Ethanol Enhances the Complete Replication of Hepatitis C Virus: the Role of Acetaldehyde

A method for inhibiting replication of an RNA virus in a cell infected with the virus, wherein the cell is characterized as having been or concurrently being exposed to a physiologically relevant concentration of a compound selected from ethanol, acetate, isopropanol, acetaldehyde or acetone, comprising contacting the cell with an effective amount of an agent selected from atovastatin, cerivastatin, fluvastatin, lovastatin, mevastatin, pitavastatin, pravastatin, rosuvastatin, simastatin, TOFA, cerulenin, thyroxine, bezafibrate, ciprofibrate, clofibrate, gemifibrozil and fenofibrate, thereby inhibiting replication of the virus in the cell.

A method for treating a subject infected with an RNA virus, wherein one or more cells in the subject is characterized as having been or concurrently being exposed to a physiologically relevant concentration of a compound selected from ethanol, acetate, isopropanol, acetaldehyde or acetone, comprising administering to the subject an effective amount of one or more of an HMG-CoA reductase inhibitor, a fatty acid biosynthesis inhibitor, thyroxine or an agent promoting clearance of the compound from a cell, thereby inhibiting replication of the virus in the cell.

A method for treating a subject infected with an RNA virus, wherein one or more cells in the subject are characterized as having been or concurrently being exposed to a physiological concentration of a compound selected from ethanol, acetate, isopropanol, acetaldehyde or acetone, comprising administering to the subject an effective amount of an agent selected from atovastatin, cerivastatin, fluvastatin, lovastatin, mevastatin, pitavastatin, pravastatin, rosuvastatin, simastatin, TOFA, cerulenin, thyroxine, bezafibrate, ciprofibrate, clofibrate, gemifibrozil and fenofibrate, thereby treating the subject.

A method for identifying an agent suitable for inhibiting replication of an RNA virus in a cell infected with the virus, wherein the cell is characterized as having been or concurrently being exposed to a physiologically relevant concentration of a compound selected from ethanol, acetate, isopropanol, acetaldehyde or acetone, comprising contacting a first sample of the cell with a candidate agent and separately contacting a second sample of the cell with contacting the cell with an effective amount of one or more of an HMG-CoA reductase inhibitor mevalonate pathway inhibitor, statins, a fatty acid biosynthesis inhibitor TOFA (5-(Tetradecyloxy)-2-furoic acid), cerulenin, thyroxine to decrease NADH/NAD+ ratio or an agent promoting clearance of the compound from a cell, wherein a decreased replication of the RNA virus in the cell substantially equal to or greater than the decreased replication of the RNA virsus in the second sample of the cell indicates that the candidate agent is suitable for inhibiting replication of the RNA virus in the cell.