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Modification of adherence to plastic and to human buccal cells of <i>Candida albicans</i> and <i>Candida dubliniensis</i> by a subinhibitory concentration of itraconazole
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Citations
14
References
2006
Year
Microbial PathogensFungal Cell BiologyClinical MycologyHost CellDrug ResistanceYeastAntimicrobial ResistanceHealth SciencesAntifungal AgentsFungal PhysiologyAntimicrobial CompoundPharmacologyClinical MicrobiologyFungal PathogenBiologyMycologyHuman Buccal CellsSubinhibitory ConcentrationAntifungal AgentAntibioticsCandida AlbicansPolystyrene Microtiter PlateMicrobiologyAdhesion CapacityMedicine
Exposure to subinhibitory concentrations of antifungal agents can influence the adherence of Candida spp. to the host cell. In this study the adherence of Candida albicans ATCC 10231 and Candida dubliniensis CECT 11455 to plastic and to human buccal epithelial cells was evaluated following pre-exposure to 0.5 x minimum inhibitory capacity (MIC) of itraconazole and compared with the corresponding cellular surface hydrophobicity. The yeasts were grown in Sabouraud broth or RPMI-1640 with itraconazole (0.5 x MIC) for 24-26 h at 37 degrees C and the drug was then removed. The adhesion capacity to plastic was studied by turbidimetry in a polystyrene microtiter plate. The adhesion of the yeast to buccal epithelial cells was determined using microscopy techniques. The cellular surface hydrophobicity levels were determined by the microbial adhesion hydrocarbons test. Pre-exposure to itraconazole decreased plastic adherence and cellular surface hydrophobicity in both species when grown in RPMI. When C. albicans was grown in Sabouraud broth, it was nonhydrophobic and did not adhere and therefore no change was detected with the antibiotic. Itraconazole increased adherence to buccal epithelial cells in both species and media studied, as compared to controls without antifungal agents. To study the effects of these antifungal agents on pathogenicity mechanisms, it will be necessary to standardize the methodology for evaluation to determine their in vivo therapeutic efficacy.
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