Abundant defective viral particles budding from microglia in the course of retroviral spongiform encephalopathy

J Virol. 2000 Feb;74(4):1775-80. doi: 10.1128/jvi.74.4.1775-1780.2000.

Abstract

A pathogenetic hallmark of retroviral neurodegeneration is the affinity of neurovirulent retroviruses for microglia cells, while degenerating neurons are excluded from retroviral infections. Microglia isolated ex vivo from rats peripherally infected with a neurovirulent retrovirus released abundant mature type C virions; however, infectivity associated with microglia was very low. In microglia, viral transcription was unaffected but envelope proteins were insufficiently cleaved into mature viral proteins and were not detected on the microglia cell surface. These microglia-specific defects in envelope protein translocation and processing not only may have prevented formation of infectious virus particles but also may have caused further cellular defects in microglia with the consequence of indirect neuronal damage. It is conceivable that similar events play a role in neuro-AIDS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Membrane / metabolism
  • Cells, Cultured
  • Defective Viruses
  • Intracellular Fluid
  • Leukemia Virus, Murine / physiology*
  • Leukemia Virus, Murine / ultrastructure
  • Macrophages, Peritoneal / cytology
  • Macrophages, Peritoneal / virology
  • Mice
  • Microglia / cytology
  • Microglia / ultrastructure
  • Microglia / virology*
  • Protein Processing, Post-Translational
  • Rats
  • Rats, Inbred F344
  • Retroviridae Proteins, Oncogenic / metabolism
  • Transcription, Genetic
  • Viral Envelope Proteins / metabolism
  • Virion

Substances

  • Retroviridae Proteins, Oncogenic
  • Viral Envelope Proteins
  • p15E protein, Murine leukemia virus