Experimental measles encephalitis in Lewis rats: dissemination of infected neuronal cell subtypes

Ulrike Jehmlich1, Jennifer Ritzer, Jens Grosche

  • 1Institute of Virology, Leipzig University, Johannisallee 30, 04103, Leipzig, Germany.

Journal of Neurovirology
|September 3, 2013
PubMed

Insights

Subacute sclerosing panencephalitis (SSPE) arises from persistent measles virus (MV) brain infections. This study reveals MV primarily infects specific neuron types in rats, explaining SSPE

Area of Science:

  • Neuroscience
  • Virology
  • Immunology

Background:

  • Subacute sclerosing panencephalitis (SSPE) is a rare, progressive central nervous system disease linked to persistent measles virus (MV) infection.
  • Understanding MV's cellular targets in the brain is crucial for elucidating SSPE pathogenesis.

Purpose of the Study:

  • To identify specific cell populations infected by a neurotropic MV strain in an experimental encephalitis model.
  • To map the distribution of MV within the rat brain to understand its dissemination pathways.

Main Methods:

  • Utilized an experimental encephalitis model in Lewis rats infected with the neurotropic MV strain CAM/RB.
  • Employed multiple immunofluorescence labeling and confocal laser scanning microscopy to detect MV antigen in brain sections.
  • Analyzed MV distribution patterns in relation to specific cell markers, including neuronal subtypes.

Main Results:

  • Measles virus (MV) was detected exclusively in neurons, not in glial cells, endothelial cells, or microglia.
  • MV antigen was present in GABAergic and glutamatergic neurons but absent in cholinergic and catecholaminergic neurons.
  • Infected neurons were predominantly located in the motor, somatosensory, auditory, and visual cortices, as well as the basal ganglia and thalamic nuclei.

Conclusions:

  • Measles virus (MV) appears to disseminate within the brain via GABAergic and glutamatergic neurons and their processes.
  • The restricted viral tropism suggests inefficient immune clearance from infected neurons, correlating with observed disease symptoms in SSPE.

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