C. albicans SC5314 were grown overnight in YPD medium. And then, 1 × 106 cells/mL with or without compounds were incubated in RPMI 1640 medium, GlcNAc (0.5% GlcNAc, 0.5% peptone, 0.3% KH2PO4) or 10% FBS YPD medium at 37°C for 4 h. Inhibition quantification of the yeast-to-hyphal-form transition was accomplished by counting the number of individual budded cells versus the number of hyphae in the population as previously described [26 (link)]. More than 100 cells were counted for each well in duplicate, and all assays were repeated for five times. Images of cells were obtained using a microscope. The experiments were performed in triplicate.
Quantifying Candida albicans Morphogenesis
C. albicans SC5314 were grown overnight in YPD medium. And then, 1 × 106 cells/mL with or without compounds were incubated in RPMI 1640 medium, GlcNAc (0.5% GlcNAc, 0.5% peptone, 0.3% KH2PO4) or 10% FBS YPD medium at 37°C for 4 h. Inhibition quantification of the yeast-to-hyphal-form transition was accomplished by counting the number of individual budded cells versus the number of hyphae in the population as previously described [26 (link)]. More than 100 cells were counted for each well in duplicate, and all assays were repeated for five times. Images of cells were obtained using a microscope. The experiments were performed in triplicate.
Corresponding Organization : Southeast University
Protocol cited in 8 other protocols
Variable analysis
- Compounds
- Growth medium (RPMI 1640, GlcNAc, or 10% FBS YPD)
- Inhibition of the yeast-to-hyphal-form transition
- Number of individual budded cells vs. hyphae in the population
- Cell density (1 × 10^6 cells/mL)
- Incubation time (4 h)
- Incubation temperature (37°C)
- Cells grown in the respective media without any compounds (negative control)
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