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Journal of Clinical Microbiology, October 2009, p. 3323-3325, Vol. 47, No. 10
0095-1137/09/$08.00+0 doi:10.1128/JCM.01155-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Departments of Pathology,1 Medicine, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, Iowa 522422
Received 12 June 2009/ Returned for modification 12 August 2009/ Accepted 18 August 2009
We determined the in vitro activities of anidulafungin, caspofungin, and micafungin against 526 isolates of Aspergillus spp. (64 A. flavus, 391 A. fumigatus, 46 A. niger, and 25 A. terreus isolates) collected from over 60 centers worldwide from 2001 through 2007. Susceptibility testing was performed according to the CLSI M38-A2 method. All three echinocandins—anidulafungin (50% minimum effective concentration [MEC50], 0.007 µg/ml; MEC90, 0.015 µg/ml), caspofungin (MEC50, 0.015 µg/ml; MEC90, 0.03 µg/ml), and micafungin (MEC50, 0.007 µg/ml; MEC90, 0.015 µg/ml)—were very active against Aspergillus spp. More than 99% of all isolates were inhibited by
0.06 µg/ml of all three agents.
Published ahead of print on 26 August 2009.
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