Evaluation of a new method for antifungal susceptibility testing for azoles

被引:2
|
作者
Sabra, W. [1 ,2 ]
Tawfik, A. F. [1 ]
Shibl, A. M. [1 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmaceut, Microbiol Unit, Riyadh 11451, Saudi Arabia
[2] Univ Alexandria, Fac Sci, Dept Microbiol, Alexandria, Egypt
来源
WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY | 2010年 / 26卷 / 03期
关键词
Trailing; CLSI broth microdilution method; Azoles; Growth rates; MIC; Candida; CANDIDA-ALBICANS BIOFILMS; CRYPTOCOCCUS-NEOFORMANS; BROTH MICRODILUTION; DRUG-RESISTANCE; IN-VITRO; GROWTH; FLUCONAZOLE; ASPERGILLUS; MICAFUNGIN; RESPONSES;
D O I
10.1007/s11274-009-0188-y
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The interpretation of the end points in azole antifungal drug susceptibility testing is challenging, in part due to incomplete growth inhibition of Candida species. Since the reference Clinical and Laboratory Standards Institute (CLSI) broth microdilution method have limitation with azoles, a new modification of the CLSI microdilution protocol was evaluated. We measure the decrease in growth rate (mu) of exponentially growing cultures in accordance to different azole concentrations at time intervals up to 10 h. Using 15 different Candida strains, an overall agreement within +/- A 2 dilutions by the CLSI method at 24 h in RPMI and the mu-dependent method for three antifungal agents (fluconazole- itraconazole and voriconazole) was achieved. MIC measurement by the new method was less sensitive to the medium used or the inoculum size applied. The presented data suggested that, measuring the in vitro inhibition kinetics at the logarithmic phase could have advantages for addressing susceptibility testing toward azoles.
引用
收藏
页码:451 / 457
页数:7
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