The significance of the difference between two fluorescence frequency distribution histograms (number of fungal cells versus relative fluorescence intensity expressed as arbitrary units on a Palbociclib cost logarithmic scale) was confirmed by statistical analysis using the Kolmogorov-Smirnoff two sample test. The data presented correspond to mean values of the cell surface fluorescence calculated, in all experiments, from the analysis of about 10,000 cells per sample. Microelectrophoresis The PF-02341066 molecular weight net surface charge of the conidia was evaluated with a Zetasizer (Malvern Instruments, Worcestershire, United Kingdom) as described by Uyen et al. [32], by measuring the

electrophoretic mobility of the cells in suspension Etomoxir in distilled water (107 conidia/mL). Data were collected from 5,000 cells, and the zeta potential was calculated for each strain using the Helmotz-Smoluchowski equation. Two-phase partitioning The cell surface hydrophobiCity (CSH) was first determined by two-phase partitioning as described by Kennedy et al. [33] with hexadecane as the hydrocarbon phase. Five hundred microliters of hexadecane were added to 2.5 mL of the conidial suspension (108/mL) in phosphate buffered saline PBS. After vortexing the suspensions (2 min at 2200 vib/min), the tubes were incubated for 10 min at room temperature

to allow the two phases to separate. The absorbance of the aqueous phase was then measured at 630 nm (Dynatech MRX revelation) and compared to that of a control consisting of a conidial suspension treated in the same conditions, but without hexadecane. CSH was also determined using a two-aqueous phase system adapted from Cree et al. [34] and

consisting of a mix 1:1 of a 17.5% dextran 260,000 solution (900 μL) and a 14.26% polyethylene glycol (PEG) 3,350 solution (900 μL) in PBS. Two hundred microliters of the conidial suspension in PBS (107 conidia/mL) were added and the obtained suspensions were gently mixed. The tubes were then incubated for 1 hour at room DNA ligase temperature to allow the two phases to separate. Equal volumes (100 μL) of the upper phase rich in PEG (and therefore considered as hydrophobic) and of the lower phase rich in dextran (and therefore considered as hydrophilic) were then sampled and the absorbance of the two phases measured spectrophotometrically at 630 nm. CSH was expressed as the ratio between the absorbance of the upper phase and that of the lower phase. Transmission electron microscopy The ultrastructure of the conidial wall was investigated by TEM using conidial suspensions obtained from 5-day-old cultures on YPDA as described above. Fixation, post-fixation, dehydratation and embedding in Epon were as previously described [22]. Thin sections contrasted with uranyle acetate and lead citrate were examined on a JEM-2010 transmission electron microscope (Jeol, Paris, France).