Litopenaeus vannamei NF-κB is required for WSSV replication

Developmental and Comparative Immunology

Volumn 45, Issue 1, 2014, Pages 156-162

  Qiu, Wei ^a   Zhang, Shuang ^a   Chen, Yong Gui ^a   Wang, Pei Hui ^a   Xu, Xiao Peng ^a   Li, Chao zheng ^a   Chen, Yi Hong ^a   Fan, Wen Zhou ^a   Yan, Hui ^a   Weng, Shao Ping ^a   FrancisChan, Siuming ^b   He, Jian Guo ^a  

^a SUN YAT SEN UNIVERSITY   (China)

^b GUANGDONG OCEAN UNIVERSITY   (China)

Author keywords

Litopenaeus vannamei; LvDorsal; LvRelish; WSSV

Indexed keywords

DOUBLE STRANDED RNA; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; LUCIFERASE; VIRUS ENVELOPE PROTEIN; ARTHROPOD PROTEIN; VP28 PROTEIN, WHITE SPOT SYNDROME VIRUS;

ARTICLE; BINDING SITE; IN VITRO STUDY; IN VIVO STUDY; LIFE CYCLE; LITOPENAEUS VANNAMEI; LUCIFERASE ASSAY; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN EXPRESSION; SHRIMP; UPREGULATION; VIRUS LOAD; VIRUS REPLICATION; WHITE SPOT SYNDROME VIRUS; ANIMAL; GENE EXPRESSION REGULATION; GENETICS; GILL; HOST PATHOGEN INTERACTION; METABOLISM; PENAEIDAE; PHYSIOLOGY; STOMACH MUCOSA; VIROLOGY;

ANIMALS; ARTHROPOD PROTEINS; GASTRIC MUCOSA; GENE EXPRESSION REGULATION, VIRAL; GILLS; HOST-PATHOGEN INTERACTIONS; NF-KAPPA B; PENAEIDAE; PROMOTER REGIONS, GENETIC; UP-REGULATION; VIRAL ENVELOPE PROTEINS; VIRUS REPLICATION; WHITE SPOT SYNDROME VIRUS 1;

EID: 84896462625     PISSN: 0145305X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dci.2014.02.016     Document Type: Article

References (34)

1. Amici C., Belardo G., Rossi A., Santoro M.G. Activation of I kappa b kinase by herpes simplex virus type 1. A novel target for anti-herpetic therapy. J. Biol. Chem. 2001, 276:28759-28766.
2. Diao J., Garces R., Richardson C.D. X protein of hepatitis B virus modulates cytokine and growth factor related signal transduction pathways during the course of viral infections and hepatocarcinogenesis. Cytokine Growth Factor Rev. 2001, 12:189-205.
3. Escobedo-Bonilla C.M., Alday-Sanz V., Wille M., Sorgeloos P., Pensaert M.B., Nauwynck H.J. A review on the morphology, molecular characterization, morphogenesis and pathogenesis of white spot syndrome virus. J. Fish Dis. 2008, 31:1-18.
4. Hiscott J., Nguyen T.L., Arguello M., Nakhaei P., Paz S. Manipulation of the nuclear factor-kappaB pathway and the innate immune response by viruses. Oncogene 2006, 25:6844-6867.
5. Huang X.D., Yin Z.X., Liao J.X., Wang P.H., Yang L.S., Ai H.S., Gu Z.H., Jia X.T., Weng S.P., Yu X.Q., He J.G. Identification and functional study of a shrimp Relish homologue. Fish Shellfish Immunol. 2009, 27:230-238.
6. Huang X.D., Zhao L., Zhang H.Q., Xu X.P., Jia X.T., Chen Y.H., Wang P.H., Weng S.P., Yu X.Q., Yin Z.X., He J.G. Shrimp NF-kappaB binds to the immediate-early gene ie1 promoter of white spot syndrome virus and upregulates its activity. Virology 2010, 406:176-180.
7. Huang X.D., Yin Z.X., Jia X.T., Liang J.P., Ai H.S., Yang L.S., Liu X., Wang P.H., Li S.D., Weng S.P., Yu X.Q., He J.G. Identification and functional study of a shrimp dorsal homologue. Dev. Comp. Immunol. 2010, 34:107-113.
8. Kim C.S., Kosuke Z., Nam Y.K., Kim S.K., Kim K.H. Protection of shrimp (Penaeus chinensis) against white spot syndrome virus (WSSV) challenge by double-stranded RNA. Fish Shellfish Immunol. 2007, 23:242-246.
9. Li C., Chen Y.X., Zhang S., Lu L., Chen Y.H., Chai J., Weng S., Chen Y.G., He J., Xu X. Identification, characterization, and function analysis of the Cactus gene from Litopenaeus vannamei. PLoS One 2012, 7:e49711.
10. Li F., Li M., Ke W., Ji Y., Bian X., Yan X. Identification of the immediate-early genes of white spot syndrome virus. Virology 2009, 385:267-274.
11. Li F., Yan H., Wang D., Priya T.A., Li S., Wang B., Zhang J., Xiang J. Identification of a novel relish homolog in Chinese shrimp Fenneropenaeus chinensis and its function in regulating the transcription of antimicrobial peptides. Dev. Comp. Immunol. 2009, 33:1093-1101.
12. Li F., Wang D., Li S., Yan H., Zhang J., Wang B., Zhang J., Xiang J. A Dorsal homolog (FcDorsal) in the Chinese shrimp Fenneropenaeus chinensis is responsive to both bacteria and WSSV challenge. Dev. Comp. Immunol. 2010, 34:874-883.
13. Lin Y.R., Hung H.C., Leu J.H., Wang H.C., Kou G.H., Lo C.F. The role of aldehyde dehydrogenase and hsp70 in suppression of white spot syndrome virus replication at high temperature. J. Virol. 2011, 85:3517-3525.
14. Liu W.J., Chang Y.S., Wang C.H., Kou G.H., Lo C.F. Microarray and RT-PCR screening for white spot syndrome virus immediate-early genes in cycloheximide-treated shrimp. Virology 2005, 334:327-341.
15. Liu W.J., Chang Y.S., Wang A.H., Kou G.H., Lo C.F. White spot syndrome virus annexes a shrimp STAT to enhance expression of the immediate-early gene ie1. J. Virol. 2007, 81:1461-1471.
16. Liu W.J., Chang Y.S., Wang H.C., Leu J.H., Kou G.H., Lo C.F. Transactivation, dimerization, and DNA-binding activity of white spot syndrome virus immediate-early protein IE1. J. Virol. 2008, 82:11362-11373.
17. Liu W.J., Chang Y.S., Huang W.T., Chen I.T., Wang K.C., Kou G.H., Lo C.F. Penaeus monodon TATA box-binding protein interacts with the white spot syndrome virus transactivator IE1 and promotes its transcriptional activity. J. Virol. 2011, 85:6535-6547.
18. Mogensen T.H., Paludan S.R. Molecular pathways in virus-induced cytokine production. Microbiol. Mol. Biol. Rev. 2001, 65:131-150.
19. Pahl H.L., Baeuerle P.A. The ER-overload response: activation of NF-kappa B. Trends Biochem. Sci. 1997, 22:63-67.
20. Pfaffl M.W. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001, 29:e45.
21. Robalino J., Browdy C.L., Prior S., Metz A., Parnell P., Gross P., Warr G. Induction of antiviral immunity by double-stranded RNA in a marine invertebrate. J. Virol. 2004, 78:10442-10448.
22. Sakakibara S., Sakakibara K., Tosato G. NF-kappaB activation stimulates transcription and replication of retrovirus XMRV in human B-lineage and prostate carcinoma cells. J. Virol. 2011, 85:3179-3186.
23. Sanchez-Paz A. White spot syndrome virus: an overview on an emergent concern. Vet. Res. 2010, 41:43.
24. Santoro M.G., Rossi A., Amici C. NF-kappaB and virus infection: who controls whom. EMBO J. 2003, 22:2552-2560.
25. Sugano N., Chen W., Roberts M.L., Cooper N.R. Epstein-Barr virus binding to CD21 activates the initial viral promoter via NF-kappaB induction. J. Exp. Med. 1997, 186:731-737.
26. Surabhi R.M., Gaynor R.B. RNA interference directed against viral and cellular targets inhibits human immunodeficiency virus type 1 replication. J. Virol. 2002, 76:12963-12973.
27. Vallabhapurapu S., Karin M. Regulation and function of NF-kappaB transcription factors in the immune system. Annu. Rev. Immunol. 2009, 27:693-733.
28. Wan F., Lenardo M.J. The nuclear signaling of NF-kappaB: current knowledge, new insights, and future perspectives. Cell Res. 2010, 20:24-33.
29. Wang P.H., Gu Z.H., Wan D.H., Zhang M.Y., Weng S.P., Yu X.Q., He J.G. The shrimp NF-kappaB pathway is activated by white spot syndrome virus (WSSV) 449 to facilitate the expression of WSSV069 (ie1), WSSV303 and WSSV371. PLoS One 2011, 6:e24773.
30. Wang P.H., Wan D.H., Gu Z.H., Deng X.X., Weng S.P., Yu X.Q., He J.G. Litopenaeus vannamei tumor necrosis factor receptor-associated factor 6 (TRAF6) responds to Vibrio alginolyticus and white spot syndrome virus (WSSV) infection and activates antimicrobial peptide genes. Dev. Comp. Immunol. 2011, 35:105-114.
31. Wang Y.G., Hassan M.D., Shariff M., Zamri S.M., Chen X. Histopathology and cytopathology of white spot syndrome virus (WSSV) in cultured Penaeus monodon from peninsular Malaysia with emphasis on pathogenesis and the mechanism of white spot formation. Dis. Aquat. Organ. 1999, 39:1-11.
32. West M.J., Lowe A.D., Karn J. Activation of human immunodeficiency virus transcription in T cells revisited: NF-kappaB p65 stimulates transcriptional elongation. J. Virol. 2001, 75:8524-8537.
33. Yang F., He J., Lin X., Li Q., Pan D., Zhang X., Xu X. Complete genome sequence of the shrimp white spot bacilliform virus. J. Virol. 2001, 75:11811-11820.
34. Zhang S., Li C.Z., Yan H., Qiu W., Chen Y.G., Wang P.H., Weng S.P., He J.G. Identification and function of myeloid differentiation factor 88 (MyD88) in Litopenaeus vannamei. PLoS One 2012, 7:e47038.