Role of IFN-gamma in an experimental murine model of West Nile virus-induced seizures

J Neurochem. 2007 Nov;103(3):1019-30. doi: 10.1111/j.1471-4159.2007.04798.x. Epub 2007 Sep 5.

Abstract

Seizures are a major complication of viral encephalitis. However, the mechanisms of seizure-associated neuronal dysfunction remain poorly understood. We report that intranasal inoculation with West Nile virus (WNV) (Sarafend) causes limbic seizures in C57BL/6 mice, but not in interferon (IFN)-gamma-deficient (IFN-gamma-/-) mice. Both strains showed similar levels of virus in the brain, as well as similar concentrations of the cytokines, tumor necrosis factor and interleukin-6, both of which can alter neuronal excitability. Experiments in chimeric IFN-gamma-/- mice reconstituted with IFN-gamma-producing leukocytes showed that IFN-gamma is not required during central nervous system infection for limbic seizure development, suggesting a role for IFN-gamma in the developing brain. This was supported responses to pentylenetetrazole, kainic acid (KA), and N-methyl-d-aspartate (NMDA). Both strains of mice exhibited similar behavior after pentylenetetrazole challenge. However, while NMDA and KA treatment resulted in characteristic seizures in C57BL/6 mice, these responses were diminished (NMDA treatment) or absent (KA treatment) in IFN-gamma-/- mice. Furthermore, NMDA-receptor blockade with MK-801 in WNV-infected C57BL/6 mice abrogated seizures and prolonged survival. Our data show that IFN-gamma plays an important role in the development of the excitatory seizure pathways in the brain and that these cascades become pathogenic in encephalitic WNV infection.

Publication types

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

MeSH terms

  • Animals
  • Brain / immunology*
  • Brain / physiopathology
  • Brain / virology*
  • Chlorocebus aethiops
  • Convulsants / pharmacology
  • Disease Models, Animal
  • Excitatory Amino Acid Antagonists / pharmacology
  • Female
  • Genetic Predisposition to Disease / genetics
  • Glutamic Acid / metabolism
  • Interferon-gamma / genetics
  • Interferon-gamma / immunology*
  • Interleukin-6 / immunology
  • Interleukin-6 / metabolism
  • Limbic Encephalitis / genetics
  • Limbic Encephalitis / immunology
  • Limbic Encephalitis / virology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Neural Pathways / immunology
  • Neural Pathways / physiopathology
  • Neural Pathways / virology
  • Receptors, N-Methyl-D-Aspartate / agonists
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Seizures / genetics
  • Seizures / immunology*
  • Seizures / virology*
  • Synaptic Transmission / genetics
  • Synaptic Transmission / immunology
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / metabolism
  • Vero Cells
  • West Nile Fever / complications
  • West Nile Fever / immunology*
  • West Nile Fever / physiopathology

Substances

  • Convulsants
  • Excitatory Amino Acid Antagonists
  • Interleukin-6
  • Receptors, N-Methyl-D-Aspartate
  • Tumor Necrosis Factor-alpha
  • Glutamic Acid
  • Interferon-gamma