Measles virus persistence in an immortalized murine macrophage cell line

M B Goldman1, D J Buckthal, S Picciotto

  • 1Department of Medicine, College of Medicine, Pennsylvania State University, Hershey 17033.

Virology
|February 20, 1995
PubMed

Insights

Researchers established a persistent measles virus (MV) infection in murine macrophages (IC-21 cells) without causing cell damage. This model allows for detailed studies on viral immunity and infection dissemination.

Area of Science:

  • Virology
  • Immunology
  • Cell Biology

Background:

  • Measles virus (MV) causes significant global health issues.
  • Understanding persistent viral infections is crucial for developing effective treatments and vaccines.
  • Murine macrophage cell lines offer a valuable model for studying viral pathogenesis.

Purpose of the Study:

  • To establish and characterize a persistent measles virus infection in IC-21 murine macrophage cells.
  • To investigate the viral protein expression and stability in persistently infected cells.
  • To provide a model for studying MV dissemination and immunological responses.

Main Methods:

  • Establishing persistent MV infection in IC-21 cells.
  • Immunofluorescence microscopy, flow cytometry, infectious centers assays, and limiting dilution analysis to confirm infection.
  • SDS-PAGE to analyze viral protein expression (Hemagglutinin and phosphoprotein).

Main Results:

  • Persistent MV infection was established in IC-21 cells without cytopathic effects.
  • Expressed Hemagglutinin (H) and phosphoprotein showed altered migration patterns in SDS-PAGE.
  • Viral protein differences were observed between acute and long-term persistent infections.
  • Six sublines maintained infection for 2 years, with fluctuating or consistent virus expression.

Conclusions:

  • IC-21 cells provide a stable in vitro model for persistent measles virus infection.
  • This model facilitates research into viral dissemination and immunological interactions.
  • The model supports studies on viral immunity using established mouse immunological reagents.

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