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ZIRC
ZFIN ID: ZDB-PUB-110131-35
Activation of cytokine expression occurs through the tnfα/nf-κb-mediated pathway in birnavirus-infected cells
Wang, W.L., Liu, W., Gong, H.Y., Hong, J.R., Lin, C.C., and Wu, J.L.
Date: 2011
Source: Fish & shellfish immunology   31(1): 10-21 (Journal)
Registered Authors: Gong, Hong-Yi, Hong, Jiann-Ruey, Wu, Jen-Leih
Keywords: birnavirus, tumor necrosis factor alpha, NF-κB, cytokine expression
MeSH Terms:
  • Animals
  • Birnaviridae Infections/immunology
  • Birnaviridae Infections/veterinary*
  • Cell Line
  • Cytokines/genetics
  • Cytokines/immunology
  • Cytokines/metabolism*
  • Fish Diseases/immunology*
  • Fish Proteins/genetics
  • Fish Proteins/immunology
  • Fish Proteins/metabolism
  • Gene Expression Profiling
  • Infectious pancreatic necrosis virus/immunology*
  • Metalloproteases/genetics
  • Metalloproteases/immunology
  • Metalloproteases/metabolism*
  • NF-kappa B/genetics
  • NF-kappa B/immunology
  • NF-kappa B/metabolism*
  • Signal Transduction*
  • Tumor Necrosis Factor-alpha/genetics
  • Tumor Necrosis Factor-alpha/immunology
  • Tumor Necrosis Factor-alpha/metabolism*
  • Up-Regulation
  • Zebrafish/genetics
  • Zebrafish/immunology*
  • Zebrafish/metabolism
  • Zebrafish/virology
PubMed: 21272652 Full text @ Fish Shellfish Immunol.
ABSTRACT
The infectious pancreatic necrosis virus (IPNV) belongs to the Birnaviridae family of viruses and causes acute contagious diseases in a number of economically important freshwater and marine fish. In this study, we infected zebrafish embryonic cells (ZF4) with IPNV and analyzed the gene expression patterns of normal and infected cells using quantitative real-time PCR. We identified a number of immune response genes, including ifna, ifng, mx, irf1, irf2, irf4, tnfa, tnfb, il-1b, il-15, il-26, ccl4 and mmp family genes, that are induced after viral infection. Transcriptional regulators, including cebpb, junb, nfkb and stat1, stat4 and stat5, were also upregulated in IPNV-infected cells. In addition, we used Pathway Studio software to identify TNFα as having the greatest downstream influence among these altered genes. Treating virus-infected cells with an siRNA targeting TNFα inhibited NF-κB expression. To further interrupt the TNFα/NF-κB-mediated pathway, the expression levels of cytokines and metalloproteinases were inhibited in IPNV-infected cells. These data suggest that, during IPNV infection, the expression of cytokines and metalloproteinases might be initiated through the TNFα/NF-κB-mediated pathway. The modulation of TNFα/NF-κB-related mechanisms may provide a therapeutic strategy for inhibiting viral infection in teleosts.
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