, Taichung, Taiwan, Republic of China

    Shyi-Dong Yeh

  2. Department of Plant Pathology, New York State Agricultural Experiment Station, Cornell University, Geneva, New York, 14456, USA

    Dennis Gonsalves

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  1. Virus-Vector Research Laboratory, Department of Entomology, Texas A&M University College Station, Texas, 77843, USA

    Kerry F. Harris

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Yeh, SD., Gonsalves, D. (1994). Practices and Perspective of Control of Papaya Ringspot Virus by Cross Protection. In: Harris, K.F. (eds) Advances in Disease Vector Research. Advances in Disease Vector Research, vol 10. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-2590-4_9

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  • DOI: https://doi.org/10.1007/978-1-4612-2590-4_9

  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4612-7596-1

  • Online ISBN: 978-1-4612-2590-4

  • eBook Packages: Springer Book Archive

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