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Emergence of resistant Candida glabrata in Germany

BACKGROUND: Candida glabrata is the second leading fungal pathogen causing candidaemia and invasive candidiasis in Europe. This yeast is recognized for its rapid ability to acquire antifungal drug resistance. OBJECTIVES: We systematically evaluated 176 C. glabrata isolates submitted to the German Na...

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Autores principales: Aldejohann, Alexander Maximilian, Herz, Michaela, Martin, Ronny, Walther, Grit, Kurzai, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346698/
https://www.ncbi.nlm.nih.gov/pubmed/34377983
http://dx.doi.org/10.1093/jacamr/dlab122
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author Aldejohann, Alexander Maximilian
Herz, Michaela
Martin, Ronny
Walther, Grit
Kurzai, Oliver
author_facet Aldejohann, Alexander Maximilian
Herz, Michaela
Martin, Ronny
Walther, Grit
Kurzai, Oliver
author_sort Aldejohann, Alexander Maximilian
collection PubMed
description BACKGROUND: Candida glabrata is the second leading fungal pathogen causing candidaemia and invasive candidiasis in Europe. This yeast is recognized for its rapid ability to acquire antifungal drug resistance. OBJECTIVES: We systematically evaluated 176 C. glabrata isolates submitted to the German National Reference Center for Invasive Fungal Infections (NRZMyk) between 2015 and 2019 with regard to echinocandin and fluconazole susceptibility. METHODS: Susceptibility testing was performed using a reference protocol (EUCAST) and a range of commercial assays. Hot spot regions of the echinocandin target FKS genes were sequenced using Sanger sequencing. RESULTS: In total, 84 of 176 isolates were initially classified as anidulafungin-resistant based on EUCAST testing. Of those, 71 harboured mutations in the glucan synthase encoding FKS genes (13% in FKS1, 87% in FKS2). Significant differences in anidulafungin MICs were found between distinct mutation sites. 11 FKS wild-type (WT) isolates initially classified as resistant exhibited anidulafungin MICs fluctuating around the interpretation breakpoint upon re-testing with multiple assays. Two FKS WT isolates consistently showed high anidulafungin MICs and thus must be considered resistant despite the absence of target gene mutations. Over one-third of echinocandin-resistant strains displayed concomitant fluconazole resistance. Of those, isolates linked to bloodstream infection carrying a change at Ser-663 were associated with adverse clinical outcome. CONCLUSIONS: Resistant C. glabrata strains are emerging in Germany. Phenotypic echinocandin testing can result in misclassification of susceptible strains. FKS genotyping aids in detecting these strains, however, echinocandin resistance may occur despite a wild-type FKS genotype.
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spelling pubmed-83466982021-08-09 Emergence of resistant Candida glabrata in Germany Aldejohann, Alexander Maximilian Herz, Michaela Martin, Ronny Walther, Grit Kurzai, Oliver JAC Antimicrob Resist Original Article BACKGROUND: Candida glabrata is the second leading fungal pathogen causing candidaemia and invasive candidiasis in Europe. This yeast is recognized for its rapid ability to acquire antifungal drug resistance. OBJECTIVES: We systematically evaluated 176 C. glabrata isolates submitted to the German National Reference Center for Invasive Fungal Infections (NRZMyk) between 2015 and 2019 with regard to echinocandin and fluconazole susceptibility. METHODS: Susceptibility testing was performed using a reference protocol (EUCAST) and a range of commercial assays. Hot spot regions of the echinocandin target FKS genes were sequenced using Sanger sequencing. RESULTS: In total, 84 of 176 isolates were initially classified as anidulafungin-resistant based on EUCAST testing. Of those, 71 harboured mutations in the glucan synthase encoding FKS genes (13% in FKS1, 87% in FKS2). Significant differences in anidulafungin MICs were found between distinct mutation sites. 11 FKS wild-type (WT) isolates initially classified as resistant exhibited anidulafungin MICs fluctuating around the interpretation breakpoint upon re-testing with multiple assays. Two FKS WT isolates consistently showed high anidulafungin MICs and thus must be considered resistant despite the absence of target gene mutations. Over one-third of echinocandin-resistant strains displayed concomitant fluconazole resistance. Of those, isolates linked to bloodstream infection carrying a change at Ser-663 were associated with adverse clinical outcome. CONCLUSIONS: Resistant C. glabrata strains are emerging in Germany. Phenotypic echinocandin testing can result in misclassification of susceptible strains. FKS genotyping aids in detecting these strains, however, echinocandin resistance may occur despite a wild-type FKS genotype. Oxford University Press 2021-08-07 /pmc/articles/PMC8346698/ /pubmed/34377983 http://dx.doi.org/10.1093/jacamr/dlab122 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Aldejohann, Alexander Maximilian
Herz, Michaela
Martin, Ronny
Walther, Grit
Kurzai, Oliver
Emergence of resistant Candida glabrata in Germany
title Emergence of resistant Candida glabrata in Germany
title_full Emergence of resistant Candida glabrata in Germany
title_fullStr Emergence of resistant Candida glabrata in Germany
title_full_unstemmed Emergence of resistant Candida glabrata in Germany
title_short Emergence of resistant Candida glabrata in Germany
title_sort emergence of resistant candida glabrata in germany
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8346698/
https://www.ncbi.nlm.nih.gov/pubmed/34377983
http://dx.doi.org/10.1093/jacamr/dlab122
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