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Systemic Candidiasis in Mice: New Insights From an Old Model.

Berit Jungnickel1, Ilse D Jacobsen2,3,4

  • 1Department of Cell Biology, Institute of Biochemistry and Biophysics, Faculty of Biological Sciences, Friedrich Schiller University, Jena, Germany.

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|September 25, 2023
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Summary

Murine models of candidiasis are crucial for antifungal research. New models combining intestinal colonization and systemic infection offer better insights into host-pathogen interactions and immune responses, improving translatability to human patients.

Keywords:
Candida albicansadaptive immunitycolonizationfilamentationmurine infection models

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Area of Science:

  • Mycology and Immunology
  • Infectious Diseases
  • Translational Medicine

Background:

  • Animal models are vital for studying infection pathophysiology, antifungal drug development, and adjunctive therapies.
  • The standard murine model of systemic candidiasis involves intravenous inoculation, which bypasses mucosal barriers.
  • SPF mice lack prior immune exposure to Candida, unlike human patients with established mucosal colonization.

Purpose of the Study:

  • To review findings from mouse models that integrate intestinal colonization with systemic candidiasis.
  • To explore novel insights into host-fungal interactions and immune responses in these advanced models.
  • To discuss the impact of these models on the translatability of research results to human clinical scenarios.

Main Methods:

  • Review of existing literature on murine models of candidiasis.
  • Focus on models incorporating both intestinal colonization and systemic fungal dissemination.
  • Analysis of studies investigating host-pathogen interactions and immune responses in these combined models.

Main Results:

  • Models combining intestinal colonization and systemic infection provide a more realistic simulation of human candidiasis.
  • These advanced models yield novel insights into the complex interplay between the host immune system and Candida.
  • Findings highlight the importance of prior mucosal exposure in shaping the host response to systemic infection.

Conclusions:

  • Mouse models that mimic both colonization and systemic infection are crucial for advancing our understanding of candidiasis.
  • These models enhance the relevance of preclinical findings for human patients.
  • Further research using these models is essential to improve antifungal strategies and patient outcomes.