Functional Portrait of Irf1 (Orf19.217), a Regulator of Morphogenesis and Iron Homeostasis in Candida albicans

Lasse van Wijlick1, Sadri Znaidi1,2, Arturo Hernández-Cervantes1

  • 1Institut Pasteur, Université Paris Cité, INRAE USC2019, Unité Biologie et Pathogénicité Fongiques, Paris, France.

Insights

Candida albicans uses the transcription factor Orf19.217 (Irf1) to form hyphae, crucial for disease. Irf1 regulates iron acquisition and hyphal growth, particularly under iron-deprived conditions, aiding fungal adaptation.

Area of Science:

  • Mycology
  • Molecular Biology
  • Medical Microbiology

Background:

  • Candida albicans exhibits dimorphism, switching between yeast and hyphal forms, which is vital for pathogenesis.
  • The transcription factor Orf19.217 was identified for its role in regulating C. albicans morphology.

Purpose of the Study:

  • To investigate the function of Orf19.217 in C. albicans morphology and iron acquisition.
  • To elucidate the regulatory role of Orf19.217 in fungal adaptation to host environments.

Main Methods:

  • Conditional overexpression and knockout mutant analysis of ORF19.217.
  • Genome-wide expression (RNA-Seq) and location (ChIP-Seq) analyses.
  • Comparative analysis with existing C. albicans hyphal transcriptomes.

Main Results:

  • Orf19.217 (named Irf1) is involved in hyphal morphogenesis and iron acquisition.
  • Irf1-mediated filamentation is distinct from the canonical hyphal program.
  • The orf19.217 mutant is defective in hyphal formation under iron deficiency, but Irf1 overexpression rescues a hap5-mutant defective in iron acquisition.

Conclusions:

  • The transcription factor Irf1 promotes filamentous growth under iron deprivation by stimulating hyphal regulators EFG1 and BRG1.
  • Irf1 is essential for C. albicans adaptation to iron-limited conditions within the human host.
  • Irf1 acts in a parallel pathway to the CCAAT-complex for iron acquisition regulation.