0625-1024 C188-9 chemical structure μg/ml [40, 41]. Untreated cells served as negative controls. Four replicates were included in

each experiment. The effects of the anti-fungals on planktonic cells were measured by colony counts on Sabouraud agar plates (CFU), or by the XTT and qRT-PCR assays as described above. Biofilm testing To compare the ability of the two assays to quantify changes in mature biofilms stemming from biomass reduction, organisms were grown in 12 well plates for 48 h and their biomass was physically reduced by removing 50%, 33% or 25% of the biofilm from the well surface. To perform this, the round surface area of each well was divided into two, three or four equal parts, and removal of the biofilm from 1/2, 1/3 or 1/4 of the surface area was accomplished with the help of a modified rubber policeman, with a sweeping edge cut to the size of the well radius. Remaining biofilm cells observed microscopically were removed using Belinostat concentration a sterile glass suction tip. XTT and real-time RT-PCR measurements in residual biofilms in these wells were subsequently compared to intact biofilms. To compare the ability of the two assays to quantify changes in viable biofilms in response to different stressors, biofilms grown on plastic were exposed

to pharmacologic [amphotericin B (AMB), 4 μg/ml, 4 h], environmental (100°C, 1 h) or immune cell stressors and viability was measured by the XTT or qRT-PCR assays. To quantify susceptibility to immune cell-inflicted damage we used a neutrophil-like cell line (HL-60, ATCC), as previously described [7]. Briefly, pre-activated HL-60 cells (1.25% DMSO for 7-9 days) were added to biofilms at varying effector to target cell ratios, based on seeding cell densities. After incubation at 37°C,

5% CO2 for 2 hours, media were Selleckchem Semaxanib aspirated, HL-60 cells were lysed with sterile H2O, and fungal viability was assessed with the XTT or qRT-PCR assays. Biofilms grown on mucosal tissues were exposed to anti-fungal drugs (4 μg/ml amphotericin B, 70 μg/ml fluconazole or 8 μg/ml caspofungin [40, 41]) or HL-60 cells for 24 hours, followed by Prostatic acid phosphatase mammalian cell lysis with sterile water. This was followed by the XTT or qRT-PCR assays. Anti-biofilm activity was calculated according to the following formula: % fungal damage = (1-x/n)*100, where × is the OD450 or EFB1 transcript copy number of experimental wells (C. albicans with stressors/effectors) and n is the OD450 or EFB1 transcript copy number of control wells (C. albicans only). All experiments were performed in triplicate. Acknowledgements This study was supported by NIH/NIDCR grant R01 DE13986 to ADB and in part by a General Clinical Research Center grant from NIH (M01RR06192) awarded to the University of Connecticut Health Center, Farmington, CT. References 1.