All samples were tested twice. The data are expressed as mean±SD. The expression of CR3-RP was evaluated by ELISA. The mature biofilm was developed in 96-well polystyrene plates (Sarstedt) according to the protocol of Li et al. (2003). The wells were then washed three times with 1 × PBS and unspecified epitopes were blocked with 100 μL of 1% gelatin as described previously. After a single-step

washing with PBS–0.05% Tween 20, wells were coated with 100 μL (per well) of the anti-CR3-RP antibody (1 : 100 in 1 × PBS) or OKM1 mAb (1 : 10 in 1 × PBS) mAb or control antibody TIB111 (1 : 10 in 1 × PBS) and incubated for 1 h in ice. After three washing steps with PBS–0.05% v/v Tween 20, goat anti-rabbit (for the polyclonal anti-CR3-RP antibody) or goat anti-mouse IgG (for the OKM1 and TIB111 Small molecule library in vivo mAb) conjugated with alkaline phosphatase was added in a final dilution of 1 : 30 000 and the plates were incubated for 1 h at room temperature.

After four additional washing steps, an alkaline phosphatase substrate containing p-nitrophenylphosphate (pNPP, Sigma-Aldrich) was used for development. The reaction was stopped with 3 M NaOH and evaluated at 405 nm using a microplate reader (MRX™, Dynex, Chantilly, VA). The experiment was repeated twice with five parallel wells for every antibody. Final results were calculated as mean±SD. A kinetic of adhesion was performed in polystyrene 24-well plates (Sarstedt) with five selected time points (0, 30, 60, 120, 240 min), according to the protocol of Sohn et al. (2006) with some modifications. Briefly, the loop of 48-culture of yeasts grown on Sabouraud learn more dextrose agar (Biomark Laboratories, Pune, India) was inoculated in 20 mL of YNB medium with amino acids and incubated overnight at 28 °C with shaking. The inoculum was diluted to 0.2 (OD570 nm) in 20 mL of fresh YNB medium. After the subsequent 4-h cultivation at 30 °C with shaking, the density of cell was adjusted to OD570 nm 1 and then diluted 1 : 50 000.

YNB medium (250 μL) and 50 μL of diluted strains was added per well and incubated at 37 °C. After every time point as well as at the starting point (time 0), planktonic cells in 300 μL of YNB medium were inoculated Molecular motor on Petri dishes (diameter 10 cm) with 20 mL yeast–peptone–dextrose (YPD) agar. Wells were then washed once with 1 × PBS, followed by scraping the adherent cells in 300 μL of PBS and inoculating on YPD agar medium. The cultivation of both adherent and nonadherent cells was performed at 28 °C for 48 h. The percentage of adherent cells was calculated in terms of CFU according to the formula: [(adherent cells)/(adherent cells+nonadherent cells)] × 100 for each time point. The experiment was performed in two independent biological replicas and in duplicates for each strain. The results were expressed as mean±SD. This experiment was performed based on the protocol according to Li et al. (2003) described above. However, prior this experiment, both C. albicans strains were adjusted to 107 cells mL−1.