TIM-1 Ubiquitination Mediates Dengue Virus Entry

Cell Rep. 2018 May 8;23(6):1779-1793. doi: 10.1016/j.celrep.2018.04.013.

Abstract

Dengue virus (DENV) is a major human pathogen causing millions of infections yearly. Despite intensive investigations, a DENV receptor that directly participates in virus internalization has not yet been characterized. Here, we report that the phosphatidylserine receptor TIM-1 is an authentic DENV entry receptor that plays an active role in virus endocytosis. Genetic ablation of TIM-1 strongly impaired DENV infection. Total internal reflection fluorescence microscopy analyses of live infected cells show that TIM-1 is mostly confined in clathrin-coated pits and is co-internalized with DENV during viral entry. TIM-1 is ubiquitinated at two lysine residues of its cytoplasmic domain, and this modification is required for DENV endocytosis. Furthermore, STAM-1, a component of the ESCRT-0 complex involved in intracellular trafficking of ubiquitinated cargos, interacts with TIM-1 and is required for DENV infection. Overall, our results show that TIM-1 is the first bona fide receptor identified for DENV.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Amino Acid Sequence
  • Cell Line, Tumor
  • Dengue / virology*
  • Dengue Virus / physiology*
  • Dengue Virus / ultrastructure
  • Endocytosis
  • Endosomal Sorting Complexes Required for Transport / metabolism
  • Gene Deletion
  • Hepatitis A Virus Cellular Receptor 1 / chemistry
  • Hepatitis A Virus Cellular Receptor 1 / genetics
  • Hepatitis A Virus Cellular Receptor 1 / metabolism*
  • Humans
  • Phosphoproteins / metabolism
  • Protein Binding
  • Protein Domains
  • Proteomics
  • Ubiquitination*
  • Virus Internalization*

Substances

  • Adaptor Proteins, Signal Transducing
  • Endosomal Sorting Complexes Required for Transport
  • HAVCR1 protein, human
  • Hepatitis A Virus Cellular Receptor 1
  • Phosphoproteins
  • STAM protein, human