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Immunological responses to Candida albicans II. Amyloidosis in mice induced by candidiasis

Infection and Immunity
|December 1, 1974
PubMed

Insights

Candida albicans infection rapidly causes amyloidosis in C57BL/Ks mice. Other mouse strains and yeast species show slower or lesser amyloid induction, indicating strain- and species-specific responses to fungal infections.

Area of Science:

  • Microbiology and Immunology
  • Pathology
  • Host-Pathogen Interactions

Background:

  • Fungal infections, particularly Candida albicans, can trigger host immune responses.
  • Amyloidosis, the abnormal accumulation of proteins, can be influenced by inflammatory processes.
  • Understanding host responses to fungal pathogens is crucial for developing effective treatments.

Purpose of the Study:

  • To investigate the induction of amyloidosis by Candida albicans infection in different mouse strains.
  • To compare the amyloidogenic potential of viable and heat-killed Candida albicans.
  • To assess the amyloid-inducing capacity of Saccharomyces cerevisiae.

Main Methods:

  • Induction of infection in mouse thigh models using viable Candida albicans.
  • Inoculation with viable Saccharomyces cerevisiae and heat-killed Candida albicans.
  • Assessment of amyloid deposition in different mouse strains (C57BL/Ks, C3H, AKR).

Main Results:

  • Rapid and significant amyloidosis was observed in C57BL/Ks mice infected with Candida albicans.
  • Slower and less pronounced amyloid induction occurred in C3H and AKR mice.
  • Both viable Saccharomyces cerevisiae and heat-killed Candida albicans induced amyloidosis in C57BL/Ks mice, though the kinetics and extent may differ.

Conclusions:

  • Candida albicans infection is a potent inducer of amyloidosis in susceptible mouse strains.
  • Host genetic background significantly influences the development of infection-induced amyloidosis.
  • Different fungal species and forms (viable vs. heat-killed) can elicit amyloidogenic responses, highlighting the complexity of host-fungal interactions.

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