Burkholderia pseudomallei multi-centre study to establish EUCAST MIC and zone diameter distributions and epidemiological cut-off values.

Antimicrobial susceptibility testing Broth microdilution Clinical breakpoints Disc diffusion ECOFF MIC determination Melioidosis Minimum inhibitory concentration Quality control

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:
09 Jul 2020
Historique:
received: 05 05 2020
revised: 26 06 2020
accepted: 01 07 2020
pubmed: 13 7 2020
medline: 13 7 2020
entrez: 13 7 2020
Statut: aheadofprint

Résumé

Melioidosis, caused by Burkholderia pseudomallei, requires intensive antimicrobial treatment. However, standardized antimicrobial susceptibility testing (AST) methodology based on modern principles for determining breakpoints and ascertaining performance of methods are lacking for B. pseudomallei. This study aimed to establish MIC and zone diameter distributions on which to set epidemiological cut-off (ECOFF) values for B. pseudomallei using standard EUCAST methodology for non-fastidious organisms. Non-consecutive, non-duplicate clinical B. pseudomallei isolates (9-70 per centre) were tested at eight study centres against eight antimicrobials by broth microdilution (BMD) and the EUCAST disc diffusion method. Isolates without and with suspected resistance mechanisms were deliberately selected. The EUCAST Development Laboratory ensured the quality of study materials, and provided guidance on performance of the tests and interpretation of results. Aggregated results were analysed according to EUCAST recommendations to determine ECOFFs. MIC and zone diameter distributions were generated using BMD and disc diffusion results obtained for 361 B. pseudomallei isolates. MIC and zone diameter ECOFFs (mg/L; mm) were determined for amoxicillin-clavulanic acid (8; 22), ceftazidime (8; 22), imipenem (2; 29), meropenem (2; 26), doxycycline (2; none), tetracycline (8; 23), chloramphenicol (8; 22) and trimethoprim-sulfamethoxazole (4; 28). We have validated the use of standard BMD and disc diffusion methodology for AST of B. pseudomallei. The MIC and zone diameter distributions generated in this study allowed us to establish MIC and zone diameter ECOFFs for the antimicrobials studied. These ECOFFs served as background data for EUCAST to set clinical MIC and zone diameter breakpoints for B. pseudomallei.

Identifiants

pubmed: 32653660
pii: S1198-743X(20)30384-0
doi: 10.1016/j.cmi.2020.07.001
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

O Karatuna (O)

EUCAST Development Laboratory, Växjö, Sweden. Electronic address: onur.karatuna@kronoberg.se.

D A B Dance (DAB)

Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Vientiane, Lao People's Democratic Republic; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK; Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.

E Matuschek (E)

EUCAST Development Laboratory, Växjö, Sweden.

J Åhman (J)

EUCAST Development Laboratory, Växjö, Sweden.

P Turner (P)

Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK; Cambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.

J Hopkins (J)

Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK; Cambodia Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia.

P Amornchai (P)

Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.

V Wuthiekanun (V)

Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.

T-P Cusack (TP)

Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Vientiane, Lao People's Democratic Republic; National Infection Service, Public Health England, London, UK.

R Baird (R)

Royal Darwin Hospital, Darwin, NT, Australia.

J Hennessy (J)

Royal Darwin Hospital, Darwin, NT, Australia.

R Norton (R)

Townsville Hospital, Townsville, QLD, Australia.

M Armstrong (M)

Townsville Hospital, Townsville, QLD, Australia.

S Zange (S)

Bundeswehr Institute of Microbiology, Munich, Germany.

L Zoeller (L)

Bundeswehr Institute of Microbiology, Munich, Germany.

T Wahab (T)

Public Health Agency of Sweden, Stockholm, Sweden.

D Jacob (D)

Robert Koch Institute, Berlin, Germany.

R Grunow (R)

Robert Koch Institute, Berlin, Germany.

G Kahlmeter (G)

EUCAST Development Laboratory, Växjö, Sweden.

Classifications MeSH