Utilization of DC-SIGN for entry of feline coronaviruses into host cells

J Virol. 2008 Dec;82(23):11992-6. doi: 10.1128/JVI.01094-08. Epub 2008 Sep 17.

Abstract

The entry and dissemination of viruses in several families can be mediated by C-type lectins such as DC-SIGN. We showed that entry of the serotype II feline coronavirus strains feline infectious peritonitis virus (FIPV) WSU 79-1146 and DF2 into nonpermissive mouse 3T3 cells can be rescued by the expression of human DC-SIGN (hDC-SIGN) and that infection of a permissive feline cell line (Crandall-Reese feline kidney) was markedly enhanced by the overexpression of hDC-SIGN. Treatment with mannan considerably reduced infection of feline monocyte-derived cells expressing DC-SIGN, indicating a role for FIPV infection in vivo.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • CD13 Antigens / physiology
  • Cats
  • Cell Adhesion Molecules / physiology*
  • Coronavirus, Feline / physiology*
  • Humans
  • Lectins, C-Type / physiology*
  • Mannans / pharmacology
  • Mice
  • Receptors, Cell Surface / physiology*

Substances

  • Cell Adhesion Molecules
  • DC-specific ICAM-3 grabbing nonintegrin
  • Lectins, C-Type
  • Mannans
  • Receptors, Cell Surface
  • CD13 Antigens