Previous Article | Next Article ![]()
Journal of Clinical Microbiology, April 2001, p. 1422-1428, Vol. 39, No. 4
Department of Microbiology and Tumor
Biology
Received 11 September 2000/Returned for modification 29 December
2000/Accepted 26 January 2001
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
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.4.1422-1428.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Fluconazole and Voriconazole Multidisk Testing of
Candida Species for Disk Test Calibration and MIC
Estimation
MTC, Clinical Microbiology, Karolinska Institute,
Karolinska Hospital, Stockholm SE-17176, Sweden
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.
*
Corresponding author. Mailing address: Clinical
Microbiology
MTC, Karolinska Hospital L2:02, Stockholm SE-17176,
Sweden. Phone: 46-8-51774910. Fax: 46-8-308099. E-mail address:
goran.kronvall{at}ks.se.
This article has been cited by other articles:
| Antimicrob. Agents Chemother. | Clin. Microbiol. Rev. |
|---|---|
| Clin. Vaccine Immunol. | ALL ASM JOURNALS |
|---|