Journal of Virology · 2010 · 63 citations · 40 references
Life SciencesInfectious DiseasesMolecular BiologyHost-pathogen InteractionsMolecular VirologyVirologyHost-virus InteractionsPathogen Virulence FactorsViral InfectionsViral PathogenesisVirulence Gene RegulationVirus-host InteractionsAntiviral Signaling PathwaysNf-kappa B-dependent TranscriptionNf-κb SignalingNuclear Factor Kappa B SignalingNuclear Translocation Of Transcription FactorsViral Transcription FactorsViral Virulence FactorsVirulence Factor Regulation
Orf virus (ORFV), the type member of the genus Parapoxvirus of the Poxviridae, has evolved novel strategies (proteins and/or mechanisms of action) to modulate host cell responses regulated by the nuclear factor-κB (NF-κB) signaling pathway. Here, we present data indicating that ORFV ORFV121, a gene unique to parapoxviruses, encodes a novel viral NF-κB inhibitor that binds to and inhibits the phosphorylation and nuclear translocation of NF-κB-p65. The infection of cells with an ORFV121 deletion mutant virus (OV-IA82Δ121) resulted in increased NF-κB-mediated gene transcription, and the expression of ORFV121 in cell cultures significantly suppressed NF-κB-regulated reporter gene expression. ORFV ORFV121 physically interacts with NF-κB-p65 in the cell cytoplasm, thus providing a mechanism for the inhibition of NF-κB-p65 phosphorylation and nuclear translocation. Notably, the deletion of ORFV121 from the viral genome markedly decreased ORFV virulence and disease pathogenesis in sheep, indicating that ORFV121 is a virulence determinant for ORFV in the natural host.
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NF-κB RelA Phosphorylation Regulates RelA Acetylation
Lin‐Feng Chen, Samuel A. Williams, Yajun Mu et al. · Molecular and Cellular Biology · 2005 · 437 citations · Full text