PURPOSE: This study examined the effects of cetylpyridinium chloride (CPC) on cell surface hydrophobicity (CSH) and adherence of blastospores of Candida albicans (MEN strain) to human buccal epithelial cells (BEC) in vitro. METHODS: The effect of CPC treatment of either C. albicans blastospores or BEC on their subsequent adherence was determined using 35SO4 labelled blastospores in association with a Percoll gradient. The effects of CPC treatment of blastospores on their CSH was determined using Hydrophobic Interaction Chromatography. RESULTS: Treatment of exponential and stationary phase blastospores with CPC (50 micrograms mL-1) for 0.5-30 minutes, or with CPC (0.5-50 micrograms mL-1) for 15 minutes resulted in significant reductions in both blastospore CSH and adherence to BEC in vitro. No correlation was apparent (r < 0.8) between reduced CSH and reduced blastospore adherence following treatment with CPC (0.5-50 micrograms mL-1). Significantly reduced adherence of C. albicans (stationary or exponential growth phases) to human BEC was also observed following treatment of BEC with CPC (50 micrograms mL-1) for 0.5-30 minutes or with CPC (0.5-50 micrograms mL-1) for 15 minutes. Antiadherence effects were observed at both sub and super-minimum inhibitory concentrations of CPC. CONCLUSIONS: It is suggested that, whilst the ability of CPC to reduce the CSH of C. albicans may contribute to its reduced adherence to human BEC in vitro, reduced CSH is only one of several possible factors that contribute to the observed antiadherence effects.
PURPOSE: This study examined the effects of cetylpyridinium chloride (CPC) on cell surface hydrophobicity (CSH) and adherence of blastospores of Candida albicans (MEN strain) to human buccal epithelial cells (BEC) in vitro. METHODS: The effect of CPC treatment of either C. albicans blastospores or BEC on their subsequent adherence was determined using 35SO4 labelled blastospores in association with a Percoll gradient. The effects of CPC treatment of blastospores on their CSH was determined using Hydrophobic Interaction Chromatography. RESULTS: Treatment of exponential and stationary phase blastospores with CPC (50 micrograms mL-1) for 0.5-30 minutes, or with CPC (0.5-50 micrograms mL-1) for 15 minutes resulted in significant reductions in both blastospore CSH and adherence to BEC in vitro. No correlation was apparent (r < 0.8) between reduced CSH and reduced blastospore adherence following treatment with CPC (0.5-50 micrograms mL-1). Significantly reduced adherence of C. albicans (stationary or exponential growth phases) to human BEC was also observed following treatment of BEC with CPC (50 micrograms mL-1) for 0.5-30 minutes or with CPC (0.5-50 micrograms mL-1) for 15 minutes. Antiadherence effects were observed at both sub and super-minimum inhibitory concentrations of CPC. CONCLUSIONS: It is suggested that, whilst the ability of CPC to reduce the CSH of C. albicans may contribute to its reduced adherence to human BEC in vitro, reduced CSH is only one of several possible factors that contribute to the observed antiadherence effects.
Authors: Nicole O Ponde; Léa Lortal; Gordon Ramage; Julian R Naglik; Jonathan P Richardson Journal: Crit Rev Microbiol Date: 2021-01-22 Impact factor: 7.624
Authors: Dea Shahinas; Anjan Debnath; Christan Benedict; James H McKerrow; Dylan R Pillai Journal: Front Microbiol Date: 2015-04-28 Impact factor: 5.640
Authors: Spyridoula-Angeliki Nikou; Nessim Kichik; Rhys Brown; Nicole O Ponde; Jemima Ho; Julian R Naglik; Jonathan P Richardson Journal: Pathogens Date: 2019-04-22