Establishment and preliminary characterization of a cell line persistently infected with Newcastle disease virus

Acta Pathologica, Microbiologica, Et Immunologica Scandinavica. Section B, Microbiology
|December 1, 1983
PubMed

Insights

Newcastle disease virus (NDV) persistently infected murine osteosarcoma cells, showing reduced growth and viral sensitivity. These OGS-NDV cells exhibited significantly decreased interferon sensitivity, impacting antiviral and cell growth inhibition.

Area of Science:

  • Virology
  • Oncology
  • Immunology

Background:

  • Osteosarcoma is a primary bone cancer.
  • Newcastle disease virus (NDV) is an avian paramyxovirus with oncolytic potential.
  • Persistent viral infections can alter host cell characteristics.

Purpose of the Study:

  • To establish and characterize a murine osteosarcoma (OGS) cell line persistently infected with Newcastle disease virus (NDV).
  • To investigate the biological and immunological consequences of persistent NDV infection in OGS cells.

Main Methods:

  • Permanent infection of OGS cells with NDV.
  • Confirmation of NDV presence using haemadsorption and immunofluorescence assays.
  • Assessment of cell growth rates.
  • Evaluation of OGS-NDV cell sensitivity to various viruses and interferon treatments.

Main Results:

  • NDV was successfully established in OGS cells across multiple passages.
  • Persistently infected OGS-NDV cells displayed a slightly reduced growth rate compared to uninfected OGS cells.
  • OGS-NDV cells demonstrated reduced sensitivity to superinfection by several viruses.
  • A significant reduction in interferon sensitivity was observed in OGS-NDV cells, affecting both antiviral and cell multiplication inhibitory activities.

Conclusions:

  • Persistent NDV infection confers resistance to viral superinfection and modulates cellular responses to interferon in osteosarcoma cells.
  • These findings suggest that NDV-infected osteosarcoma cells exhibit altered biological properties that may have implications for viral oncolysis and host-pathogen interactions.