Inhibition of dengue virus replication by mycophenolic acid and ribavirin

Author:

Takhampunya Ratree12,Ubol Sukathida1,Houng Huo-Shu3,Cameron Craig E.4,Padmanabhan Radhakrishnan2

Affiliation:

1. Department of Microbiology, Faculty of Science, Mahidol University, 272 Rama VI Road, Bangkok 10400, Thailand

2. Department of Microbiology and Immunology, Georgetown University School of Medicine, 3900 Reservoir Road, Washington, DC 20057, USA

3. Department of Virus Diseases, Walter Reed Army Institute of Research, Silver Spring, MD 20910, USA

4. Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, PA 16802, USA

Abstract

Dengue viruses (DEN), mosquito-borne members of the familyFlaviviridae, are human pathogens of global significance. The effects of mycophenolic acid (MPA) and ribavirin (RBV) on DEN replication in monkey kidney (LLC-MK2) cells were examined. MPA (IC50=0.4±0.3 μM) and RBV (IC50=50.9±18 μM) inhibited DEN2 replication. Quantitative real-time RT-PCR of viral RNA and plaque assays of virions from DEN2-infected and MPA (10 μM)- and RBV (⩾200 μM)-treated cells showed a fivefold increase in defective viral RNA production by cells treated with each drug. Moreover, a dramatic reduction of intracellular viral replicase activity was seen byin vitroreplicase assays. Guanosine reversed the inhibition of these compounds, suggesting that one mode of antiviral action of MPA and RBV is by inhibition of inosine monophosphate dehydrogenase and thereby depletion of the intracellular GTP pool. In addition, RBV may act by competing with guanine-nucleotide precursors in viral RNA translation, replication and 5′ capping.

Publisher

Microbiology Society

Subject

Virology

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