MIC distributions for amphotericin B, fluconazole, itraconazole, voriconazole, flucytosine and anidulafungin and 35 uncommon pathogenic yeast species from the UK determined using the CLSI broth microdilution method.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
01 05 2020
Historique:
received: 19 06 2019
revised: 17 10 2019
accepted: 19 12 2019
pubmed: 7 2 2020
medline: 25 6 2021
entrez: 7 2 2020
Statut: ppublish

Résumé

Epidemiological cut-off values and clinical interpretive breakpoints have been developed for a number of antifungal agents with the most common Candida species that account for the majority of infections due to pathogenic yeasts species. However, less-common species, for which susceptibility data are limited, are increasingly reported in high-risk patients and breakthrough infections. The UK National Mycology Reference Laboratory performs routine antifungal susceptibility testing of clinical yeast isolates submitted from across the UK. Between 2002 and 2016, >32 000 isolates representing 94 different yeast species were referred to the laboratory. Here we present antifungal susceptibility profiles generated over this period for amphotericin B, fluconazole, voriconazole, itraconazole, anidulafungin and flucytosine against 35 species of uncommon yeast using CLSI methodologies. MIC data were interpreted against epidemiological cut-off values and clinical breakpoints developed with Candida albicans, in order to identify species with unusually skewed MIC distributions that potentially indicate resistance. Potential resistance to at least one antifungal agent (>10% of isolates with MICs greater than the epidemiological cut-off or clinical breakpoint) was evidenced for 29/35 species examined here. Four species exhibited elevated MICs with all of the triazole antifungal drugs against which they were tested, and 21 species exhibited antifungal resistance to agents from at least two different classes of antifungal agent. This study highlights a number of yeast species with unusual MIC distributions and provides data to aid clinicians in deciding which antifungal regimens may be appropriate when confronted with infections with rarer yeasts.

Sections du résumé

BACKGROUND
Epidemiological cut-off values and clinical interpretive breakpoints have been developed for a number of antifungal agents with the most common Candida species that account for the majority of infections due to pathogenic yeasts species. However, less-common species, for which susceptibility data are limited, are increasingly reported in high-risk patients and breakthrough infections.
METHODS
The UK National Mycology Reference Laboratory performs routine antifungal susceptibility testing of clinical yeast isolates submitted from across the UK. Between 2002 and 2016, >32 000 isolates representing 94 different yeast species were referred to the laboratory. Here we present antifungal susceptibility profiles generated over this period for amphotericin B, fluconazole, voriconazole, itraconazole, anidulafungin and flucytosine against 35 species of uncommon yeast using CLSI methodologies. MIC data were interpreted against epidemiological cut-off values and clinical breakpoints developed with Candida albicans, in order to identify species with unusually skewed MIC distributions that potentially indicate resistance.
RESULTS
Potential resistance to at least one antifungal agent (>10% of isolates with MICs greater than the epidemiological cut-off or clinical breakpoint) was evidenced for 29/35 species examined here. Four species exhibited elevated MICs with all of the triazole antifungal drugs against which they were tested, and 21 species exhibited antifungal resistance to agents from at least two different classes of antifungal agent.
CONCLUSIONS
This study highlights a number of yeast species with unusual MIC distributions and provides data to aid clinicians in deciding which antifungal regimens may be appropriate when confronted with infections with rarer yeasts.

Identifiants

pubmed: 32025716
pii: 5727899
doi: 10.1093/jac/dkz568
doi:

Substances chimiques

Antifungal Agents 0
Itraconazole 304NUG5GF4
Amphotericin B 7XU7A7DROE
Fluconazole 8VZV102JFY
Anidulafungin 9HLM53094I
Flucytosine D83282DT06
Voriconazole JFU09I87TR

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1194-1205

Informations de copyright

© Crown copyright 2020.

Auteurs

Andrew M Borman (AM)

PHE UK National Mycology Reference Laboratory, Science Quarter, Southmead Hospital, Bristol, UK.

Julian Muller (J)

PHE UK National Mycology Reference Laboratory, Science Quarter, Southmead Hospital, Bristol, UK.

Jo Walsh-Quantick (J)

PHE UK National Mycology Reference Laboratory, Science Quarter, Southmead Hospital, Bristol, UK.

Adrien Szekely (A)

PHE UK National Mycology Reference Laboratory, Science Quarter, Southmead Hospital, Bristol, UK.

Zoe Patterson (Z)

PHE UK National Mycology Reference Laboratory, Science Quarter, Southmead Hospital, Bristol, UK.

Michael D Palmer (MD)

PHE UK National Mycology Reference Laboratory, Science Quarter, Southmead Hospital, Bristol, UK.

Mark Fraser (M)

PHE UK National Mycology Reference Laboratory, Science Quarter, Southmead Hospital, Bristol, UK.

Elizabeth M Johnson (EM)

PHE UK National Mycology Reference Laboratory, Science Quarter, Southmead Hospital, Bristol, UK.

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Classifications MeSH