IFITM-2 and IFITM-3 but Not IFITM-1 Restrict Rift Valley Fever Virus

Author:

Mudhasani Rajini1,Tran Julie P.1,Retterer Cary1,Radoshitzky Sheli R.1,Kota Krishna P.1,Altamura Louis A.1,Smith Jeffrey M.1,Packard Beverly Z.2,Kuhn Jens H.3,Costantino Julie1,Garrison Aura R.1,Schmaljohn Connie S.1,Huang I-Chueh4,Farzan Michael5,Bavari Sina1

Affiliation:

1. United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland USA

2. OncoImmunin, Inc., Gaithersburg, Maryland, USA

3. Integrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Fort Detrick, Frederick, Maryland, USA

4. Department of Cell Biology and Neuroscience, University of California Riverside, Riverside, California, USA

5. Department of Microbiology and Molecular Genetics, Harvard Medical School, New England Primate Research Center, Southborough, Massachusetts, USA

Abstract

ABSTRACT We show that interferon-induced transmembrane protein 1 (IFITM-1), IFITM-2, and IFITM-3 exhibit a broad spectrum of antiviral activity against several members of the Bunyaviridae family, including Rift Valley fever virus (RVFV), La Crosse virus, Andes virus, and Hantaan virus, all of which can cause severe disease in humans and animals. We found that RVFV was restricted by IFITM-2 and -3 but not by IFITM-1, whereas the remaining viruses were equally restricted by all IFITMs. Indeed, at low doses of alpha interferon (IFN-α), IFITM-2 and -3 mediated more than half of the antiviral activity of IFN-α against RVFV. IFITM-2 and -3 restricted RVFV infection mostly by preventing virus membrane fusion with endosomes, while they had no effect on virion attachment to cells, endocytosis, or viral replication kinetics. We found that large fractions of IFITM-2 and IFITM-3 occupy vesicular compartments that are distinct from the vesicles coated by IFITM-1. In addition, although overexpression of all IFITMs expanded vesicular and acidified compartments within cells, there were marked phenotypic differences among the vesicular compartments occupied by IFITMs. Collectively, our data provide new insights into the possible mechanisms by which the IFITM family members restrict distinct viruses.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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