Lipopolysaccharide inhibits virus-mediated induction of interferon genes by disruption of nuclear transport of interferon regulatory factors 3 and 7
We have studied the effects of lipopolysaccharide (LPS) on the Newcastle disease virus (NDV)-mediated induction of cytokine genes expression. Raw cells treated with LPS before or after virus infection showed down-regulation in the expression of interferon A and, to a lesser extent, interferon B gene...
Gespeichert in:
Veröffentlicht in: | The Journal of biological chemistry 1999-06, Vol.274 (25), p.18060-18066 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | We have studied the effects of lipopolysaccharide (LPS) on the Newcastle disease virus (NDV)-mediated induction of cytokine
genes expression. Raw cells treated with LPS before or after virus infection showed down-regulation in the expression of interferon
A and, to a lesser extent, interferon B genes. In contrast, induction of the interleukin (IL)-6 gene was enhanced. The effects
of LPS were not a result of the suppression of virus replication, because the transcription of viral nucleocapsid gene was
not affected. Consistent with these findings, LPS also suppressed the NDV-mediated induction of chloramphenicol acetyltransferase
reporter gene driven by murine interferon A4 promoter in a transient transfection assay. Furthermore, LPS inhibited virus-mediated
phosphorylation of interferon regulatory factor (IRF)-3 and the consequent translocation of IRF-3 from cytoplasm to nucleus.
The LPS-mediated inhibition of IFNA gene expression was much weaker in infected Raw cells that constitutively overexpressed
IRF-3. The nuclear translocation of IRF-7 in infected cells was also inhibited by LPS. These data suggest that LPS down-regulates
the virus-mediated induction of IFNA genes by post-translationally targeting the IRF-3 and IRF-7 proteins. |
---|---|
ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.274.25.18060 |