Journal of Virology, April 2001, p. 3185-3196, Vol. 75, No. 7
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.7.3185-3196.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Department of Anatomy & Cell Biology, SUNY Downstate Medical Center, Brooklyn, New York 11203,1 and Department of Microbiology & Molecular Genetics, Medical College of Wisconsin, Milwaukee, Wisconsin 532262
Received 18 October 2000/Accepted 8 January 2001
We have analyzed the effects of vaccinia virus (VV) on gamma
interferon (IFN-
) signal transduction. Infection of cells with VV 1 to 2 h prior to treatment with IFN-
inhibits phosphorylation and nuclear translocation of Stat1 and consequently blocks accumulation of mRNAs normally induced by IFN-
. While phosphorylation of other proteins in the IFN-
pathway was not affected, activation of Stat1
by other ligand-receptor systems was also blocked by VV. This block of
Stat1 activation was dose dependent, and although viral protein
synthesis was not required, entry and uncoating of viral cores appear
to be needed to block the accumulation of phosphorylated Stat1. These
results suggest that a virion component is responsible for the effect.
VV virions contain a phosphatase (VH1) that is sensitive to the
phosphatase inhibitor Na3VO4 but not to okadaic
acid. Addition of Na3VO4 but not okadaic acid
restored normal Stat1 phosphorylation levels in VV-infected cells.
Moreover, virions containing reduced levels of VH1 were unable to block the IFN-
signaling pathway. In vitro studies show that the
phosphatase can bind and dephosphorylate Stat1, indicating that this
transcription factor can be a substrate for VH1. Our results reveal a
novel mechanism by which VV interferes with the onset of host immune responses by blocking the IFN-
signal cascade through the
dephosphorylating activity of the viral phosphatase VH1.
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