Japanese encephalitis virus disrupts cell-cell junctions and affects the epithelial permeability barrier functions

PLoS One. 2013 Jul 24;8(7):e69465. doi: 10.1371/journal.pone.0069465. Print 2013.

Abstract

Japanese encephalitis virus (JEV) is a neurotropic flavivirus, which causes viral encephalitis leading to death in about 20-30% of severely-infected people. Although JEV is known to be a neurotropic virus its replication in non-neuronal cells in peripheral tissues is likely to play a key role in viral dissemination and pathogenesis. We have investigated the effect of JEV infection on cellular junctions in a number of non-neuronal cells. We show that JEV affects the permeability barrier functions in polarized epithelial cells at later stages of infection. The levels of some of the tight and adherens junction proteins were reduced in epithelial and endothelial cells and also in hepatocytes. Despite the induction of antiviral response, barrier disruption was not mediated by secreted factors from the infected cells. Localization of tight junction protein claudin-1 was severely perturbed in JEV-infected cells and claudin-1 partially colocalized with JEV in intracellular compartments and targeted for lysosomal degradation. Expression of JEV-capsid alone significantly affected the permeability barrier functions in these cells. Our results suggest that JEV infection modulates cellular junctions in non-neuronal cells and compromises the permeability barrier of epithelial and endothelial cells which may play a role in viral dissemination in peripheral tissues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Caco-2 Cells
  • Cell Line
  • Claudin-1 / metabolism
  • Encephalitis Virus, Japanese / physiology*
  • Epithelial Cells / metabolism
  • Epithelial Cells / virology
  • Fluorescent Antibody Technique
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Human Umbilical Vein Endothelial Cells / virology
  • Humans
  • Intestinal Mucosa / cytology
  • Reactive Oxygen Species / metabolism
  • Real-Time Polymerase Chain Reaction
  • Virus Replication / physiology

Substances

  • Claudin-1
  • Reactive Oxygen Species

Grants and funding

This study was supported by the institutional grant and by the extra-mural funds from the Department of Biotechnology to GRM (BT/PR5132/MED/15/85/2012). TA is supported by vaccine research innovation award of the institute. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.