Evaluation of the Etest method for determining voriconazole susceptibilities of 312 clinical isolates of Candida species by using three different agar media
Ma. Pfaller et al., Evaluation of the Etest method for determining voriconazole susceptibilities of 312 clinical isolates of Candida species by using three different agar media, J CLIN MICR, 38(10), 2000, pp. 3715-3717
Performance of the Etest for voriconazole susceptibility testing of 312 iso
lates of Candida spp, was assessed against that of the National Committee f
or Clinical Laboratory Standards (NCCLS) microdilution broth method. The NC
CLS method employed RPMI 1640 broth medium, and MICs were read after incuba
tion for 48 h at 35 degrees C, Etest MICs were determined with RPMI agar co
ntaining 2% glucose (RPG), Casitone agar (CAS), and antibiotic medium 3 (AM
3) agar and were read after incubation for 48 h at 35 degrees C. The Candid
a spp, isolates included C, albicans (n = 174), C. glabrata (n = 55), C. tr
opicalis (n = 31), C. parapsilosis (n = 39), C. krusei (n = 5), C, lusitani
ae (n = 2), and C. guilliermondii (n = 6). The Etest results obtained using
RPG correlated well with the reference MICs, Overall agreement ranged from
91% for C. glabrata to 100% for C. tropicalis, C. parapsilosis, C. guillie
rmondii, C. krusei, and C, lusitaniae, When CAS was used, agreement ranged
from 80% for C, krusei to 100% for C, pampsilosis, C. guilliermondii, and C
. lusitaniae, With AM3, agreement ranged from 58% for C, glabrata to 100% f
or C. lusitaniae and C, guilliermondii. The Etest method using RPG appears
to be a useful method for determining voriconazole susceptibilities of Cand
ida species.