Inhibition of Alpha/Beta Interferon Signaling by the NS4B Protein of Flaviviruses

Author:

Muñoz-Jordán Jorge L.1,Laurent-Rolle Maudry1,Ashour Joseph12,Martínez-Sobrido Luis1,Ashok Mundrigi3,Lipkin W. Ian3,García-Sastre Adolfo1

Affiliation:

1. Department of Microbiology

2. Microbiology Graduate School Training Program, Mount Sinai School of Medicine, New York, New York 10029

3. Jerome L. and Dawn Greene Infectious Disease Laboratory, Mailman School of Public Health, Columbia University, New York, New York 10032

Abstract

ABSTRACT Flaviviruses are insect-borne, positive-strand RNA viruses that have been disseminated worldwide. Their genome is translated into a polyprotein, which is subsequently cleaved by a combination of viral and host proteases to produce three structural proteins and seven nonstructural proteins. The nonstructural protein NS4B of dengue 2 virus partially blocks activation of STAT1 and interferon-stimulated response element (ISRE) promoters in cells stimulated with interferon (IFN). We have found that this function of NS4B is conserved in West Nile and yellow fever viruses. Deletion analysis shows that that the first 125 amino acids of dengue virus NS4B are sufficient for inhibition of alpha/beta IFN (IFN-α/β) signaling. The cleavable signal peptide at the N terminus of NS4B, a peptide with a molecular weight of 2,000, is required for IFN antagonism but can be replaced by an unrelated signal peptide. Coexpression of dengue virus NS4A and NS4B together results in enhanced inhibition of ISRE promoter activation in response to IFN-α/β. In contrast, expression of the precursor NS4A/B fusion protein does not cause an inhibition of IFN signaling unless this product is cleaved by the viral peptidase NS2B/NS3, indicating that proper viral polyprotein processing is required for anti-interferon function.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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