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Deactivation of macrophage oxidative burst in vitro by different strains of Histoplasma capsulatum

T Ikeda1, J R Little

  • 1Department of Veterinary Microbiology, Azabu University, Kanagawa, Japan.

Mycopathologia
|January 1, 1995
PubMed

Insights

Histoplasma capsulatum yeast deactivates macrophage oxidative burst (OB) in a dose- and time-dependent manner. Virulent Hc strains more effectively induce this deactivation compared to avirulent strains.

Area of Science:

  • Immunology
  • Microbiology
  • Cellular Biology

Background:

  • Histoplasma capsulatum (Hc) yeast is known to evade macrophage immune responses.
  • Previous studies indicated Hc yeast suppresses macrophage oxidative burst (OB) and subsequent stimulation by other agents.

Purpose of the Study:

  • To investigate the dose- and time-dependency of Hc-induced macrophage deactivation.
  • To compare the deactivating potential of virulent versus avirulent Hc strains.
  • To assess the effect of other pathogenic fungi on macrophage OB.

Main Methods:

  • Incubation of murine macrophages with varying concentrations and durations of Hc yeast.
  • Measurement of macrophage oxidative burst (OB) response to Hc yeast and subsequent stimuli (zymosan, PMA).
  • Comparison of deactivation by virulent (G217B) and avirulent (Downs) Hc strains.
  • Assessment of OB stimulation by Candida albicans and Cryptococcus neoformans.

Main Results:

  • Macrophage deactivation by Hc yeast was found to be proportional to incubation time and yeast dose.
  • Virulent Hc strain (G217B) induced a more pronounced deactivation than the avirulent strain.
  • Candida albicans and Cryptococcus neoformans stimulated, rather than deactivated, the macrophage OB.

Conclusions:

  • Histoplasma capsulatum yeast actively suppresses macrophage oxidative burst, a mechanism dependent on dose and duration of exposure.
  • Strain virulence influences the efficacy of Hc-mediated macrophage deactivation.
  • Other pathogenic fungi like Candida albicans and Cryptococcus neoformans exhibit contrasting effects, stimulating macrophage immune activity.

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