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Activity of a Long-Acting Echinocandin, Rezafungin, and Comparator Antifungal Agents Tested against Contemporary Invasive Fungal Isolates (SENTRY Program, 2016 to 2018)

We evaluated the activity of rezafungin and comparators, using Clinical and Laboratory Standards Institute (CLSI) broth microdilution methods, against a worldwide collection of 2,205 invasive fungal isolates recovered from 2016 to 2018. Candida (n = 1,904 isolates; 6 species), Cryptococcus neoforman...

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Autores principales: Pfaller, Michael A., Carvalhaes, Cecilia, Messer, Shawn A., Rhomberg, Paul R., Castanheira, Mariana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179261/
https://www.ncbi.nlm.nih.gov/pubmed/32015043
http://dx.doi.org/10.1128/AAC.00099-20
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author Pfaller, Michael A.
Carvalhaes, Cecilia
Messer, Shawn A.
Rhomberg, Paul R.
Castanheira, Mariana
author_facet Pfaller, Michael A.
Carvalhaes, Cecilia
Messer, Shawn A.
Rhomberg, Paul R.
Castanheira, Mariana
author_sort Pfaller, Michael A.
collection PubMed
description We evaluated the activity of rezafungin and comparators, using Clinical and Laboratory Standards Institute (CLSI) broth microdilution methods, against a worldwide collection of 2,205 invasive fungal isolates recovered from 2016 to 2018. Candida (n = 1,904 isolates; 6 species), Cryptococcus neoformans (n = 73), Aspergillus fumigatus (n = 183), and Aspergillus flavus (n = 45) isolates were tested for their susceptibility (S) to rezafungin as well as the comparators caspofungin, anidulafungin, micafungin, and azoles. Interpretive criteria were applied following CLSI published clinical breakpoints (CBPs) and epidemiological cutoff values (ECVs). Isolates displaying non-wild-type (non-WT) echinocandin MIC values were sequenced for hot spot (HS) mutations. Rezafungin inhibited 99.8% of Candida albicans isolates (MIC(50/90), 0.03/0.06 μg/ml), 95.7% of Candida glabrata isolates (MIC(50/90), 0.06/0.12 μg/ml), 97.4% of Candida tropicalis isolates (MIC(50/90), 0.03/0.06 μg/ml), 100.0% of Candida krusei isolates (MIC(50/90), 0.03/0.06 μg/ml), and 100.0% of Candida dubliniensis isolates (MIC(50/90), 0.06/0.12 μg/ml) at ≤0.12 μg/ml. All (329/329 [100.0%]) Candida parapsilosis isolates (MIC(50/90),1/2 μg/ml) were inhibited by rezafungin at ≤4 μg/ml. Fluconazole resistance was detected among 8.6% of C. glabrata isolates, 12.5% of C. parapsilosis isolates, 3.2% of C. dubliniensis isolates, and 2.6% of C. tropicalis isolates. The activity of rezafungin against these 6 Candida spp. was similar to the activity of the other echinocandins. Detection of the HS mutation was performed by sequencing echinocandin-resistant or non-WT Candida isolates. Good activity against C. neoformans was observed for fluconazole and the other azoles, whereas the echinocandins, including rezafungin, displayed limited activity. Rezafungin displayed activity similar to that of the other echinocandins against A. fumigatus and A. flavus. These in vitro data contribute to accumulating research demonstrating the potential of rezafungin for preventing and treating invasive fungal infections.
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spelling pubmed-71792612020-04-24 Activity of a Long-Acting Echinocandin, Rezafungin, and Comparator Antifungal Agents Tested against Contemporary Invasive Fungal Isolates (SENTRY Program, 2016 to 2018) Pfaller, Michael A. Carvalhaes, Cecilia Messer, Shawn A. Rhomberg, Paul R. Castanheira, Mariana Antimicrob Agents Chemother Susceptibility We evaluated the activity of rezafungin and comparators, using Clinical and Laboratory Standards Institute (CLSI) broth microdilution methods, against a worldwide collection of 2,205 invasive fungal isolates recovered from 2016 to 2018. Candida (n = 1,904 isolates; 6 species), Cryptococcus neoformans (n = 73), Aspergillus fumigatus (n = 183), and Aspergillus flavus (n = 45) isolates were tested for their susceptibility (S) to rezafungin as well as the comparators caspofungin, anidulafungin, micafungin, and azoles. Interpretive criteria were applied following CLSI published clinical breakpoints (CBPs) and epidemiological cutoff values (ECVs). Isolates displaying non-wild-type (non-WT) echinocandin MIC values were sequenced for hot spot (HS) mutations. Rezafungin inhibited 99.8% of Candida albicans isolates (MIC(50/90), 0.03/0.06 μg/ml), 95.7% of Candida glabrata isolates (MIC(50/90), 0.06/0.12 μg/ml), 97.4% of Candida tropicalis isolates (MIC(50/90), 0.03/0.06 μg/ml), 100.0% of Candida krusei isolates (MIC(50/90), 0.03/0.06 μg/ml), and 100.0% of Candida dubliniensis isolates (MIC(50/90), 0.06/0.12 μg/ml) at ≤0.12 μg/ml. All (329/329 [100.0%]) Candida parapsilosis isolates (MIC(50/90),1/2 μg/ml) were inhibited by rezafungin at ≤4 μg/ml. Fluconazole resistance was detected among 8.6% of C. glabrata isolates, 12.5% of C. parapsilosis isolates, 3.2% of C. dubliniensis isolates, and 2.6% of C. tropicalis isolates. The activity of rezafungin against these 6 Candida spp. was similar to the activity of the other echinocandins. Detection of the HS mutation was performed by sequencing echinocandin-resistant or non-WT Candida isolates. Good activity against C. neoformans was observed for fluconazole and the other azoles, whereas the echinocandins, including rezafungin, displayed limited activity. Rezafungin displayed activity similar to that of the other echinocandins against A. fumigatus and A. flavus. These in vitro data contribute to accumulating research demonstrating the potential of rezafungin for preventing and treating invasive fungal infections. American Society for Microbiology 2020-03-24 /pmc/articles/PMC7179261/ /pubmed/32015043 http://dx.doi.org/10.1128/AAC.00099-20 Text en Copyright © 2020 Pfaller et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Susceptibility
Pfaller, Michael A.
Carvalhaes, Cecilia
Messer, Shawn A.
Rhomberg, Paul R.
Castanheira, Mariana
Activity of a Long-Acting Echinocandin, Rezafungin, and Comparator Antifungal Agents Tested against Contemporary Invasive Fungal Isolates (SENTRY Program, 2016 to 2018)
title Activity of a Long-Acting Echinocandin, Rezafungin, and Comparator Antifungal Agents Tested against Contemporary Invasive Fungal Isolates (SENTRY Program, 2016 to 2018)
title_full Activity of a Long-Acting Echinocandin, Rezafungin, and Comparator Antifungal Agents Tested against Contemporary Invasive Fungal Isolates (SENTRY Program, 2016 to 2018)
title_fullStr Activity of a Long-Acting Echinocandin, Rezafungin, and Comparator Antifungal Agents Tested against Contemporary Invasive Fungal Isolates (SENTRY Program, 2016 to 2018)
title_full_unstemmed Activity of a Long-Acting Echinocandin, Rezafungin, and Comparator Antifungal Agents Tested against Contemporary Invasive Fungal Isolates (SENTRY Program, 2016 to 2018)
title_short Activity of a Long-Acting Echinocandin, Rezafungin, and Comparator Antifungal Agents Tested against Contemporary Invasive Fungal Isolates (SENTRY Program, 2016 to 2018)
title_sort activity of a long-acting echinocandin, rezafungin, and comparator antifungal agents tested against contemporary invasive fungal isolates (sentry program, 2016 to 2018)
topic Susceptibility
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179261/
https://www.ncbi.nlm.nih.gov/pubmed/32015043
http://dx.doi.org/10.1128/AAC.00099-20
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