Induction of inflammation by West Nile virus capsid through the caspase-9 apoptotic pathway

Emerg Infect Dis. 2002 Dec;8(12):1379-84. doi: 10.3201/eid0812.020224.

Abstract

West Nile virus (WNV) is a member of the Flaviviridae family of vector-borne pathogens. Clinical signs of WNV infection include neurologic symptoms, limb weakness, and encephalitis, which can result in paralysis or death. We report that the WNV-capsid by itself induces rapid nuclear condensation and cell death in tissue culture. Apoptosis is induced through the mitochondrial pathway resulting in caspase-9 activation and downstream caspase-3 activation. Capsid gene delivery into the striatum of mouse brain or interskeletal muscle resulted in cell death and inflammation, likely through capsid-induced apoptosis in vivo. These studies demonstrate that the capsid protein of WNV may be responsible for aspects of viral pathogenesis through induction of the apoptotic cascade.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Apoptosis
  • Brain / virology
  • Capsid Proteins / genetics
  • Capsid Proteins / physiology*
  • Caspase 9
  • Caspases / physiology*
  • Female
  • Mice
  • Mice, Inbred BALB C
  • West Nile Fever / etiology
  • West Nile virus / genetics
  • West Nile virus / pathogenicity*

Substances

  • Capsid Proteins
  • Casp9 protein, mouse
  • Caspase 9
  • Caspases