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Isolation of paralysis-inducing murine leukemia viruses from Friend virus passaged in rats

Journal of Virology
|June 1, 1984
PubMed

Insights

Four novel murine leukemia virus clones were isolated from paralyzed rats. Some clones caused paralysis and neurological damage, highlighting viral neurotropism and age-dependent susceptibility in rats.

Area of Science:

  • Virology
  • Neuroscience
  • Oncology

Background:

  • Murine leukemia viruses (MLVs) are retroviruses known to cause various diseases in rodents.
  • Friend leukemia virus (FLV) infection can lead to neurological complications in susceptible hosts.
  • Understanding MLV pathogenesis is crucial for identifying viral factors contributing to disease.

Purpose of the Study:

  • To isolate and characterize novel MLV clones from a paralyzed rat.
  • To investigate the neurovirulence and tropism of these isolated MLV clones.
  • To determine the pathological changes induced by these viruses in the rat central nervous system.

Main Methods:

  • Isolation and propagation of MLV clones (PVC-111, PVC-211, PVC-321, PVC-441) from infected rat tissues.
  • Inoculation of rats with isolated MLV clones to assess paralysis induction and survival rates.
  • Viral growth assessment in brain and spinal cord cell cultures.
  • Immunohistochemical analysis for viral antigen distribution in neural tissues.
  • Histopathological examination of spinal cords for neuronal damage, inflammation, and infiltration.

Main Results:

  • Four MLV clones were isolated; PVC-211, PVC-321, and PVC-441 induced hind leg paralysis and mortality in rats at varying times.
  • PVC-321 and PVC-441 demonstrated efficient replication in brain and spinal cord tissues.
  • Viral antigens were detected predominantly in glial cells, with rare neuronal presence.
  • All MLV clones induced neuronal degeneration in the spinal cord without significant inflammation or leukemic infiltration.
  • Ecotropic and NB-tropic tropism was confirmed for all isolated viruses, with age-dependent susceptibility to paralysis observed.

Conclusions:

  • Specific MLV clones derived from FLV infection exhibit distinct neurovirulence and neurotropism.
  • Glial cells are a primary target for these MLV infections within the central nervous system.
  • The observed neuronal degeneration and age-dependent susceptibility underscore the complex interplay between MLV, host factors, and neurological disease.

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