Protein expression profiling of the shrimp cellular response to white spot syndrome virus infection

Developmental and Comparative Immunology

Volumn 31, Issue 7, 2007, Pages 672-686

  Wang, Hao Ching ^a,b   Wang, Han Ching ^a   Leu, Jiann Horng ^a   Kou, Guang Hsiung ^a   Wang, Andrew H J ^a,b,c   Lo, Chu Fang ^a  

^a NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^b INSTITUTE OF BIOLOGICAL CHEMISTRY   (Taiwan)

^c ACADEMIA SINICA   (Taiwan)

Author keywords

Host response; Protein expression profiling; Proteomic analysis; White spot syndrome virus; WSSV infection

Indexed keywords

COMPLEMENTARY DNA; SUMO PROTEIN;

ARTICLE; BIOINFORMATICS; CALCIUM HOMEOSTASIS; CELLULAR IMMUNITY; CONTROLLED STUDY; DNA LIBRARY; ELECTROSPRAY MASS SPECTROMETRY; ENERGY YIELD; EXPRESSED SEQUENCE TAG; GENE EXPRESSION PROFILING; LIQUID CHROMATOGRAPHY; LITOPENAEUS VANNAMEI; NONHUMAN; NUCLEIC ACID SYNTHESIS; NUCLEOTIDE SEQUENCE; OXYGEN TRANSPORT; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN MODIFICATION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SIGNAL TRANSDUCTION; SUMOYLATION; TWO DIMENSIONAL GEL ELECTROPHORESIS; VIRUS INFECTION; VIRUS PATHOGENESIS; WHITE SPOT SYNDROME VIRUS;

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

EID: 33947732449     PISSN: 0145305X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dci.2006.11.001     Document Type: Article

References (52)

1. 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 Organ 23 (1995) 165-173
2. Flegel T.W. Special topic review: major viral diseases of black tiger prawn (Penaeus monodon) in Thailand. World J Microbiol Biotechnol 13 (1997) 433-442
3. Inouye K., Miwa S., Oseko N., Nakano H., Kimura T., Momoyama K., et al. Mass mortalities of cultured kuruma shrimp Penaeus Japonicus in Japan in 1993 -electron-microscopic evidence of the causative virus. Fish Pathol 29 (1994) 149-158
4. Lo C.F., Leu J.H., Ho C.H., Chen C.H., Peng S.E., Chen Y.T., et al. Detection of baculovirus associated with white spot syndrome (WSBV) in penaeid shrimps using polymerase chain reaction. Dis Aquat Organ 25 (1996) 133-141
5. Momoyama K., Hiraoka M., Nakano H., Koube H., Inouye K., and Oseko N. Mass mortalities of cultured kuruma shrimp, Penaeus japonicus, in Japan in 1993-Histopathological Study. Fish Pathol 29 (1994) 141-148
6. Nakano H., Koube H., Umezawa S., Momoyama K., Hiraoka M., Inouye K., et al. Mass mortalities of cultured kuruma shrimp, Penaeus-Japonicus, in Japan in 1993 -epizootiological survey and infection trials. Fish Pathol 29 (1994) 135-139
7. Takahashi Y., Itami T., Kondo M., Maeda M., Fujii R., Tomonaga S., et al. Electron microscopic evidence of bacilliform virus infection in kuruma shrimp (Penaeus japonicus). Fish Pathol 29 (1994) 121-125
8. Wang C.H., Lo C.F., Leu J.H., Chou C.M., Yeh P.Y., Chou H.Y., et al. Purification and genomic analysis of baculovirus associated with white spot syndrome (WSBV) of Penaeus monodon. Dis Aquat Organ 23 (1995) 239-242
9. Wongteerasupaya C., Vickers J.E., Sriurairatana S., Nash G.L., Akarajamorn A., Boonsaeng V., et al. 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 Organ 21 (1995) 69-77
10. Chen L.L., Wang H.C., Huang C.J., Peng S.E., Chen Y.G., Lin S.J., et al. Transcriptional analysis of the DNA polymerase gene of shrimp white spot syndrome virus. Virology 301 (2002) 136-147
11. van Hulten M.C., Witteveldt J., Peters S., Kloosterboer N., Tarchini R., Fiers M., et al. The white spot syndrome virus DNA genome sequence. Virology 286 (2001) 7-22
12. Yang F., He J., Lin X., Li Q., Pan D., Zhang X., et al. Complete genome sequence of the shrimp white spot bacilliform virus. J Virol 75 (2001) 11811-11820
13. Tsai J.M., Wang H.C., Leu J.H., Hsiao H.H., Wang A.H., Kou G.H., et al. Genomic and proteomic analysis of thirty-nine structural proteins of shrimp white spot syndrome virus. J Virol 78 (2004) 11360-11370
14. Tsai J.M., Wang H.C., Leu J.H., Wang A.H., Zhuang Y., Walker P.J., et al. Identification of the nucleocapsid, tegument, and envelope proteins of the shrimp white spot syndrome virus virion. J Virol 80 (2006) 3021-3029
15. Leu J.H., Tsai J.M., Wang H.C., Wang A.H., Wang C.H., Kou G.H., et al. The unique stacked rings in the nucleocapsid of the white spot syndrome virus virion are formed by the major structural protein VP664, the largest viral structural protein ever found. J Virol 79 (2005) 140-149
16. Valk J.M., Bonami J.R., Flegel T.W., Kou G.H., Lightner D.V., Lo C.F., et al. Nimaviridae. In: Fauquet C.M., Mayo M.A., Maniloff J., Desselberger U., and Ball L.A. (Eds). VIIIth report of the international committee on taxonomy of viruses (2004), Elsevier Press, Amsterdam 187-192
17. Astrofsky K.M., Roux M.M., Klimpel K.R., Fox J.G., and Dhar A.K. Isolation of differentially expressed genes from white spot virus (WSV) infected Pacific blue shrimp (Penaeus stylirostris). Arch Virol 147 (2002) 1799-1812
18. Bangrak P., Graidist P., Chotigeat W., Supamattaya K., and Phongdara A. A syntenin-like protein with postsynaptic density protein (PDZ) domains produced by black tiger shrimp Penaeus monodon in response to white spot syndrome virus infection. Dis Aquat Organ 49 (2002) 19-25
19. Dhar A.K., Dettori A., Roux M.M., Klimpel K.R., and Read B. Identification of differentially expressed genes in shrimp (Penaeus stylirostris) infected with White spot syndrome virus by cDNA microarrays. Arch Virol 148 (2003) 2381-2396
20. Gross P.S., Bartlett T.C., Browdy C.L., Chapman R.W., and 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. Dev Comp Immunol 25 (2001) 565-577
21. He N., Qin Q., and 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 Res 66 (2005) 39-45
22. Pan D., He N., Yang Z., Liu H., and Xu X. Differential gene expression profile in hepatopancreas of WSSV-resistant shrimp (Penaeus japonicus) by suppression subtractive hybridization. Dev Comp Immunol 29 (2005) 103-112
23. Rojtinnakorn J., Hirono I., Itami T., Takahashi Y., and Aoki T. Gene expression in haemocytes of kuruma prawn, Penaeus japonicus, in response to infection with WSSV by EST approach. Fish Shellfish Immunol 13 (2002) 69-83
24. Roux M.M., Pain A., Klimpel K.R., and Dhar A.K. The lipopolysaccharide and beta-1,3-glucan binding protein gene is upregulated in white spot virus-infected shrimp (Penaeus stylirostris). J Virol 76 (2002) 7140-7149
25. Lo C.F., Ho C.H., Chen C.H., Liu K.F., Chiu Y.L., Yeh P.Y., et al. Detection and tissue tropism of white spot syndrome baculovirus (WSBV) in captured brooders of Penaeus monodon with a special emphasis on reproductive organs. Dis Aquat Organ 30 (1997) 53-72
26. Tsai M.F., Kou G.H., Liu H.C., Liu K.F., Chang C.F., Peng S.E., et al. Long-term presence of white spot syndrome virus (WSSV) in a cultivated shrimp population without disease outbreaks. Dis Aquat Org 38 (1999) 107-114
27. Wu J.L., and Muroga K. Apoptosis does not play an important role in the resistance of 'immune' Penaeus japonicus against white spot syndrome virus. J Fish Dis 27 (2004) 15-21
28. Bangrak P., Graidist P., Chotigeat W., and Phongdara A. Molecular cloning and expression of a mammalian homologue of a translationally controlled tumor protein (TCTP) gene from Penaeus monodon shrimp. J Biotechnol 108 (2004) 219-226
29. Luo T., Zhang X., Shao Z., and Xu X. PmAV, a novel gene involved in virus resistance of shrimp Penaeus monodon. FEBS Lett 551 (2003) 53-57
30. Zhang X., Huang C., and Qin Q. Antiviral properties of hemocyanin isolated from shrimp Penaeus monodon. Antiviral Res 61 (2004) 93-99
31. O'Farrell P.H. High resolution two-dimensional electrophoresis of proteins. J Biol Chem 250 (1975) 4007-4021
32. Bjellqvist B., Kristina E.K., Righetti P.G., Gianazza E., Görg A., Westermeier R., et al. Isoelectric focusing in immobilized ph gradients: principle, methodology and some applications. J Biochem Biophys Methods 6 (1982) 317-339
33. Lo C.F., Hsu H.C., Tsai M.F., Ho C.H., Peng S.E., Kou G.H., et al. Specific genomic DNA fragment analysis of different geographical clinical samples of shrimp white spot syndrome virus. Dis Aquat Organ 35 (1999) 175-185
34. Wu J.L., Suzuki K., Arimoto M., Nishizawa T., and Muroga K. Preparation of an inoculum of white spot syndrome virus for challenge tests in Penaeus japonicus. Fish Pathol 37 (2002) 65-69
35. Kanehisa M., and Goto S. KEGG: kyoto encyclopedia of genes and genomes. Nucleic Acids Res 28 (2000) 27-30
36. Kimura N., Shimada N., Fukuda M., Ishijima Y., Miyazaki H., Ishii A., et al. Regulation of cellular functions by nucleoside diphosphate kinases in mammals. J Bioenerg Biomembr 32 (2000) 309-315
37. Narayanan R., and Ramaswami M. Regulation of dynamin by nucleoside diphosphate kinase. J Bioenerg Biomembr 35 (2003) 49-55
38. Cheshenko N., Del Rosario B., Woda C., Marcellino D., Satlin L.M., and Herold B.C. Herpes simplex virus triggers activation of calcium-signaling pathways. J Cell Biol 163 (2003) 283-293
39. 2+-binding chaperone of the endoplasmic reticulum. Int J Biochem Cell Biol 37 (2005) 260-266
40. Rabah G., Popescu R., Cox J.A., Engelborghs Y., and Craescu C.T. Solution structure and internal dynamics of NSCP, a compact calcium-binding protein. FEBS J 272 (2005) 2022-2036
41. Takagi T., and Konishi K. Amino acid sequence of alpha chain of sarcoplasmic calcium binding protein obtained from shrimp tail muscle. J Biochem (Tokyo) 95 (1984) 1603-1615
42. Golshani-Hebroni S.G., and Bessman S.P. Hexokinase binding to mitochondria: a basis for proliferative energy metabolism. J Bioenerg Biomembr 29 (1997) 331-338
43. Pastorino J.G., and Hoek J.B. Hexokinase II: the integration of energy metabolism and control of apoptosis. Curr Med Chem 10 (2003) 1535-1551
44. Bryson J.M., Coy P.E., Gottlob K., Hay N., and Robey R.B. Increased hexokinase activity, of either ectopic or endogenous origin, protects renal epithelial cells against acute oxidant-induced cell death. J Biol Chem 277 (2002) 11392-11400
45. Gottlob K., Majewski N., Kennedy S., Kandel E., Robey R.B., and Hay N. Inhibition of early apoptotic events by Akt/PKB is dependent on the first committed step of glycolysis and mitochondrial hexokinase. Genes Dev 15 (2001) 1406-1418
46. Mackintosh C. Dynamic interactions between 14-3-3 proteins and phosphoproteins regulate diverse cellular processes. Biochem J 381 (2004) 329-342
47. van Hemert M.J., Steensma H.Y., and van Heusden G.P. 14-3-3 proteins: key regulators of cell division, signaling and apoptosis. BioEssays 23 (2001) 936-946
48. Ishitani R., and Chuang D.M. Glyceraldehyde-3-phosphate dehydrogenase antisense oligodeoxynucleotides protect against cytosine arabinonucleoside-induced apoptosis in cultured cerebellar neurons. Neurobiology 93 (1996) 9937-9941
49. Nahlik K.W., Mleczko A.K., Gawlik M.K., and Rokita H.B. Modulation of GAPDH expression and cellular localization after vaccinia virus infection of human adherent monocytes. Acta Biochim Pol 50 (2003) 667-676
50. Lin S.S., Chang S.C., Wang Y.H., Sun C.Y., and Chang M.F. Specific interaction between the hepatitis delta virus RNA and glyceraldehyde 3-phosphate dehydrogenase: an enhancement on ribozyme catalysis. Virology 271 (2000) 46-57
51. Huber S.C., MacKintosh C., and Kaiser W.M. Metabolic enzymes as targets for 14-3-3 proteins. Plant Mol Biol 50 (2002) 1053-1063
52. 2+/calmodulin-dependent manner. J Biol Chem 279 (2004) 35176-35282