Gill-associated virus and recombinant protein vaccination in Penaeus monodon

Aquaculture

Volumn 308, Issue 3-4, 2010, Pages 82-88

  Underwood, Darren J ^a   Cowley, Jeff A ^b   Sellars, Melony J ^b   Barnes, Andrew C ^a   van Hulten, Marielle C W ^a   Johnson, Karyn N ^a  

^a UNIVERSITY OF QUEENSLAND   (Australia)

^b CSIRO   (Australia)

Author keywords

Black Tiger Shrimp (Penaeus monodon); Envelope glycoproteins; Gill associated virus; Invertebrate immunity; Nucleocapsid

Indexed keywords

ADAPTATION; BACTERIUM; DISEASE RESISTANCE; IMMUNE RESPONSE; IMMUNITY; MORTALITY; PRAWN CULTURE; PROTEIN; RECOMBINATION; VACCINATION; VIRUS;

ANIMALIA; BACTERIA (MICROORGANISMS); CRUSTACEA; DECAPODA (CRUSTACEA); GILL-ASSOCIATED VIRUS; INVERTEBRATA; PENAEIDAE; PENAEUS MONODON; SHRIMP WHITE SPOT SYNDROME VIRUS; VERTEBRATA;

EID: 77957351183     PISSN: 00448486     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.aquaculture.2010.08.027     Document Type: Article

References (53)

1. Amend D.F. Potency testing of fish vaccines. Developments in Biological Standardization 1981, 49:447-454.
2. Attasart P., Kaewkhaw R., Chimwai C., Kongphom U., Namramoon O., Panyim S. Inhibition of white spot syndrome virus replication in Penaeus monodon by combined silencing of viral rr2 and shrimp PmRab7. Virus Research 2009, 145(1):127-133.
3. Caipang C.M.A., Verjan N., Ooi E.L., Kondo H., Hirono I., Aoki T., Kiyono H., Yuki Y. Enhanced survival of shrimp, Penaeus (Marsupenaeus) japonicus from white spot syndrome disease after oral administration of recombinant VP28 expressed in Brevibacillus brevis. Fish & Shellfish Immunology 2008, 25(3):315-320.
4. Callinan R.B., Jiang L. Fatal, virus-associated peripheral neuropathy and retinopathy in farmed Penaeus monodon in eastern Australia. II. Outbreak descriptions. Diseases of Aquatic Organisms 2003, 53:195-202.
5. Carius H.J., Little T.J., Ebert D. Genetic variation in a host-parasite association: potential for coevolution and frequency-dependent selection. Evolution 2001, 55(6):1136-1145.
6. Cowley J.A., Walker P.J. The complete genome sequence of gill-associated virus of Penaeus monodon prawns indicates a gene organisation unique among nidoviruses. Archives of Virology 2002, 147(10):1977-1987.
7. Cowley J.A., Dimmock C.M., Spann K.M., Walker P.J. Gill-associated virus of Penaeus monodon prawns: an invertebrate virus with ORF1a and ORF1b genes related to arteri- and coronaviruses. Journal of General Virology 2000, 81(6):1473-1484.
8. Cowley J.A., Hall M.R., Cadogan L.C., Spann K.M., Walker P.J. Vertical transmission of gill-associated virus (GAV) in the black tiger prawn Penaeus monodon. Diseases of Aquatic Organisms 2002, 50(2):95-104.
9. Cowley J.A., Cadogan L.C., Spann K.M., Sittidilokratna N., Walker P.J. The gene encoding the nucleocapsid protein of gill-associated nidovirus of Penaeus monodon prawns is located upstream of the glycoprotein gene. Journal of Virology 2004, 78(16):8935-8941.
10. Cowley J.A., Cadogan L.C., Wongteerasupaya C., Hodgson R.A.J., Boonsaeng V., Walker P.J. Multiplex RT-nested PCR differentiation of gill-associated virus (Australia) from yellow head virus (Thailand) of Penaeus monodon. Journal of Virological Methods 2004, 117(1):49-59.
11. Cowley J.A., McCulloch R.J., Rajendran K.V., Cadogan L.C., Spann K.M., Walker P.J. RT-nested PCR detection of Mourilyan virus in Australian Penaeus monodon and its tissue distribution in healthy and moribund prawns. Diseases of Aquatic Organisms 2005, 66(2):91-104.
12. de la Vega E., Degnan B.M., Hall M.R., Cowley J.A., Wilson K.J. Quantitative real-time RT-PCR demonstrates that handling stress can lead to rapid increases of gill-associated virus (GAV) infection levels in Penaeus monodon. Diseases of Aquatic Organims 2004, 59(3):195-203.
13. de la Vega E., O'Leary N.A., Shockey J.E., Robalino J., Payne C., Browdy C.L., Warr G.W., Gross P.S. Anti-lipopolysaccharide factor in Litopenaeus vannamei (LvALF): a broad spectrum antimicrobial peptide essential for shrimp immunity against bacterial and fungal infection. Molecular Immunology 2008, 45(7):1916-1925.
14. Dhar A.K., Roux M.M., Klimpel K.R. Quantitative assay for measuring the Taura syndrome virus and yellow head virus load in shrimp by real-time RT-PCR using SYBR Green chemistry. Journal of Virological Methods 2002, 104(1):69-82.
15. Dhar A.K., Bowers R.M., Licon K.S., Veazey G., Read B. Validation of reference genes for quantitative measurement of immune gene expression in shrimp. Molecular Immunology 2009, 46(8-9):1688-1695.
16. Ding S.-W., Voinnet O. Antiviral immunity directed by small RNAs. Cell 2007, 130(3):413-426.
17. Du H., Xu Z., Wu X., Li W., Dai W. Increased resistance to white spot syndrome virus in Procambarus clarkii by injection of envelope protein VP28 expressed using recombinant baculovirus. Aquaculture 2006, 260(1-4):39-43.
18. Virus Taxonomy: Classification and Nomenclature of Viruses 2005, Elsevier Academic Press. C. Fauquet, M. Mayo, M. Maniloff, U. Desselberger, L. Ball (Eds.).
19. Flegel T.W. Major viral diseases of the black tiger prawn (Penaeus monodon) in Thailand. World Journal of Microbiology and Biotechnology 1997, 13(4):433-442.
20. Flegel T.W. Update on viral accommodation, a model for host-viral interaction in shrimp and other arthropods. Developmental & Comparative Immunology 2007, 31(3):217-231.
21. Hannon G.J. RNA interference. Nature 2002, 418(6894):244-251.
22. Hoffmann J.A. The immune response of Drosophila. Nature 2003, 426:33-38.
23. Jitrapakdee S., Unajak S., Sittidilokratna N., Hodgson R.A., Cowley J.A., Walker P.J., Panyim S., Boonsaeng V. Identification and analysis of gp116 and gp64 structural glycoproteins of yellow head nidovirus of Penaeus monodon shrimp. Journal of General Virology 2003, 84(Pt 4):863-873.
24. Johnson K.N., van Hulten M.C.W., Barnes A.C. "Vaccination" of shrimp against viral pathogens: phenomenology and underlying mechanisms. Vaccine 2008, 26(38):4885-4892.
25. Kurtz J. Specific memory within innate immune systems. Trends in Immunology 2005, 26(4):186-192.
26. Kurtz J., Armitage S.A.O. Alternative adaptive immunity in invertebrates. Trends in Immunology 2006, 27(11):493-496.
27. Kurtz J., Franz K. Innate defence: evidence for memory in invertebrate immunity. Nature 2003, 425(6953):37-38.
28. Lightner D.V. A Handbook of Shrimp Pathology and Diagnostic Procedures for Diseases of Cultured Penaeid Shrimp 1996, Baton Rouge, LA.
29. Little T.J., Kraaijeveld A.R. Ecological and evolutionary implications of immunological priming in invertebrates. Trends in Ecology & Evolution 2004, 19(2):58-60.
30. Liu H., Jiravanichpaisal P., Soderhall I., Cerenius L., Soderhall K. Antilipopolysaccharide factor interferes with white spot syndrome virus replication in vitro and in vivo in the crayfish Pacifastacus leniusculus. Journal of Virology 2006, 80(21):10365-10371.
31. Liu Y.-C., Li F.-H., Dong B., Wang B., Luan W., Zhang X.-J., Zhang L.-S., Xiang J.-H. Molecular cloning, characterization and expression analysis of a putative C-type lectin (Fclectin) gene in Chinese shrimp Fenneropenaeus chinensis. Molecular Immunology 2007, 44(4):598-607.
32. Liu H., Soderhall K., Jiravanichpaisal P. Antiviral immunity in crustaceans. Fish & Shellfish Immunology 2009, 27(2):79-88.
33. Luo T., Zhang X., Shao Z., Xu X. PmAV, a novel gene involved in virus resistance of shrimp Penaeus monodon. FEBS Letters 2003, 551(1-3):53-57.
34. Ma T.H.T., Tiu S.H.K., He J.-G., Chan S.-M. Molecular cloning of a C-type lectin (LvLT) from the shrimp Litopenaeus vannamei: early gene down-regulation after WSSV infection. Fish & Shellfish Immunology 2007, 23(2):430-437.
35. Namikoshi A., Wu J.L., Yamashita T., Nishizawa T., Nishioka T., Arimoto M., Muroga K. Vaccination trials with Penaeus japonicus to induce resistance to white spot syndrome virus. Aquaculture 2004, 229(1-4):25-35.
36. Ongvarrasopone C., Chanasakulniyom M., Sritunyalucksana K., Panyim S. Suppression of PmRab7 by dsRNA inhibits WSSV or YHV infection in shrimp. Marine Biotechnology 2008, 10(4):374-381.
37. Owens L., Hall-Mendelin S. Recent advances in Australian penaeid diseases and pathology. Advances in Tropical Aquaculture 1990, 9:103-112.
38. Pham L.N., Dionne M.S., Shirasu-Hiza M., Schneider D.S. A specific primed immune response in Drosophila is dependent on phagocytes. PLoS Pathogens 2007, 3(3):e26.
39. Robalino J., Almeida J.S., McKillen D., Colglazier J., Trent H.F., Chen Y.A., Peck M.E.T., Browdy C.L., Chapman R.W., Warr G.W., Gross P.S. Insights into the immune transcriptome of the shrimp Litopenaeus vannamei: tissue-specific expression profiles and transcriptomic responses to immune challenge. Physiological Genomics 2007, 29(1):44-56.
40. Rout N., Kumar S., Jaganmohan S., Murugan V. DNA vaccines encoding viral envelope proteins confer protective immunity against WSSV in black tiger shrimp. Vaccine 2007, 25(15):2778-2786.
41. Schneider D.S. How and why does a fly turn it's immune system off?. PLoS Biology 2007, 5(9):e247.
42. Soowannayan C., Cowley J.A., Pearson R.D., Wallis T.P., Gorman J.J., Michalski W.P., Walker P.J. Glycosylation of gp116 and gp64 envelope proteins of yellow head virus of Penaeus monodon shrimp. Journal of General Virology 2010, 91:2463-2473.
43. Spann K.M., Lester R.J.G. Viral diseases of penaeid shrimp with particular reference to four viruses recently found in shrimp from Queensland. World Journal of Microbiology and Biotechnology 1997, 13(4):419-426.
44. Spann K.M., Cowley J.A., Walker P.J., Lester R.J.G. A yellow-head-like virus from Penaeus monodon cultured in Australia. Diseases of Aquatic Organisms 1997, 31:169-179.
45. Spann K.M., Donaldson A.R., Cowley J.A., Walker P.J. Differences in the susceptibility of some penaeid prawn species to gill-associated virus (GAV) infection. Diseases of Aquatic Organisms 2000, 42:221-225.
46. van Hulten M.C.W., Westenberg M., Goodall S.D., Vlak J.M. Identification of two major virion protein genes of white spot syndromevirus of shrimp. Virology 2000, 266(2):227-236.
47. van Hulten M.C.W., Witteveldt J., Snippe M., Vlak J.M. White spot syndrome virus envelope protein VP28 is involved in the systemic infection of shrimp. Virology 2001, 285(2):228-233.
48. Wang Q., Poulos B.T., Lightner D.V. Protein analysis of geographic isolates of shrimp white spot syndrome virus. Archives of Virology 2000, 145(2):263-274.
49. Witteveldt J., Cifuentes C.C., Vlak J.M., van Hulten M.C.W. Protection of Penaeus monodon against white spot syndrome virus by oral vaccination. Journal of Virology 2004, 78(4):2057-2061.
50. Witteveldt J., Vlak J.M., van Hulten M.C.W. Protection of Penaeus monodon against white spot syndrome virus using a WSSV subunit vaccine. Fish & Shellfish Immunology 2004, 16(5):571-579.
51. Wu J.L., Nishioka T., Mori K., Nishizawa T., Muroga K. A time-course study on the resistance of Penaeus japonicus induced by artificial infection with white spot syndrome virus. Fish & Shellfish Immunology 2002, 13(5):391-403.
52. Yodmuang S., Tirasophon W., Roshorm Y., Chinnirunvong W., Panyim S. YHV-protease dsRNA inhibits YHV replication in Penaeus monodon and prevents mortality. Biochemical and Biophysical Research Communications 2006, 341(2):351-356.
53. Zhao Z.-Y., Yin Z.-X., Xu X.-P., Weng S.-P., Rao X.-Y., Dai Z.-X., Luo Y.-W., Yang G., Li Z.-S., Guan H.-J., Li S.-D., Chan S.-M., Yu X.-Q., He J.-G. A novel C-type lectin from the shrimp Litopenaeus vannamei possesses anti-white spot syndrome virus activity. Journal of Virology 2009, 83(1):347-356.