USP15 Participates in Hepatitis C Virus Propagation through Regulation of Viral RNA Translation and Lipid Droplet Formation

Author:

Kusakabe Shinji1,Suzuki Tatsuya1,Sugiyama Yukari1,Haga Saori1,Horike Kanako1,Tokunaga Makoto1,Hirano Junki1,Zhang He1,Chen David Virya1,Ishiga Hanako1,Komoda Yasumasa1,Ono Chikako1,Fukuhara Takasuke1,Yamamoto Masahiro2,Ikawa Masahito3,Satoh Takashi4,Akira Shizuo4,Tanaka Tomohisa5,Moriishi Kohji5ORCID,Fukai Moto6,Taketomi Akinobu6,Yoshio Sachiyo7,Kanto Tatsuya7,Suzuki Tetsuro8,Okamoto Toru1,Matsuura Yoshiharu1

Affiliation:

1. Department of Molecular Virology, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan

2. Department of Immunoparasitology, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan

3. Department of Experimental Genome Research, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan

4. Department of Host Defense, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan

5. Department of Microbiology, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan

6. Department of Gastroenterological Surgery I, Hokkaido University Graduate School of Medicine, Sapporo, Japan

7. Research Center for Hepatitis and Immunology, National Center for Global Health and Medicine, Ichikawa, Japan

8. Department of Virology and Parasitology, Hamamatsu University School of Medicine, Hamamatsu, Japan

Abstract

Although ubiquitination has been shown to play important roles in the HCV life cycle, the roles of deubiquitinating enzymes (DUBs), which cleave ubiquitin chains from their substrates, in HCV propagation have not been investigated. Here, we identified USP15 as a DUB regulating HCV propagation. USP15 showed no interaction with viral proteins and no participation in innate immune responses. Deficiency of USP15 in Huh7 cells resulted in suppression of the translation of HCV RNA and reduction in the amounts of lipid droplets, and the addition of fatty acids partially restored the production of infectious HCV particles. These data suggest that USP15 participates in HCV propagation in hepatic cells through the regulation of viral RNA translation and lipid metabolism.

Funder

Japan Agency for Medical Research and Development

Ministry of Education, Culture, Sports, Science and Technology

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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