In Vitro Activities of Anidulafungin against More than 2,500 Clinical Isolates of Candida spp., Including 315 Isolates Resistant to Fluconazole
Open accessAbstract
Anidulafungin is an echinocandin antifungal agent with potent activity against Candida spp. We assessed the in vitro activity of anidulafungin against 2,235 clinical isolates of Candida spp. using the CLSI broth microdilution method. Anidulafungin was very active against Candida spp. (the MIC at which 90% of strains are inhibited [MIC(90)] was 2 microg/ml when MIC endpoint criteria of partial inhibition [MIC-2] were used). Candida albicans, C. glabrata, C. tropicalis, C. krusei, and C. kefyr were the most susceptible species of Candida (MIC(90), 0.06 to 0.12 microg/ml), and C. parapsilosis, C. lusitaniae, and C. guilliermondii were the least susceptible (MIC(90), 0.5 to 2 microg/ml). In addition, 315 fluconazole-resistant isolates were tested, and 99% were inhibited by < or =1 microg/ml of anidulafungin. These results provide further evidence for the spectrum and potency of anidulafungin activity against a large and geographically diverse collection of clinically important isolates of Candida spp.
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Triazole-resistant clinical isolates and laboratory strains that demonstrate increased drug efflux pump expression remain susceptible to the echinocandins in laboratory liquid assays.
“Triazole-resistant clinical isolates (Pfaller et al., 2005; Messer et al., 2006) and laboratory strains (Niimi et al., 2006) that demonstrate increased drug efflux pump expression remain susceptible to the echinocandins in laboratory liquid assays.”
From Genetic Drivers of Multidrug Resistance in Candida glabrata (2016) · cites this paper as Pfaller et al., 2005
Interpretive breakpoints for fluconazole, itraconazole, voriconazole, and flucytosine have been developed by considering data relating MICs to known resistance mechanisms, MIC distribution profiles, pharmacokinetic and pharmacodynamic parameters, and the relationship between in vitro activity and clinical outcomes.
“Interpretive breakpoints for four systemically active antifungal agents (fluconazole, itraconazole, voriconazole, and flucytosine [5FC]) have been developed”
From Epidemiology of Invasive Candidiasis: a Persistent Public Health Problem (2007) · cites this paper as [225]
These CLSI methods are reproducible and accurate and provide clinically useful information comparable to that of antibacterial testing.
“These methods are reproducible and accurate and provide clinically useful information that is comparable to that of antibacterial testing (223, 225, 226, 253).”
From Epidemiology of Invasive Candidiasis: a Persistent Public Health Problem (2007) · cites this paper as [225]
In vitro cross-resistance to voriconazole is distinctly uncommon with C. krusei, in contrast to C. glabrata.
“In contrast to C. glabrata , however, in vitro cross-resistance to voriconazole is distinctly uncommon with C. krusei (225)”
From Epidemiology of Invasive Candidiasis: a Persistent Public Health Problem (2007) · cites this paper as [225]
The in vitro activity of voriconazole translates into clinical success in patients infected with C. krusei.
“It also appears that the in vitro activity of voriconazole translates into clinical success in patients infected with C. krusei (123, 182, 225).”
From Epidemiology of Invasive Candidiasis: a Persistent Public Health Problem (2007) · cites this paper as [225]
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- Authors
- Pfaller, M. A., Boyken, L., Hollis, R. J., Messer, S. A., Tendolkar, S., & Diekema, D. J.
- Affiliations
- Departments of Pathology
- University of Iowa (US)
- Corresponding author
- Pfaller, M. A.
- Venue
- Journal of Clinical Microbiology
- Publisher
- American Society for Microbiology
- Published
- 2005-11
- Volume
- 43
- Issue
- 11
- Pages
- 5425-5427
- ISSN
- 0095-1137 (ISSN-L)
- 1098-660X
- PMC
- PMC1287823
- OpenAlex
- W2098505026
- Cited by
- 161
- References
- 19
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 3 · 2023: 3 · 2022: 2 · 2021: 1 · 2020: 1 · 2019: 5 · 2018: 3 · 2017: 5 · 2016: 6 · 2015: 7 · 2014: 4 · 2013: 5 · 2012: 5
- FWCI
- 13.22
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Journal of Clinical Microbiology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Fungal Plant Pathogen Control
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Yeasts and Rust Fungi Studies
- Keywords
- anidulafungin, echinocandins, Candida, antifungal susceptibility, fluconazole resistance, Candida albicans, Candida glabrata, Candida tropicalis, Candida krusei, Candida kefyr, Candida parapsilosis, Candida lusitaniae, Candida guilliermondii, minimum inhibitory concentration, clinical isolates
- MeSH terms
- Anidulafungin, Antifungal Agents, Candida, Candidiasis, Humans, Microbial Sensitivity Tests, Peptides, Cyclic, Fluconazole, Drug Resistance, Fungal, Echinocandins
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