Affiliation:
1. Department of Microbiology and Tumor Biology—MTC, Clinical Microbiology, Karolinska Institute, Karolinska Hospital, Stockholm SE-17176, Sweden
Abstract
ABSTRACT
Fluconazole and voriconazole MICs were determined for 114 clinical
Candida
isolates, including isolates of
Candida albicans, Candida glabrata, Candida krusei, Candida lusitaniae, Candida parapsilosis
, and
Candida tropicalis
. All strains were susceptible to voriconazole, and most strains were also susceptible to fluconazole, with the exception of
C. glabrata
and
C. krusei
, the latter being fully fluconazole resistant. Single-strain regression analysis (SRA) was applied to 54 strains, including American Type Culture Collection reference strains. The regression lines obtained were markedly different for the different
Candida
species. Using an MIC limit of susceptibility to fluconazole of ≤8 μg/ml, according to NCCLS standards, the zone breakpoint for susceptibility for the 25-μg fluconazole disk was calculated to be ≥18 mm for
C. albicans
and ≥22 mm for
C. glabrata
and
C. krusei
. SRA results for voriconazole were used to estimate an optimal disk content according to rational criteria. A 5-μg disk content of voriconazole gave measurable zones for a tentative resistance limit of 4 μg/ml, whereas a 2.5-μg disk gave zones at the same MIC level for only three of the species. A novel SRA modification, multidisk testing, was also applied to the two major species,
C. albicans
and
C. glabrata
, and the MIC estimates were compared with the true MICs for the isolates. There was a significant correlation between the two measurements. Our results show that disk diffusion methods might be useful for azole testing of
Candida
isolates. The method can be calibrated using SRA. Multidisk testing gives direct estimations of the MICs for the isolates.
Publisher
American Society for Microbiology
Cited by
20 articles.
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