Multiple colony antifungal susceptibility testing detects polyresistance in clinical Candida cultures: a European Confederation of Medical Mycology excellence centers study.


Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
Sep 2022
Historique:
received: 07 02 2022
revised: 13 04 2022
accepted: 16 04 2022
pubmed: 11 5 2022
medline: 20 9 2022
entrez: 10 5 2022
Statut: ppublish

Résumé

Many factors influence the outcome of in vitro antifungal susceptibility testing (AFST), including endpoint definition, inoculum sizes, time and temperature of incubation, and growth medium used. This European Confederation of Medical Mycology (ECMM) Excellence center driven study investigated multiple colony testing (MCT) of five separate colonies to investigate the prevalence of polyresistance (PR), defined as heterogeneous MICs from a same-species Candida culture irrespective of the underlying resistance mechanism. Candida spp. MCT for fluconazole and anidulafungin was performed by Etest prospectively comprising 405 clinical samples. MCT results were compared to the real-life routine MIC data and PR was assessed. Candida colonies displaying strong PR were selected for genotyping using multilocus sequence typing and random amplified polymorphic DNA assays for C. lusitaniae. Candida PR was observed in 33 of 405 samples (8.1%), with higher rates for non-albicans species (26/186, 14%) than for C. albicans (7/219, 3.2%), and for fluconazole than for anidulafungin. MCT detected acquired resistance more often than routine AFST (18/405, 4.5%) and 9 of the 161 investigated blood cultures showed PR (5.6%). Multilocus sequence typing and random amplified polymorphic DNA did not reveal a uniform genetic correlate in strains studied. This study shows that Candida single MIC-values obtained in routine diagnostics may be incidental, as they fail to detect PR and resistant subpopulations reliably. The reasons for PR seem to be manifold and should be regarded as a phenotypical expression of genomic variability irrespective of the underlying resistance mechanism, which may help to interpret ambiguous and non-reproducible AFST results.

Identifiants

pubmed: 35537592
pii: S1198-743X(22)00222-1
doi: 10.1016/j.cmi.2022.04.014
pii:
doi:

Substances chimiques

Antifungal Agents 0
Fluconazole 8VZV102JFY
Anidulafungin 9HLM53094I

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1288.e1-1288.e7

Informations de copyright

Copyright © 2022. Published by Elsevier Ltd.

Auteurs

Miriam A Knoll (MA)

Institute of Hygiene and Medical Microbiology, ECMM Excellence Center, Medical University of Innsbruck, Innsbruck, Austria.

Nina Lackner (N)

Institute of Hygiene and Medical Microbiology, ECMM Excellence Center, Medical University of Innsbruck, Innsbruck, Austria.

Hanno Ulmer (H)

Department of Medical Statistics, Informatics and Health Economics, Medical University of Innsbruck, Innsbruck, Austria.

Eldina Samardzic (E)

Institute of Hygiene and Medical Microbiology, ECMM Excellence Center, Medical University of Innsbruck, Innsbruck, Austria.

Joerg Steinmann (J)

Institute of Clinical Hygiene, Medical Microbiology and Infectiology, Paracelsus Medical University, Klinikum, Nurnberg, Germany; Institute of Medical Microbiology, ECMM Excellence Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

Robert Krause (R)

Biotechmed, Graz, Austria; Division of Infectious Diseases, ECMM Excellence Center, Department of Internal Medicine, Medical University of Graz, Austria.

Hedda L Verhasselt (HL)

Institute of Medical Microbiology, ECMM Excellence Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

Peter-Michael Rath (PM)

Institute of Medical Microbiology, ECMM Excellence Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.

Frieder Fuchs (F)

Institute for Medical Microbiology, Immunology and Hygiene, University of Cologne, Medical Faculty and University Hospital of Cologne, Cologne, Germany; Department of Microbiology and Hospital Hygiene, Bundeswehr Central Hospital Koblenz, Koblenz, Germany.

Philipp Koehler (P)

Department I of Internal Medicine, ECMM Excellence Center, Critical Care Medicine, University Hospital of Cologne, Cologne, Germany; Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany.

Blandine Denis (B)

Infectious Diseases Department, ECMM Excellence Center, Hôpital Saint-Louis, APHP, Paris, France.

Samia Hamane (S)

Infectious Diseases Department, ECMM Excellence Center, Hôpital Saint-Louis, APHP, Paris, France; Mycology-Parasitology Department, Hôpital Saint-Louis, APHP, Paris, France.

Alexandre Alanio (A)

Mycology-Parasitology Department, Hôpital Saint-Louis, APHP, Paris, France; Université de Paris, Molecular Mycology Unit, CNRS UMR2000, National Reference Centre for Invasive Mycoses and Antifungals, Institut Pasteur, Université de Paris, Paris, France.

Cornelia Lass-Flörl (C)

Institute of Hygiene and Medical Microbiology, ECMM Excellence Center, Medical University of Innsbruck, Innsbruck, Austria. Electronic address: cornelia.lass-floerl@i-med.ac.at.

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Classifications MeSH