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Use of In Vivo Imaging to Screen for Morphogenesis Phenotypes in Candida albicans Mutant Strains During Active Infection in a Mammalian Host
Published on: October 12, 2022
Two distinct lipid transporters together regulate invasive filamentous growth in the human fungal pathogen Candida
Miguel A Basante-Bedoya1, Stéphanie Bogliolo1, Rocio Garcia-Rodas1,2
1Université Côte d'Azur, CNRS, INSERM, iBV, Parc Valrose, Nice, FRANCE.
Abstract:
Flippases transport lipids across the membrane bilayer to generate and maintain asymmetry. The human fungal pathogen Candida albicans has 5 flippases, including Drs2, which is critical for filamentous growth and phosphatidylserine (PS) distribution. Furthermore, a drs2 deletion mutant is hypersensitive to the antifungal drug fluconazole and copper ions. We show here that such a flippase mutant also has an altered distribution of phosphatidylinositol 4-phosphate [PI(4)P] and ergosterol. Analyses of additional lipid transporters, i.e. the flippases Dnf1-3, and all the oxysterol binding protein (Osh) family lipid transfer proteins, i.e. Osh2-4 and Osh7, indicate that they are not critical for filamentous growth. However, deletion of Osh4 alone, which exchanges PI(4)P for sterol, in a drs2 mutant can bypass the requirement for this flippase in invasive filamentous growth. In addition, deletion of the lipid phosphatase Sac1, which dephosphorylates PI(4)P, in a drs2 mutant results in a synthetic growth defect, suggesting that Drs2 and Sac1 function in parallel pathways. Together, our results indicate that a balance between the activities of two putative lipid transporters regulates invasive filamentous growth, via PI(4)P. In contrast, deletion of OSH4 in drs2 does not restore growth on fluconazole, nor on papuamide A, a toxin that binds PS in the outer leaflet of the plasma membrane, suggesting that Drs2 has additional role(s) in plasma membrane organization, independent of Osh4. As we show that C. albicans Drs2 localizes to different structures, including the Spitzenkörper, we investigated if a specific localization of Drs2 is critical for different functions, using a synthetic physical interaction approach to restrict/stabilize Drs2 at the Spitzenkörper. Our results suggest that the localization of Drs2 at the plasma membrane is critical for C. albicans growth on fluconazole and papuamide A, but not for invasive filamentous growth.
Insights
Flippase Drs2 in Candida albicans is crucial for filamentous growth and membrane organization. Its function in regulating phosphatidylinositol 4-phosphate (PI(4)P) is key, but Drs2 also has roles independent of PI(4)P.
Area of Science:
- Cell Biology
- Mycology
- Biochemistry
Background:
- Flippases are essential membrane proteins that maintain lipid asymmetry.
- In Candida albicans, flippase Drs2 is vital for filamentous growth and phosphatidylserine (PS) distribution.
- Drs2 deletion mutants exhibit hypersensitivity to fluconazole and copper ions.
Purpose of the Study:
- To investigate the roles of Drs2 and other lipid transporters in Candida albicans.
- To elucidate the molecular mechanisms underlying Drs2 function in filamentous growth and drug sensitivity.
- To determine the importance of Drs2 localization for its various functions.
Main Methods:
- Analysis of flippase (Drs2, Dnf1-3) and oxysterol-binding protein (Osh2-4, Osh7) mutants.
- Investigating the effects of Osh4 and Sac1 deletions in a drs2 mutant background.
- Utilizing a synthetic physical interaction approach to manipulate Drs2 localization.
Main Results:
- Drs2 deletion alters phosphatidylinositol 4-phosphate [PI(4)P] and ergosterol distribution.
- Osh4 deletion in a drs2 mutant bypasses the need for Drs2 in invasive filamentous growth.
- Drs2 and Sac1 function in parallel pathways regulating filamentous growth via PI(4)P.
- Drs2 localization at the plasma membrane is critical for growth on fluconazole and papuamide A.
Conclusions:
- A balance between lipid transporters, particularly involving PI(4)P, regulates invasive filamentous growth in C. albicans.
- Drs2 possesses functions beyond PI(4)P regulation, crucial for plasma membrane organization and drug resistance.
- Specific localization of Drs2 at the plasma membrane is essential for antifungal drug efficacy and resistance to toxins.
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