The Host Factor Erlin-1 is Required for Efficient Hepatitis C Virus Infection

Cells. 2019 Dec 2;8(12):1555. doi: 10.3390/cells8121555.

Abstract

Development of hepatitis C virus (HCV) infection cell culture systems has permitted the identification of cellular factors that regulate the HCV life cycle. Some of these cellular factors affect steps in the viral life cycle that are tightly associated with intracellular membranes derived from the endoplasmic reticulum (ER). Here, we describe the discovery of erlin-1 protein as a cellular factor that regulates HCV infection. Erlin-1 is a cholesterol-binding protein located in detergent-resistant membranes within the ER. It is implicated in cholesterol homeostasis and the ER-associated degradation pathway. Silencing of erlin-1 protein expression by siRNA led to decreased infection efficiency characterized by reduction in intracellular RNA accumulation, HCV protein expression and virus production. Mechanistic studies revealed that erlin-1 protein is required early in the infection, downstream of cell entry and primary translation, specifically to initiate RNA replication, and later in the infection to support infectious virus production. This study identifies erlin-1 protein as an important cellular factor regulating HCV infection.

Keywords: HCV; RNA replication; endoplasmic reticulum; erlin-1; erlin-2; hepatitis C virus; host factor; lipid droplet; protein production; virus production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Gene Silencing
  • Hepacivirus / physiology*
  • Hepatitis C / genetics
  • Hepatitis C / metabolism*
  • Hepatitis C / virology*
  • Host-Pathogen Interactions*
  • Humans
  • Lipid Metabolism
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • RNA, Small Interfering / genetics
  • Viral Load
  • Virus Internalization
  • Virus Replication

Substances

  • ERLIN1 protein, human
  • Nerve Tissue Proteins
  • RNA, Small Interfering