Survivability of Penaeus monodon during white spot syndrome virus infection and its correlation with immune related genes

Aquaculture

Volumn 380-383, Issue , 2013, Pages 84-90

  Jeswin, J ^a   Anju, A ^a   Thomas, P C ^a   Paulton, M P ^a   Vijayan, K K ^a  

^a CENTRAL MARINE FISHERIES RESEARCH INSTITUTE   (India)

Author keywords

Antiviral defence; Biomarker; Gene expression; Penaeus monodon; White spot syndrome virus

Indexed keywords

ANTIMICROBIAL ACTIVITY; BIOMARKER; CRUSTACEAN; DISEASE CONTROL; DISEASE RESISTANCE; ENZYME ACTIVITY; GENE EXPRESSION; IMMUNE RESPONSE; MOLECULAR ANALYSIS; SURVIVAL; VIRAL DISEASE;

ANIMALIA; CRUSTACEA; DECAPODA (CRUSTACEA); PENAEUS MONODON; SHRIMP WHITE SPOT SYNDROME VIRUS;

EID: 84871532132     PISSN: 00448486     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.aquaculture.2012.12.004     Document Type: Article

References (53)

1. Ai H.S., Huang Y.C., Li S.D., Weng S.P., Yu X.Q., He J.G. Characterization of a prophenoloxidase from hemocytes of the shrimp Litopenaeus vannamei that is down-regulated by white spot syndrome virus. Fish & Shellfish Immunology 2008, 25:28-39.
2. Amparyup P., Charoensapsri W., Tassanakajon A. Two prophenoloxidases are important for the survival of Vibrio harveyi challenged shrimp Penaeus monodon. Developmental and Comparative Immunology 2009, 33:247-256.
3. Bachere E. Anti-infectious immune effectors in marine invertebrates: potential tools for disease control in larviculture. Aquaculture 2003, 227:427-438.
4. Bachere E., Gueguen Y., Gonzalez M., de Lorgeril J., Garnier J., Romestand B. Insights into the anti-microbial defense of marine invertebrates: the penaeid shrimps and the oyster Crassostrea gigas. Immunology Reviews 2004, 198:149-168.
5. Bayne C.J. Phagocytosis and non-self recognition in invertebrates. BioScience 1990, 40:723-731.
6. Cerenius L., Soderhall K. The prophenoloxidase-activating system in invertebrates. Immunology Reviews 2004, 198:116-126.
7. Chang P.S., Chen H.C., Wang Y.C. Detection of white spot syndrome associated baculovirus WSBV in experimentally infected wild shrimps, crabs and lobsters by in situ hybridization. Aquaculture 1998, 164:23-43.
8. Chen S.C., Jones D.H., Fynan E.F., Farrar G.H., Clegg J.C., Greenberg H.B., Herrmann J.E. Protective immunity induced by oral immunization with a rotavirus DNA vaccine encapsulated in microparticles. Journal of Virology 1997, 72:5757-5761.
9. Chipman D.M., Sharon N. Mechanism of lysozyme action. Science 1969, 165:454-465.
10. Decker H., Rimke T. Tarantula hemocyanin shows phenoloxidase activity. Journal of Biological Chemistry 1998, 273:25889-25892.
11. Destoumieux D., Bulet P., Loew D., Van Dorsselaer A., Rodriguez J., Bachere E. Penaeidins, a new family of antimicrobial peptides isolated from the shrimp Penaeus vannamei (Decapoda). Journal of Biological Chemistry 1997, 272:28398-28406.
12. Destoumieux-Garzon D., Saulnier D., Garnier J., Jouffrey C., Bulet P., Bachere E. Crustacean immunity. Antifungal peptides are generated from the C terminus of shrimp hemocyanin in response to microbial challenge. Journal of Biological Chemistry 2001, 276:47070-47077.
13. Dhar A.K., Dettori A., Roux M.M., Klimpel K.R., Read B. Identification of differentially expressed genes in shrimp (Penaeus stylirostris) infected with white spot syndrome virus by cDNA microarrays. Archives of Virology 2003, 148:2381-2396.
14. Gross P.S., Bartlett T.C., Browdy C.L., Chapman R.W., Warr G.W. Immune gene discovery by expressed sequence tag analysis of hemocytes and hepatopancreas in the Pacific White Shrimp, Litopenaeus vannamei, and the Atlantic White Shrimp, L. setiferus. Developmental and Comparative Immunology 2001, 25:565-577.
15. He N., Qin Q., Xu X. Differential profile of genes expressed in hemocytes of white spot syndrome virus-resistant shrimp (Penaeus japonicus) by combining suppression subtractive hybridization and differential hybridization. Antiviral Research 2005, 66:39-45.
16. Ji P.F., Yao C.L., Wang Z.Y. Immune response and gene expression in shrimp (Litopenaeus vannamei) hemocytes and hepatopancreas against some pathogen-associated molecular patterns. Fish & Shellfish Immunology 2009, 27:563-570.
17. Johansson M.W., Keyser P., Sritunyalucksana K., Soderhall K. Crustacean haemocytes and haematopoiesis. Aquaculture 2000, 191:45-52.
18. Kimura T., Yamano K., Nakano H., Momoyama K., Hiraoka M., Inouye K. Detection of penaeid rod-shaped DNA virus (PRDV) by PCR. Fish Pathology 1996, 31:93-98.
19. Lee S.Y., Soderhall K. Early events in crustacean innate immunity. Fish & Shellfish Immunology 2002, 12:421-437.
20. Lee S.Y., Lee B.L., Soderhall K. Processing of an antibacterial peptide from hemocyanin of the freshwater crayfish Pacifastacus leniusculus. Journal of Biological Chemistry 2003, 278:7927-7933.
21. Lehnert S.A., Wilson K.J., Byrne K., Moore S.S. Tissue-specific expressed sequence tags from the black tiger shrimp Penaeus monodon. Marine Biotechnology (New York, N.Y.) 1999, 1:465-476.
22. Lei K., Li F., Zhang M., Yang H., Luo T., Xu X. Difference between hemocyanin subunits from shrimp Penaeus japonicus in anti-WSSV defense. Developmental and Comparative Immunology 2008, 32:808-813.
23. Leu J.H., Chang C.C., Wu J.L., Hsu C.W., Hirono I., Aoki T., Juan H.F., Lo C.F., Kou G.H., Huang H.C. Comparative analysis of differentially expressed genes in normal and white spot syndrome virus infected Penaeus monodon. BMC Genomics 2007, 8:120-134.
24. Lightner D.V. A handbook of Shrimp Pathology and Diagnostic Procedures for Disease of Cultured Penaeid Shrimp 1996, World Aquaculture Society, Baton Rouge, LA.
25. Lin K.C., Wey M.T., Kan L.S., Shiua D. Characterization of the interactions of lysozyme with DNA by surface plasmon resonance and circular dichroism spectroscopy. Applied Biochemistry and Biotechnology 2009, 53:631-641.
26. 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, 44:598-607.
27. 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., Kou G.H. White spot syndrome baculovirus (WSBV) detected in cultured and captured shrimp, crabs and other arthropods. Diseases of Aquatic Organisms 1996, 27:215-226.
28. Losso L.N., Nakai S., Charter E.A. Lysozyme. Natural food animicrobial systems 2000, 185-210. CRC Press, New York. A. Naidu (Ed.).
29. Luo T., Zhang X., Shao Z., Xu X. PmAV, a novel gene involved in virus resistance of shrimp Penaeus monodon. FEBS Letters 2003, 551:53-57.
30. Luo T., Yang H., Li F., Zhang X., Xu X. Purification, characterization and cDNA cloning of a novel lipopolysaccharide-binding lectin from the shrimp Penaeus monodon. Developmental and Comparative Immunology 2006, 30:607-617.
31. Mai W.J., Wang W.N. Protection of blue shrimp (Litopenaeus stylirostris) against the white spot syndrome virus (WSSV) when injected with shrimp lysozyme. Fish & Shellfish Immunology 2010, 28:727-733.
32. Munoz M., Vandenbulcke F., Saulnier D., Bachere E. Expression and distribution of penaeidin antimicrobial peptides are regulated by haemocyte reactions in microbial challenged shrimp. European Journal of Biochemistry 2002, 269:2678-2689.
33. Pan D., He N., Yang Z., Liu H., Xu X. Differential gene expression profile in hepatopancreas of WSSV-resistant shrimp (Penaeus japonicus) by suppression subtractive hybridization. Developmental and Comparative Immunology 2005, 29:103-112.
34. Pongsomboon S., Tang S., Boonda S., Aoki T., Hirono I., Tassanakajon A. A cDNA microarray approach for analyzing transcriptional changes in Penaeus monodon after infection by pathogens. Fish & Shellfish Immunology 2011, 30:439-446.
35. Rojtinnakorn J., Hirono I., Itami T., Takahashi Y., Aoki T. Gene expression in haemocytes of kuruma prawn, Penaeus japonicus, in response to infection with WSSV by EST approach. Fish & Shellfish Immunology 2002, 13:69-83.
36. Roux M.M., Pain A., Klimpel K.R., Dhar A.K. The lipopolysaccharide and beta-1,3-glucan binding protein gene is upregulated in white spot virus-infected shrimp (Penaeus stylirostris). Journal of Virology 2002, 76:7140-7149.
37. Sahul Hameed A.S., Yoganandhan K., Sathish S., Murugan V., Rasheed M., Jayaraman Kunthala Experimental pathogenicity of white spot syndrome virus (WSSV) in two freshwater crabs (Partelphusa hydrodomous and P. pulvinata). Aquaculture 2001, 201:179-186.
38. Sahul Hameed A.S., Balasubramanian G., Syed Musthaq S., Yoganandhan K. Experimental infection of twenty species of Indian marine crabs with white spot syndrome virus (WSSV). Diseases of Aquatic Organisms 2003, 57:157-161.
39. Smith V.J., Fernandes J.M., Kemp G.D., Hauton C. Crustins: enigmatic WAP domain containing antibacterial proteins from crustaceans. Developmental and Comparative Immunology 2008, 32:758-772.
40. Soderhall K. Invertebrate immunity. Developmental and Comparative Immunology 1999, 23:263-266.
41. Soderhall K., Cerenius L. Role of the prophenoloxidase activating system in invertebrate immunity. Current Opinion in Immunology 1998, 10:23-28.
42. Soonthornchai W., Rungrassamee W., Karoonuthaisiri N., Jarayabhand P., Klinbunga S., Soderhall K., Jiravanichpaisal P. Expression of immune-related genes in the digestive organ of shrimp, Penaeus monodon, after an oral infection by Vibrio harveyi. Developmental and Comparative Immunology 2010, 34:19-28.
43. Sritunyalucksana K., Soderhall K. The proPO and clotting system in crustaceans. Aquaculture 2000, 191:53-69.
44. Supungul P., Tang S., Maneeruttanarungroj C., Rimphanitchayakit V., Hirono I., Aoki T., Tassanakajon A. Cloning, expression and antimicrobial activity of crustinPm1, a major isoform of crustin, from the black tiger shrimp Penaeus monodon. Developmental and Comparative Immunology 2008, 32:61-70.
45. Tassanakajon A., Klinbunga S., Paunglarp N., Rimphanitchayakit V., Udomkit A., Jitrapakdee S., Sritunyalucksana K., Phongdara A., Pongsomboon S., Supungul P., Tang S., Kuphanumart K., Pichyangkura R., Lursinsap C. Penaeus monodon gene discovery project: the generation of an EST collection and establishment of a database. Gene 2006, 384:104-112.
46. Van De Braak C.B., Botterblom M.H., Taverne N., van Muiswinkel W.B., Rombout J.H., van der Knaap W.P. The roles of haemocytes and the lymphoid organ in the clearance of injected Vibrio bacteria in Penaeus monodon shrimp. Fish & Shellfish Immunology 2002, 13:293-309.
47. Wang Y.C., Chang P.S., Chen H.Y. Tissue distribution of prophenoloxidase transcript in the Pacific white shrimp Litopenaeus vannamei. Fish & Shellfish Immunology 2006, 20:414-418.
48. Wang B., Li F., Luan W., Xie Y., Zhang C., Luo Z., Gui L., Yan H., Xiang J. Comparison of gene expression profiles of Fenneropenaeus chinensis challenged with WSSV and Vibrio. Marine Biotechnology 2008, 10:664-675.
49. Wongpanya R., Aoki T., Hirono I., Yasuike M., Tassanakajon A. Analysis of gene expression in haemocytes of Shrimp Penaeus monodon challenged with white spot syndrome virus by cDNA microarray. ScienceAsia 2007, 33:165-174.
50. Woramongkolchai N., Supungul P., Tassanakajon A. The possible role of penaeidin5 from the black tiger shrimp, Penaeus monodon, in protection against viral infection. Developmental and Comparative Immunology 2011, 35:530-536.
51. Zhang X., Huang C., Qin Q. Antiviral properties of hemocyanin isolated from shrimp Penaeus monodon. Antiviral Research 2004, 61(2):93-99.
52. Zhao Z.Y., Yin Z.X., Weng S.P., Guan H.J., Li S.D., Xing K., Chan S.M., He J.G. Profiling of differentially expressed genes in hepatopancreas of white spot syndrome virus-resistant shrimp (Litopenaeus vannamei) by suppression subtractive hybridisation. Fish & Shellfish Immunology 2007, 22:520-553.
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, 83:347-356.