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Updated: Mar 15, 2026

An Ex vivo Assay to Study Candida albicans Hyphal Morphogenesis in the Gastrointestinal Tract
Published on: July 1, 2020
A functional link between hyphal maintenance and quorum sensing in Candida albicans
Melanie Polke1, Marcel Sprenger2, Kirstin Scherlach3
1Research Group Microbial Immunology, Leibniz Institute for Natural Product Research and Infection Biology, Hans Knoell Institute (HKI), Jena, Germany.
The study identifies the first Candida albicans mutant (eed1Δ) hypersensitive to farnesol, a fungal quorum sensing molecule. This hypersensitivity impacts hyphal development and is linked to altered farnesol production and signaling pathways.
Area of Science:
- Microbiology
- Mycology
- Cell Biology
Background:
- Morphogenesis in Candida albicans, including hyphal development, is regulated by the quorum sensing molecule farnesol.
- The gene EED1 is essential for hyphal extension and maintenance in C. albicans.
Purpose of the Study:
- To investigate the role of EED1 in farnesol sensitivity and signaling.
- To identify the mechanisms underlying farnesol's effects on C. albicans morphogenesis.
Main Methods:
- Deletion mutagenesis to create an eed1Δ strain.
- Construction of hyperactive or deletion mutants for farnesol signaling factors (RAS1, CYR1, CZF1, NRG1).
- Assessment of farnesol sensitivity, production, and effects on filamentation under various conditions, including continuous medium flow.
Main Results:
- The eed1Δ mutant exhibited significantly increased sensitivity to farnesol.
- Farnesol inhibited transient filamentation in eed1Δ cells without causing cell death, suggesting distinct signaling pathways.
- The eed1Δ strain produced higher levels of farnesol, and prolonged filamentation was observed under conditions that reduced farnesol accumulation.
Conclusions:
- EED1 plays a critical role in modulating farnesol sensitivity in Candida albicans.
- Farnesol signaling involves pathways beyond the cAMP cascade.
- There is an intricate link between farnesol sensitivity, production, and the hyphal maintenance defect in the eed1Δ mutant.
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