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1.
Rev. Soc. Bras. Med. Trop ; 50(1): 75-79, Jan.-Feb. 2017. tab
Article Dans Anglais | LILACS | ID: biblio-842827

Résumé

ABSTRACT INTRODUCTION: This study evaluated the susceptibilities of oral candidiasis-derived Candida albicans, fluconazole-resistant (FR) Candida dubliniensis, and fluconazole-susceptible (FS) C. dubliniensis to synthetic antiseptics [chlorhexidine gluconate (CHX), cetylpyridinium chloride (CPC), and triclosan (TRC)] and natural compounds (carvacrol, eugenol and thymol). METHODS: Susceptibility tests were performed based on the M27-A3 reference method. The fluconazole-resistant C. dubliniensis strains were obtained after prolonged in vitro exposure to increasing fluconazole concentrations. The geometric mean values for minimum inhibitory concentrations and minimum fungicidal concentrations were compared among the groups. RESULTS: Fluconazole-susceptible C. dubliniensis was more sensitive to CPC and TRC than FR C. dubliniensis and C. albicans were. However, eugenol and thymol were more active against FR C. dubliniensis. The fungicidal activities of CHX and TRC were similar for the three groups, and FR C. dubliniensis and C. albicans had similar sensitivities to CPC. CONCLUSIONS: The resistance of C. dubliniensis to fluconazole affects its sensitivity the synthetic antiseptics and natural compounds that were tested.


Sujets)
Humains , Candida/effets des médicaments et des substances chimiques , Fluconazole/pharmacologie , Anti-infectieux locaux/pharmacologie , Antifongiques/pharmacologie , Thymol/pharmacologie , Triclosan/pharmacologie , Candida/isolement et purification , Candida/classification , Candida albicans/effets des médicaments et des substances chimiques , Eugénol/pharmacologie , Tests de sensibilité microbienne , Cétylpyridinium/pharmacologie , Chlorhexidine/pharmacologie
2.
Mem. Inst. Oswaldo Cruz ; 107(3): 433-436, May 2012. tab
Article Dans Anglais | LILACS | ID: lil-624029

Résumé

The extensive use of azole antifungal agents has promoted the resistance of Candida spp to these drugs. Candida glabrata is a problematic yeast because it presents a high degree of primary or secondary resistance to fluconazole. In Brazil, C. glabrata has been less studied than other species. In this paper, we compared the activity of three major classes of antifungal agents (azoles, echinocandins and polyenes) against fluconazole-susceptible (FS) and fluconazole-resistant (FR) C. glabrata strains. Cross-resistance between fluconazole and voriconazole was remarkable. Among the antifungal agents, the echinocandins were the most effective against FS and FR C. glabrata and micafungin showed the lowest minimal inhibitory concentrations.


Sujets)
Humains , Amphotéricine B/pharmacologie , Antifongiques/pharmacologie , Candida glabrata/effets des médicaments et des substances chimiques , Échinocandines/pharmacologie , Fluconazole/pharmacologie , Pyrimidines/pharmacologie , Triazoles/pharmacologie , Candida glabrata/isolement et purification , Résistance des champignons aux médicaments/effets des médicaments et des substances chimiques , Lipopeptides/pharmacologie , Tests de sensibilité microbienne
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