Ebolavirus VP24 Binding to Karyopherins Is Required for Inhibition of Interferon Signaling

Author:

Mateo Mathieu1234,Reid St. Patrick12345,Leung Lawrence W.5,Basler Christopher F.5,Volchkov Viktor E.1234

Affiliation:

1. Laboratoire des Filovirus, Inserm U758, 21 Av. Tony Garnier, Lyon F-69007, France

2. Université de Lyon, Lyon F-69007, France

3. Université Lyon 1, Villeurbanne F-69622, France

4. IFR 128 BioSciences Gerland-Lyon Sud, Lyon F-69007, France

5. Department of Microbiology, Mount Sinai School of Medicine, New York, New York 10029

Abstract

ABSTRACT The Ebolavirus VP24 protein counteracts alpha/beta interferon (IFN-α/β) and IFN-γ signaling by blocking the nuclear accumulation of tyrosine-phosphorylated STAT1 (PY-STAT1). According to the proposed model, VP24 binding to members of the NPI-1 subfamily of karyopherin alpha (KPNα) nuclear localization signal receptors prevents their binding to PY-STAT1, thereby preventing PY-STAT1 nuclear accumulation. This study now identifies two domains of VP24 required for inhibition of IFN-β-induced gene expression and PY-STAT1 nuclear accumulation. We demonstrate that loss of function correlates with loss of binding to KPNα proteins. Thus, the VP24 IFN antagonist function requires the ability of VP24 to interact with KPNα.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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