1. Academic Validation
  2. Identification of cell surface molecules involved in dystroglycan-independent Lassa virus cell entry

Identification of cell surface molecules involved in dystroglycan-independent Lassa virus cell entry

  • J Virol. 2012 Feb;86(4):2067-78. doi: 10.1128/JVI.06451-11.
Masayuki Shimojima 1 Ute Ströher Hideki Ebihara Heinz Feldmann Yoshihiro Kawaoka
Affiliations

Affiliation

  • 1 Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan. shimoji-@yamaguchi-u.ac.jp
Abstract

Although O-mannosylated dystroglycan is a receptor for Lassa virus, a causative agent of Lassa fever, recent findings suggest the existence of an alternative receptor(s). Here we identified four molecules as receptors for Lassa virus: Axl and TYRO3, from the TAM family, and dendritic cell-specific intercellular adhesion molecule 3-grabbing nonintegrin (DC-SIGN) and liver and lymph node sinusoidal endothelial calcium-dependent lectin (LSECtin), from the C-type lectin family. These molecules enhanced the binding of Lassa virus to cells and mediated Infection independently of dystroglycan. Axl- or Tyro3-mediated Infection required intracellular signaling via the tyrosine kinase activity of Axl or TYRO3, whereas DC-SIGN- or LSECtin-mediated Infection and binding were dependent on a specific carbohydrate and on ions. The identification of these four molecules as Lassa virus receptors advances our understanding of Lassa virus cell entry.

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