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Abstract 2016

Rev Esp Quimioter 2016, 29(3):151-154

Identification and in vitro antifungal susceptibility of vaginal Candida spp. isolates to fluconazole, clotrimazole, and nystatin   

                    
MARIA CRISTINA DIAZ, ROSSANNA CAMPONOVO, INGRID ARAYA, ANN CERDA, MARÍA PAOLA SANTANDER, ALFONSO-JAVIER CARRILLO-MUÑOZ             

Objective. The aim of this study was to identify and determine the in vitro antifungal susceptibility testing to clotrimazole, fluconazole, and nystatin of 145 clinical isolates of Candida spp.
Material and methods. M27-A3 microdilution method was used to determine minimal inhibitory concentrations (MIC) and partial MICs (MIC50 and MIC90) of drugs. A total of 145 isolates were studied, 126 were C. albicans, 16 C. glabrata, 2 C. parapsilosis y 1 C. tropicalis.
Results. MIC50 and MIC90 for FLZ against C. albicans were 0.25 mg/L and 1 mg/L respectively and for C. glabrata was achieved at 8 mg/L and 16 mg/L for fluconazole. Five isolates of C. albicans and one isolate of C. tropicalis were in vitro resistant to fluconazole (M27-S4). In C. albicans MIC50 and MIC90 for clotrimazole were of 0.03 mg/L and 0.06 mg/L, respectively. These values for C. glabrata were 0.25 mg/L and 1 mg/L, respectively. Five C. glabrata and 1 C. tropicalis were in vitro resistant to clotrimazole. MIC50 and MIC90 of nystatin were of 1 mg/L and 2 mg/L, respectively for C. albicans and C. glabrata.
Conclusion. In this study, C. albicans is the most frequently isolated yeast, followed by C. glabrata. The antifungals tested were found to be in vitro active for the isolates, except for 6 isolates for fluconazole and 6 to clotrimazole.

Rev Esp Quimioter 2016; 29(3):151-154 [pdf]

12 febrero, 2015/por csanchez
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https://seq.es/wp-content/uploads/2017/10/LOGO-SEQ-800X400.png 0 0 csanchez https://seq.es/wp-content/uploads/2017/10/LOGO-SEQ-800X400.png csanchez2015-02-12 00:00:002015-02-12 00:00:00Rev Esp Quimioter 2016, 29(3):151-154

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Link to: Rev Esp Quimioter 2016, 29(3):151-154 Link to: Rev Esp Quimioter 2016, 29(3):151-154 Rev Esp Quimioter 2016, 29(3):151-154 Link to: Junio 2016, Vol. 29(3): 113-174 Link to: Junio 2016, Vol. 29(3): 113-174 Junio 2016, Vol. 29(3): 113-174
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