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Journal of Virology, November 2009, p. 11397-11401, Vol. 83, No. 21
0022-538X/09/$08.00+0 doi:10.1128/JVI.00989-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Carlyne D. Cool,3,4,
and
Linda F. van Dyk1,2,
*
Departments of Microbiology,1 Immunology,2 Pathology, University of Colorado Denver, School of Medicine, Aurora, Colorado,3 National Jewish Health, Denver, Colorado4
Received 15 May 2009/ Accepted 19 August 2009
Gamma interferon (IFN-
) is critical for the control of chronic infection with murine gammaherpesvirus 68 (
HV68). Current data indicate that IFN-
has a lesser role in the control of acute replication of
HV68. Here, we show that IFN-
-deficient mice on the BALB/c genetic background poorly control acute viral replication and succumb to early death by acute pneumonia. Notably, this acute, lethal pneumonia was dependent not only on the viral dose, but also on specific viral genes including the viral cyclin gene, previously identified to be important in promoting optimal chronic infection and reactivation from latency.
Published ahead of print on 26 August 2009.
Contributions: K.S.L. performed research; C.D.C. analyzed histological tissues; and K.S.L. and L.F.V.D. designed experiments, interpreted data, and wrote the manuscript.
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