Antifungal Susceptibility Testing of Candida Isolates from the Candida Surveillance Study
Open accessAbstract
Candida species are a common cause of nosocomial bloodstream infections. Recent surveillance has shown an increase in the relative proportion of infections caused by Candida glabrata, which has reduced susceptibility to fluconazole. We undertook sentinel surveillance with antifungal susceptibility testing to monitor the trends in the proportions of various Candida species causing invasive disease. Forty-one institutions participated in the Candida Surveillance Study. All isolates were submitted to a central laboratory for identification and susceptibility testing. Susceptibility testing was performed in compliance with CLSI guidelines using a custom, broth dilution, microtiter system. There were 5,900 isolates submitted for identification and antifungal susceptibility testing. The distribution of species was as follows: C. albicans, 2,567 (43.5%) isolates; C. glabrata, 1,464 (24.8%) isolates; C. parapsilosis, 1,048 (17.8%) isolates; C. tropicalis, 527 (8.9%) isolates; C. krusei, 109 (1.9%) isolates; C. lusitaniae, 76 (1.3%) isolates; and other Candida species, 109 (1.9%) isolates. Resistance to fluconazole occurred in 1.2% of C. albicans isolates, 5.9% of C. glabrata isolates, 0.3% of C. parapsilosis isolates, and 0.4% of C. tropicalis isolates. Resistance to fluconazole was highly predictive of resistance to voriconazole. Resistance to echinocandins was rarely found, occurring in only 0.2% of all isolates. The rate of fluconazole susceptibility increased significantly from 87.5% in 2005 to 97.4% in 2007. The proportion of cases of disease caused by various Candida species did not change appreciably between 2004 and 2007, and the rate of antifungal susceptibility was high.
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With respect to CLSI clinical breakpoints, fluconazole resistance, defined as MIC values ≥8 mg/L for C. albicans, has been reported overall to be as high as 3.5%.
“With respect to CLSI clinical breakpoints, fluconazole resistance, defined as MIC values ≥8 mg/L for C. albicans, has been reported overall to be as high as 3.5%.43–48”
From Molecular and genetic basis of azole antifungal resistance in the opportunistic pathogenic fungus<i>Candida albicans</i> (2020) · cites this paper as [44]
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- Authors
- Lyon, G. M., Karatela, S., Sunay, S., & Adiri, Y.
- Affiliations
- Emory University (US)
- Venue
- Journal of Clinical Microbiology
- Publisher
- American Society for Microbiology
- Published
- 2010-04
- Volume
- 48
- Issue
- 4
- Pages
- 1270-1275
- ISSN
- 0095-1137 (ISSN-L)
- 1098-660X
- PMC
- PMC2849617
- OpenAlex
- W2117828731
- Cited by
- 111
- References
- 24
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 7 · 2023: 6 · 2022: 6 · 2021: 8 · 2020: 12 · 2019: 10 · 2018: 6 · 2017: 2 · 2016: 8 · 2015: 5 · 2014: 7 · 2013: 13 · 2012: 7
- FWCI
- 5.58
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Clinical Microbiology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Department of Veterans Affairs
- Cleveland Clinic
- University of Washington
- University of Pittsburgh
- University of Louisville
- University of Oklahoma
- University of Rochester
- Hennepin County Medical Center
- Ochsner Health
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Yeasts and Rust Fungi Studies
- Health Sciences › Medicine › Epidemiology › Fungal Infections and Studies
- Keywords
- Candida, antifungal susceptibility, Candida glabrata, fluconazole resistance, voriconazole resistance, echinocandin resistance, Candida albicans, Candida parapsilosis, Candida tropicalis, Candida krusei, Candida lusitaniae, invasive candidiasis, nosocomial bloodstream infection, sentinel surveillance, Candida species distribution
- MeSH terms
- Antifungal Agents, Candida, Candidiasis, Cross Infection, Humans, Microbial Sensitivity Tests, Pyrimidines, Triazoles, Fluconazole, Echinocandins, Voriconazole
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