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Partial reversion of conditional transformation correlates with a decrease in the sensitivity of rat cells to killing

N Salome1, B van Hille, M Geuskens

  • 1Laboratoire d'Oncologie Moléculaire, Institut National de la Santé et de la Recherche Médicale U186, France.

Journal of Virology
|November 1, 1989
PubMed

Insights

Minute virus of mice (MVMp) showed temperature-dependent killing of transformed rat cells. Cell transformation and oncogene expression influence MVMp

Area of Science:

  • Virology
  • Cell Biology
  • Oncology

Background:

  • Minute virus of mice (MVMp) is an autonomous parvovirus.
  • Temperature-sensitive (ts) 339/NRK rat cells exhibit a transformed phenotype regulated by temperature.
  • The v-src oncogene product's role in viral cytopathic effects is not fully understood.

Purpose of the Study:

  • To investigate the cytolytic effect of MVMp on ts 339/NRK rat cells.
  • To determine how temperature-sensitive transformation and oncogene expression affect MVMp-induced cell killing.
  • To explore the relationship between host cell physiology and parvovirus cytopathic effects.

Main Methods:

  • Culturing ts 339/NRK cells with temperature-sensitive transformation.
  • Infecting cells with MVMp at restrictive (39.5°C) and permissive (34.5°C) temperatures.
  • Analyzing viral uptake, replication, particle production, and cytopathic effects using electron microscopy.

Main Results:

  • A shift to permissive temperature significantly increased MVMp-induced cell killing in ts 339/NRK cells.
  • Cells expressing a functional v-src oncogene were sensitive to MVMp at both temperatures.
  • Despite resistance to killing at restrictive temperatures, MVMp replicated efficiently, with virions accumulating in vacuoles.

Conclusions:

  • Host cell transformation and oncogene expression modulate susceptibility to MVMp cytolysis.
  • Reversion to a non-transformed state correlates with non-cytocidal parvovirus production.
  • Cellular physiology influences parvovirus susceptibility by affecting both replication and cytopathic mechanisms.

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