Breeding for disease resistance of Penaeid shrimps

Aquaculture

Volumn 286, Issue 1-2, 2009, Pages 1-11

  Cock, James ^a   Gitterle, Thomas ^a   Salazar, Marcela ^a   Rye, Morten ^b  

^a CENIACUA   (Colombia)

^b NOFIMA   (Norway)

Author keywords

Breeding; Disease resistance; Penaeid shrimps; Selection

Indexed keywords

CRUSTACEAN; DISEASE CONTROL; DISEASE RESISTANCE; GENETIC VARIATION; RECOMBINATION; SELECTIVE BREEDING; VIRAL DISEASE; VIRUS;

ANIMALIA; CRUSTACEA; DECAPODA (CRUSTACEA); PENAEIDAE; SHRIMP WHITE SPOT SYNDROME VIRUS; TAURA SYNDROME VIRUS;

EID: 56949084980     PISSN: 00448486     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.aquaculture.2008.09.011     Document Type: Review

References (96)

1. Anon. White Spot Disease, Brazil (2005). http://www.aphis.usda.gov/vs/ceah/cei/IW_2005_files/WhiteSpot_Brazil_012 705_files/WhitespotdiseaseBrazil012105.htm http://www.aphis.usda.gov/vs/ceah/cei/IW_2005_files/WhiteSpot_Brazil_012 705_files/WhitespotdiseaseBrazil012105.htm
2. Aparicio J.P., Solari H.G., and Bonino N. Competition and coexistence in host-parasite systems: the myxomatosis case. Popul. Ecol. 46 (2004) 71-85
3. Argue B.J., Arce S.M., Lotz J.M., and Moss S.M. Selective breeding of Pacific white shrimp (Litopenaeus vannamei) for growth and resistance to Taura Syndrome Virus. Aquaculture 204 (2002) 447-460
4. Biggs P.M. Infectious animal disease and its control. Phil. Trans. R. Soc. London. B. 310 (1985) 259-274
5. Bishop S., Chesnais J., and Stear M.J. Breeding for disease resistance: issues and opportunities. Proc. 7th World Congress on Genetics Applied to Livestock Production (2002), Montpellier, Communication 13-01 597-604
6. Brock J.A. Taura syndrome, a disease important to shrimp farms in the Americas. J. World Aquac. Soc. 13 (1997) 415-418
7. Brown J.K.M. A cost of disease resistance: paradigm or peculiarity?. Trends Genet. 19 (2003) 667-671
8. Carius H.J., Little T.J., and Ebert D. Genetic variation in a host-parasite association: potential for coevolution and frequency-dependent selection. Evolution 55 (2001) 1136-1145
9. Chou H.Y., Huang C.Y., Wang C.H., Chiang H.C., and Lo C.F. Pathogenicity of a baculovirus infection causing white spot syndrome in cultured penaeid shrimp in Taiwan. Dis. Aquat. Org. 23 (1995) 165-173
10. Coustau C., Chevillon C., and Ffrench-Constant R. Resistance to xenobiotics and parasites: can we count the cost?. Tree 15 (2000) 378-383
11. Davis W. One River: Explorations and Discoveries in the Amazon Rain Forest (1996), Touchstone, New York, USA
12. De Donato M., Manrique R., Ramirez R., Mayer L., and Howell C. Mass selection and inbreeding effects on a cultivated strain of Penaeus (Litopenaeus) vannamei in Venezuela. Aquaculture 247 (2005) 159-167
13. Detilleux J. Genetic improvement of resistance to infectious diseases in livestock. J. Dairy Sci. 84 (2001) 39-46
14. Doyle R.W., Moss D.R., and Moss S.M. Shrimp copyright: inbreeding strategies effective against illegal copying of genetically improved shrimp. Global Aquac. Advocate (2006) 76-79 (April/May)
15. Drake J.W. A constant rate of spontaneous mutation in DNA-based microbes. Proc. Natl. Acad. Sci. U. S. A. 88 (1991) 7160-7164
16. Dudley J.W., and Lambert R.J. 100 generations of selection for oil and protein in corn. Plant Breed. Rev. 24 (2004) 79-85
17. Ebert D. Experimental evolution of parasites. Science 282 (1998) 1432-1435
18. Fjalestad K.T. In: Gjedrem T. (Ed). Selection Methods. In Selection and Breeding Programs in Aquaculture (2005), Springer, Netherlands 159-171
19. Fjalestad K.T., Gjedrem T., and Gjerde B. Genetic improvement of disease resistance in fish: an overview. Aquaculture 111 (1993) 65-74
20. Fjalestad K.T., Gjedrem T., Carr W.H., and Sweeney J.N. Final Report: The Shrimp Breeding Program, Selective Breeding of Penaeus vannamei (1997), The Oceanic Institute, Waimanalo, HI, USA
21. Flegel T.W., and Alday-Sanz V. The crisis in Asian shrimp aquaculture: current status and future needs. J. Appl. Ichthyol. 14 (1998) 269-273
22. Flegel T.W., Nielsen L., Thamavit V., Kongtim S., and Pasharawipas T. Presence of multiple viruses in non-diseased, cultivated shrimp at harvest. Aquaculture 240 (2004) 55-68
23. Foster P.L. Adaptive mutation in Escherichia coli. J. Bacteriol. 186 15 (2004) 4846-4852
24. Frankham R., Ballou J.D., and Briscoe D.A. Introduction to Conservation Genetics (2002), Cambridge University Press, UK 617 pp.
25. Galvani A.P., and Slatkin M. Evaluating plague and smallpox as historical selective pressures for the CCR5-delta 32 HIV-resistance allele. Proc. Natl. Acad. Sci. U. S. A. 100 (2003) 15276-15279
26. Gemmill A.W., and Read A.F. Counting the cost of disease resistance. Trends Ecol. Evol. 13 (1998) 8-9
27. Gitterle, T., 1999. Evaluación de la resistencia de diferentes poblaciones del camarón marino Litopenaeus vannamei (Boone 1931) al Virus del Síndrome del Taura (TSV) bajo condiciones controladas. Thesis. Universidad Jorge Tadeo Lozano, Bogota, Colombia, 74 pp.
28. Gitterle T., Salte R., Gjerde B., Cock J., Johansen H., Salazar M., Lozano C., and Rye M. Genetic (co)variation in resistance to white spot syndrome virus (WSSV) and harvest weight in Penaeus (Litopenaeus) vannamei. Aquaculture 246 (2005) 139-149
29. Gitterle T., Ødegård J., Gjerde B., Rye M., and Salte R. Genetic parameters and accuracy of selection for resistance to White Spot Syndrome Virus (WSSV) in Penaeus (Litopenaeus) vannamei using different statistical models. Aquaculture 251 (2006) 210-218
30. Goyard E., Patrois J., Peignon J., Vanaa V., Dufour R., Viallon J., and Bedier E. Selection for better growth of Penaeus stylirostris in Tahiti and New Caledonia. Aquaculture 204 (2002) 461-468
31. Harshman L.G., and Hoffmann A.A. Laboratory selection experiments using Drosophila: what do they really tell us?. Tree 15 (2000) 32-36
32. Heil M., and Baldwin I.T. Fitness costs of induced resistance: emerging experimental support for a slippery concept. Trends Plant Sci. 7 (2002) 61-67
33. Hennig O.L., Arce S.M., Moss S.M., Pantoja C.R., and Lightner D.V. Development of a specific pathogen free population of the Chinese fleshy prawn, Fenneropenaeus chinensis Part II. Second. Quar. Aquac. 250 (2005) 579-585
34. Hill A.V.S. The genomics and genetics of human infectious disease susceptibility. Annu. Rev. Genom. Hum. Genet. 2 (2001) 373-400
35. Hill W.G., and Bunger L. Inferences on the genetics of quantitative traits from long-term selection in laboratory and domestic animals. Plant Breed. Rev. 24 (2004) 169-210
36. Holtsmark M., Sonesson A.K., Gjerde B., and Klemetsdal G. Number of contributing subpopulations and mating design in the base population when establishing a selective breeding program for fish. Aquaculture 258 (2006) 241-249
37. Huang C.M., and Liao I.C. Response to mass selection for growth rate in Oreochromis niloticus. Aquaculture 85 (1990) 199-205
38. Hulbert S.C., Webb C.A., Smith S.M., and Qing S. Resistance gene complexes: evolution and utilization. Annu. Rev. Phytopathol. 39 (2001) 285-312
39. Hurst L.D., and Smith N.G.C. Do essential genes evolve slowly?. Curr. Biol. 9 (1999) 747-750
40. Imhof M., and Schlotterer C. Fitness effects of advantageous mutations in evolving Escherichia coli populations. Proc. Natl. Acad. Sci. U. S. A. 98 (2001) 1113-1117
41. Inouye K., Tamaki M., Miwa S., Oseko N., Nakano H., Kimura T., Momoyama K., and Hiraoka M. Mass mortality of cultured kuruma shrimp Penaeus japonicus in Japan in 1993: electron microscopic evidence of the causative virus. Fish Pathol. 29 (1994) 149-158
42. Jennings P.R., and Cock J.H. Centres of origin of crops and their productivity. Econ. Bot. 31 (1977) 51-54
43. Jory D.E., and Dixon H.M. Shrimp white spot syndrome virus in the western hemisphere. Aquac. Mag. 25 (1999) 83-91
44. Kawano K., and Cock J.H. Breeding cassava for underprivileged: institutional, socio-economic and biological factors for success. J. Crop. Improv. 14 (2005) 197-219
45. Keen N., Staskawicz B., Mekalanos J., Ausubel F., and Cook R.J. Introduction. In: Keen N.T. (Ed). (NAS Colloquium) Virulence and defense in host-pathogen interactions: Common features between plants and animals (2001), National Academies Press, Washington, DC, USA vi-vii
46. Kraaijeveld A.R., and Godfray H.C.J. Trade-off between parasitoid resistance and larval competitive ability in Drosophila melanogaster. Nature 389 (1997) 278-280
47. Leach J.E. Pathogen fitness penalty as a predictor of durability of disease resistance genes. Annu. Rev. Phytopathol. 39 (2001) 187-224
48. Lightner D.V. Epizootiology, distribution and the impact on international trade of two penaeid shrimp viruses in the Americas. Rev. Sci. Tech. 15 (1996) 579-601
49. Lightner D.V. The penaeid shrimp viruses TSV, IHHNV, WSSV, and YHV: current status in the Americas, available diagnostic methods and management strategies. J. Appl. Aquac. 9 (1999) 27-52
50. Lightner D.V. Biosecurity in shrimp farming: pathogen exclusion through use of SPF stock and routine surveillance. J. World Aquac. Soc. 36 (2005) 229-248
51. Lightner D.V. The penaeid shrimp viral pandemics due to IHHNV, WSSV, TSV and YHV: History in the Americas and current status. In: Walker P.J., Lester R.G., and Bondad-Reantaso M.G. (Eds). Diseases in Asian Aquaculture. Crustacean Pathology and Diseases (2005), Fish Health Section, Asian Fisheries Society, Manila 1-20
52. Lo C.F., Ho C.H., Peng S.E., Chen C.H., Hsu H.C., Chiu Y.L., Chang C.F., Liu K.F., Su M.S., Wang C.H., and Kou G.H. White spot syndrome baculovirus (WSBV) detected in cultured and captured shrimp, crabs and other arthropods. Dis. Aquat. Org. 27 (1996) 215-226
53. Mazel D., and Davies J. Antibiotic resistance in microbes. Cell. Mol. Life Sci. 56 (1999) 742-754
54. McCallum H.I., Kurisb A., Harvell C.D., Lafferty K.D., Smith G.W., and Porter J. Does terrestrial epidemiology apply to marine systems?. Trends Ecol. Evol. 19 (2004) 585-591
55. McIntosh R.P. Changing paradigms in shrimp farming: 1. General description. Global Aquac. Advocate 2 (1999) 40-47
56. Milne C.P.J. Honey bee (Hymenotpera: Apidae) hygienic behavior and resistance to chalkbrood. Ann. Entomol. Soc. Am. 76 (1983) 384-387
57. Miles J.W., and Pandey S. Long-term selection in plants in the developing world. Plant Breed. Rev. 24 (2004) 45-58
58. Moss S.M. Biosecure shrimp production: emerging technologies for a maturing industry. Global Aquac. Advocate 2 (1999) 50-52
59. Moss S.M., Arce S.M., Moss D.R., and Otoshi C.A. Disease prevention strategies for penaeid shrimp culture. Proceedings of the 32nd US Japan Symposium on Aquaculture (2003)
60. Moss S.M., Doyle R.W., and Lightner D.V. Breeding shrimp for disease resistance: challenges and opportunities for improvement. In: Walker P.J., Lester R.G., and Bondad-Reantaso M.G. (Eds). Diseases in Asian Aquaculture V (2005), Fish Health Section, Asian Fisheries Society, Manila 379-395. http://www.fhs-afs.org/daa_v_files/Chapter6_Diseases_Crustaceans/Breedin g%20Shrimp%20for%20Disease%20Resistance.pdf http://www.fhs-afs.org/daa_v_files/Chapter6_Diseases_Crustaceans/Breedin g%20Shrimp%20for%20Disease%20Resistance.pdf
61. Moss D.R., Moss S.M., and Doyle R.W. Effects of inbreeding on survival and growth of the Pacific White Shrimp, Litopenaeus vannamei. Aquaculture 272 (2007) S30-S37
62. Nell J.A., and Hand R.E. Evaluation of the progeny of second-generation Sydney rock oyster Saccostrea glomerata (Gould, 1850) breeding lines for resistance to QX disease Marteilia Sydney. Aquaculture 228 (2003) 27-35
63. NOAH. Vaccination of farm animals. Briefing Document No. 22 National Office of Animal Health (2002), Middlesex, UK. http://www.noah.co.uk/issues/briefingdoc/bd22.pdf http://www.noah.co.uk/issues/briefingdoc/bd22.pdf
64. Nunan L.M., Pantoja C.R., Salazar M., Aranguren L.F., and Lightner D.V. Characterization and molecular methods for detection of a novel spiroplasma pathogenic to Penaeus vannamei. Dis. Aquat. Org. 62 (2004) 255-264
65. O'Brien S.J., and Moore J.P. The effect of genetic variation in chemokines and their receptors on HIV transmission and progression to AIDS. Immunol. Rev. 177 (2000) 99-111
66. Ødegård J., Olesen I., Gjerde B., and Klemetsdal G. Evaluation of statistical models for genetic analysis of challenge test data on furunculosis resistance in Atlantic salmon (Salmo salar): prediction of field survival. Aquaculture 259 (2006) 116-123
67. Ødegård J., Olesen I., Gjerde B., and Klemetsdal G. Evaluation of statistical models for genetic analysis of challenge-test data on ISA resistance in Atlantic salmon (Salmo salar): prediction of progeny survival. Aquaculture 266 (2007) 70-76
68. Orr H.A. The population genetics of adaptation: the distribution of factors fixed during adaptive evolution. Evolution 52 (1998) 935-949
69. Orr H.A., and Coyne J.A. The genetics of adaptation: a reassessment. Am. Nat. 10 (1992) 725-742
70. Ou S.H., and Jennings P.R. Progress in the development of disease-resistant rice. Annu. Rev. Phytopathol. 7 (1969) 383-410
71. Pederson W.L., and Leath S. Pyramiding major genes for resistance to maintain residual effects. Annu. Rev. Phytopathol. 26 (1988) 369-378
72. Pink D.A.C. Strategies using genes for non-durable resistance. Euphytica 1 (2002) 227-236
73. Reyes A., Salazar M., and Granja C. Temperature modifies gene expression in subcuticular epithelial cells of white spot syndrome virus-infected Litopenaeus vannamei. Dev. Comp. Immunol. 31 (2007) 23-29
74. Rolff J., and Siva-Jothy M.T. Invertebrate ecological immunology. Science 301 (2003) 472-475
75. Roush R.T., and McKenzie J.A. Ecological genetics of insecticide and acaricide resistance. Annu. Rev. Entomol. 32 (1987) 361-380
76. Srisuvan T., Noble B.L., Schofield P.J., and Lightner D.V. Comparison of four Taura syndrome virus (TSV) isolates in oral challenge studies with Litopenaeus vannamei unselected or selected for resistance to TSV. Dis. Aquat. Org. 71 (2006) 1-10
77. Stebbing J., Gazzard B., and Douek D.C. Where does HIV live?. New Engl. J. Med. 350 (2004) 1872-1880
78. Teichert-Coddington D.R., and Smitherman R.O. Lack of Response by Tilapia nilotica to Mass Selection for Rapid Early Growth Transactions of the American Fisheries Society 117(3) (1988) 297-300
79. Tian D., Traw M.B., Chen J.Q., Kreitman M., and Bergelson J. Fitness costs of R-gene-mediated resistance in Arabidopsis thaliana. Nature 423 (2003) 74-77
80. Torchin M.E., Lafferty K.D., Dobson A.P., McKenzie V.J., and Kuris A.M. Introduced species and their missing parasites. Nature 421 (2003) 628-630
81. Toyoda K., Collins N.C., Takahashi A., and Shirasu K. Resistance and susceptibility of plants to fungal pathogens. Transgenic Res. 11 (2002) 567-582
82. Vallad G.E., and Goodman R.M. Systemic acquired resistance and induced systemic resistance in conventional agriculture. Crop Sci. 44 (2004) 1920-1934
83. Van der Planck J.E. Plant Diseases: Epidemics and Control (1963), Academic Press, New York 349 pp.
84. Van der Planck J.E. Disease Resistance in Plants (1968), Academic Press, New York 206 pp.
85. Van Hulten M.C.W., Goldbach R.W., and Vlak J.M. Three functionally diverged major structural proteins of white spot syndrome virus evolved by gene duplication. J. Gen. Virol. 81 (2000) 2525-2529
86. Vidal O.M., Granja C.B., Aranguren L.F., Brock J.A., and Salazar M. A profound effect of hyperthermia on survival of Litopenaeus vannamei juveniles infected with White Spot Syndrome Virus. J. World Aquac. Soc. 32 (2001) 364-372
87. Wang W., Wen B., Gasparich G.E., Zhu N., Rong L., Chen J., and Xu Z. A spiroplasma associated with tremor disease in the Chinese mitten crab (Eriocheir sinensis). Microbiology 150 (2004) 3035-3040
88. Wang W., Gu W., Ding Z., Ren Y., Chen J., and Hou Y. A novel Spiroplasma pathogen causing systemic infection in the crayfish Procambarus clarkii (Crustacea: Decapod), in China. FEMS Microbiol. Lett. 249 (2005) 131-137
89. Weber K. Population size and long-term selection. Plant Breed. Rev. 24 (2004) 249-268
90. White B.L., Schofield P.J., Poulos B.T., and Lightner D.V. A laboratory challenge method for estimating Taura Syndrome Virus resistance in selected lines of Pacific White Shrimp Litopenaeus vannamei. J. World Aquac. Soc. 33 (2002) 341-348
91. Witteveldt, J., 2006., On the vaccination of shrimp against white spot syndrome virus. Summary Wageningen University dissertation no. 3882.
92. Wongteerasupaya C., Vickers J.E., Sriurairatana S., Nash G.L., Akarajamorn A., Boosaeng V., Panyim S., Tassanakajon A., Withyachumnarnkul B., and Flegel T.W. A non-occluded, systemic baculovirus that occurs in cells of ectodermal and mesodermal origin and causes high mortality in the black tiger prawn, Penaeus monodon. Dis. Aquat. Org. 21 (1995) 69-77
93. Wyban J.A., Swingle J.S., Sweeney J.N., and Pruder G.D. Development and commercial performance of high health shrimp using specific pathogen free (SPF) broodstock Penaeus vannamei. In: Wyban J.A. (Ed). Proceedings of the Special Session on Shrimp Farming (1992), World Aquaculture Society, Baton Rouge 254-259
94. Zadoks J.C. Epilogue: a summary with personal bias. Euphytica 124 (2002) 259-264
95. Zarain-Herzberg M., and Ascencio-Valle M. Taura Syndrome in Mexico: follow-up study in shrimp farms of Sinaloa. Aquaculture 193 (2001) 1-9
96. Zhan W.B., Wang Y.H., Fryer J.L., Yu K.K., and Fukuda H. White Spot Syndrome Virus infection of cultured shrimp in China. J. Aquat. Anim. Health 10 (1998) 405-410