Borna disease virus infection impairs synaptic plasticity

J Virol. 2007 Aug;81(16):8833-7. doi: 10.1128/JVI.00612-07. Epub 2007 Jun 6.

Abstract

The mechanisms whereby Borna disease virus (BDV) can impair neuronal function and lead to neurobehavioral disease are not well understood. To analyze the electrophysiological properties of neurons infected with BDV, we used cultures of neurons grown on multielectrode arrays, allowing a real-time monitoring of the electrical activity across the network shaped by synaptic transmission. Although infection did not affect spontaneous neuronal activity, it selectively blocked activity-dependent enhancement of neuronal network activity, one form of synaptic plasticity thought to be important for learning and memory. These findings highlight the original mechanism of the neuronal dysfunction caused by noncytolytic infection with BDV.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Borna Disease / physiopathology*
  • Borna disease virus*
  • Cerebral Cortex / physiopathology*
  • Cerebral Cortex / virology
  • Electrophysiology
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Neuronal Plasticity*
  • Neurons / virology
  • Phosphoproteins / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction
  • Synapses / virology*
  • Synaptic Transmission
  • Viral Structural Proteins / metabolism

Substances

  • P protein, Borna disease virus
  • Phosphoproteins
  • Viral Structural Proteins
  • Extracellular Signal-Regulated MAP Kinases