Antifungal susceptibility of bloodstream yeasts isolated at a public children’s hospital in Brazil: comparison of the Etest® and the AFST–EUCAST microdilution method

Author:

Matsumoto Flávia E.1234,Dias Amanda L.T.1234,Melhem Márcia S.C.1234,Szeszs Maria W.1234,Auler Marcos E.1234,Ruiz Luciana S.1234,Gonçalves da Silva Ériques1234,Gandra Rinaldo F.1234,Paula Claudete R.1234

Affiliation:

1. Departamento de Microbiologia, Laboratório de Micologia, Instituto de Ciências Biomédicas II, Universidade de São Paulo (USP), Av. Prof. Lineu Prestes, 1374 CEP 05508–900, São Paulo-SP, Brazil.

2. Departamento de Ciências Biológicas, Laboratório de Microbiologia, Universidade Federal de Alfenas, MG, Brazil.

3. Instituto Adolfo Lutz, São Paulo-SP, Brazil.

4. Centro de Ciências Médicas e Farmacêuticas, Universidade Estadual do Oeste do Paraná, Cascavel, PR, Brazil.

Abstract

This study compared the minimum inhibitory concentration (MIC) results from the proposed standard methods of the Antifungal Susceptibility Testing Subcommittee of the European Committee on Antibiotic Susceptibility Testing (AFST–EUCAST) with the commercial system Etest® in the evaluation of susceptibility to flucytosine, fluconazole, itraconazole, voriconazole, and amphotericin B of 136 Candida spp. isolated from the blood of hospitalized children. The results presented a greater agreement among Etest® MICs ±2 log2 dilutions of AFST–EUCAST for fluconazole (98.1% and 96.3%) and voriconazole (100% and 100%) for Candida albicans and Candida parapsilosis . For Candida glabrata , the agreement was greater only for fluconazole (81.8%) and voriconazole (100%). For amphotericin B, the agreement between the methods was low for all species. The agreement percentage among the Etest® and AFST–EUCAST susceptibility profiles was high according to the MIC breakpoints recommended by the M27-A2 protocol for the majority of the yeasts, except for fluconazole and itraconazole against Candida tropicalis and for itraconazole against C. glabrata and Candida krusei . According to both methodologies, a great number of Candida spp. isolates showed an in vitro susceptibility to all evaluated antifungal agents. Overall, both procedures can be reliable techniques for susceptibility tests of yeasts, but the assessment of interlaboratory agreement and correlation of MICs by different methods with in vivo response are of great importance.

Publisher

Canadian Science Publishing

Subject

Genetics,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Immunology,Microbiology

Reference24 articles.

1. In Vivo Pharmacokinetics and Pharmacodynamics of a New Triazole, Voriconazole, in a Murine Candidiasis Model

2. Comparison of Etest, microdilution and colorimetric dilution with reference broth macrodilution method for antifungal susceptibility testing of clinically significantCandidaspecies isolated from immunocompromised patients

3. Comparison of Visual and Spectrophotometric Methods of Broth Microdilution MIC End Point Determination and Evaluation of a Sterol Quantitation Method for In Vitro Susceptibility Testing of Fluconazole and Itraconazole against Trailing and Nontrailing Candida Isolates

4. Clinical and Laboratory Standards Institute. 2002. Reference method for broth dilution antifungal susceptibility testing for yeasts; approved standard. 2nd ed. CLSI document M27-A2. Clinical and Laboratory Standards Institute, Wayne, Pa.

5. Clinical and Laboratory Standards Institute. 2005. Quality control minimal inhibitory concentration (MIC) limits for broth microdilution and MIC interpretative breakpoints. CLSI document M27-S2. Clinical and Laboratory Standards Institute, Wayne, Pa.

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