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Journal of Virology, June 2000, p. 4957-4966, Vol. 74, No. 11
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Modulation of Dengue Virus Infection in Human Cells
by Alpha, Beta, and Gamma Interferons
Michael S.
Diamond,1,2
T. Guy
Roberts,1
Dianna
Edgil,1
Betty
Lu,1
Joel
Ernst,2,3 and
Eva
Harris1,*
Division of Infectious Diseases, School of
Public Health, University of California, Berkeley, California
947201; Division of Infectious
Diseases, Department of Medicine, University of California, San
Francisco, California 941432; and
Division of Infectious Diseases, Department of Medicine,
San Francisco General Hospital, San Francisco, California
941103
Received 29 December 1999/Accepted 29 February 2000
A role for interferon (IFN) in modulating infection by dengue virus
(DV) has been suggested by studies in DV-infected patients and IFN
receptor-deficient mice. To address how IFN modulates DV type 2 infection, we have assayed IFN-
, -
, and -
for the ability to
enhance or diminish antibody-independent and antibody-dependent cell
infection using a competitive, asymmetric reverse
transcriptase-mediated PCR (RT-PCR) assay that quantitates positive and
negative strands of viral RNA, a flow cytometric assay that measures
viral antigen, and a plaque assay that analyzes virion
production. Our data suggest that IFN-
and -
protect cells
against DV infection in vitro. Treatment of hepatoma cells with IFN-
or -
decreases viral RNA levels greater than 1,000-fold, the
percentage of cells infected 90 to 95%, and the amount of infectious
virus secreted 150- to 100,000-fold. These results have been reproduced
with several cell types and viral strains, including low-passage
isolates. In contrast, IFN-
has a more variable effect depending on
the cell type and pathway of infection. Quantitative RT-PCR
experiments indicate that IFN inhibits DV infection by preventing the
accumulation of negative-strand viral RNA.
*
Corresponding author. Mailing address: School of Public
Health, 140 Warren Hall, University of California, Berkeley, Berkeley, CA 94720. Phone: (510) 642-4845. Fax: (510) 642-6350. E-mail: eharris{at}socrates.berkeley.edu.
Journal of Virology, June 2000, p. 4957-4966, Vol. 74, No. 11
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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