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Changes in cyclic nucleotide levels and dimorphic transition in Candida albicans
Journal of Bacteriology
|June 1, 1980
Summary
Cyclic adenosine monophosphate (cAMP) influences the dimorphic transition in Candida albicans. Increased cAMP levels promote yeast-to-hyphal transition, while cysteine reverses this effect.
Area of Science:
- Mycology
- Molecular Biology
- Cell Biology
Background:
- Candida albicans is a pathogenic fungus that exhibits dimorphism.
- Dimorphic transition is crucial for C. albicans virulence.
- The role of cyclic nucleotides in this transition is not fully understood.
Purpose of the Study:
- To investigate the relationship between cyclic nucleotide levels and dimorphic transition in Candida albicans.
- To determine the specific roles of cyclic adenosine 3',5'-monophosphate (cAMP) and cyclic guanosine 3',5'-monophosphate (cGMP) in fungal morphology.
Main Methods:
- Quantification of intracellular cAMP and cGMP levels in yeast-form C. albicans.
- Induction of germ tube formation at 40°C and assessment of cyclic nucleotide changes.
- Treatment with cysteine to observe effects on germination and cAMP levels.
- Application of dibutyryl cAMP to induce germination in specific media and temperatures.
Main Results:
- Both cAMP and cGMP were detected in yeast-form C. albicans, with cGMP at approximately one-tenth the concentration of cAMP.
- Germ tube formation at 40°C correlated with a significant increase in intracellular cAMP, without altering cGMP levels.
- Cysteine inhibited germination and reversed the rise in intracellular cAMP.
- Exogenous dibutyryl cAMP (1 mM) promoted germination in proline medium at 32-34°C.
Conclusions:
- Intracellular cAMP levels are closely linked to the dimorphic transition in Candida albicans.
- cAMP appears to be a key signaling molecule regulating yeast-to-hyphal morphological changes.
- Modulation of cAMP levels can control germination and potentially influence C. albicans pathogenicity.