| Literature DB >> 18588927 |
Cheng-Wen Lin1, Chieh-Wen Cheng, Tsuey-Ching Yang, Shih-Wein Li, Mei-Hsiu Cheng, Lei Wan, Ying-Ju Lin, Chih-Ho Lai, Wei-Yong Lin, Ming-Ching Kao.
Abstract
The interferon (IFN) antagonists of Japanese encephalitis virus (JEV) proteins contribute to the JE pathogenesis. Most flavivirus non-structural (NS) proteins correlate with virus-induced inflammation and immune escape. NS4A proteins of West Nile virus and dengue type 2 virus have been demonstrated to inhibit IFN signaling. In this study, JEV NS4A without the C-terminal 2K domain has been demonstrated to partially block activation of an IFN-stimulated response element (ISRE)-based cis-reporter by IFN-alpha/beta. In addition, JEV NS4A significantly inhibited the phosphorylation levels of STAT1 and STAT2, but not TYK2 in the IFN-treated cells. Moreover, the N-terminus of a RNA helicase DDX42 protein identified using a phage display human brain cDNA library have been demonstrated to specifically bind to JEV NS4A in vitro using a co-immunoprecipitation assay. The interaction between JEV NS4A and RNA helicase DDX42 showed partial co-localization in human medulloblastoma TE-671 cells by confocal microscopy. Importantly, the expression of N-terminal DDX42 is able to overcome JEV-induced antagonism of IFN responses. Therefore, these results show that JEV NS4A without the C-terminal 2K domain is associated with modulation of the IFN response and the interaction of JEV NS4A with RNA helicase DDX42 could be important for JE pathogenesis.Entities:
Mesh:
Substances:
Year: 2008 PMID: 18588927 DOI: 10.1016/j.virusres.2008.05.015
Source DB: PubMed Journal: Virus Res ISSN: 0168-1702 Impact factor: 3.303