Borna disease virus infection of adult and neonatal rats: models for neuropsychiatric disease

Curr Top Microbiol Immunol. 2001:253:157-77. doi: 10.1007/978-3-662-10356-2_8.

Abstract

Animal models provide unique opportunities to explore interactions between host and environment. Two models have been established based on Borna disease virus infection that provide new insights into mechanisms by which neurotropic agents and/or immune factors may impact developing or mature CNS circuitry to effect complex disturbances in movement and behavior. Note in press: Since this chapter was submitted, several manuscripts have been published that extend findings reported here and support the relevance of BDV infections of neonatal Lewis rats as models for investigating mechanisms of neurodevelopmental damage in autism. Behavioral abnormalities, including disturbed play behavior and chronic emotional overactivity, have been described by Pletnikov et al. (1999); inhibition of responses to novel stimuli were described by Hornig et al. (1999); loss of Purkinje cells following neonatal BDV infection has been demonstrated by Eisenman et al. (1999), Hornig et al. (1999), and Weissenböck et al. (2000); and alterations in cytokine gene expression have been reported by Hornig et al. (1999), Plata-Salaman et al. (1999) and Sauder et al. (1999).

MeSH terms

  • Animals
  • Animals, Newborn
  • Apoptosis
  • Borna Disease / physiopathology*
  • Borna Disease / virology
  • Borna disease virus*
  • Brain / growth & development
  • Brain / physiopathology*
  • Brain / virology
  • Cytokines / metabolism
  • Disease Models, Animal
  • Encephalitis, Viral / physiopathology
  • Mental Disorders / physiopathology*
  • Mental Disorders / virology
  • Motor Activity
  • Movement Disorders / physiopathology
  • Movement Disorders / virology
  • Protein Kinase C / metabolism
  • Rats
  • Viral Proteins / metabolism
  • Virus Latency

Substances

  • Cytokines
  • Viral Proteins
  • Protein Kinase C