Multicenter comparison of Etest, Vitek2 and BD Phoenix to broth microdilution for beta-lactam susceptibility testing of Streptococcus pneumonia.

Antimicrobial susceptibility testing Beta-lactam EUCAST breakpoints Streptococcus pneumoniae

Journal

European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology
ISSN: 1435-4373
Titre abrégé: Eur J Clin Microbiol Infect Dis
Pays: Germany
ID NLM: 8804297

Informations de publication

Date de publication:
27 May 2024
Historique:
received: 27 12 2023
accepted: 04 05 2024
medline: 27 5 2024
pubmed: 27 5 2024
entrez: 27 5 2024
Statut: aheadofprint

Résumé

To assess performance of Etest®, Vitek®2 and BD Phoenix™ to determine the susceptibility of Streptococcus pneumoniae strains to penicillin, ampicillin and cefotaxime. Sixty unique S. pneumoniae challenge strains were selected to cover a wide range of penicillin, ampicillin and cefotaxime minimal inhibitory concentrations (MICs). Strains were analyzed in four different Belgian laboratories. Etest® benzylpenicillin (BEN), ampicillin/amoxicillin (AMP) and cefotaxime (CTA) (bioMérieux), Vitek®2 AST-ST03 (bioMérieux) and BD Phoenix™ SMIC/ID-11 testing were each performed in two different labs. Results were compared to Sensititre® broth microdilution (BMD) (Thermo Fisher Scientific) results. MIC results were interpreted using EUCAST non-meningitis breakpoints (v 13.0). Essential agreement (EA) was ≥ 90% for all methods compared to BMD, except for Etest® BEN on Oxoid plate (58.3%), Etest® AMP (both on Oxoid (65.8%) and BD BBL plate (84.2%)). Categorical agreement (CA) for penicillin was only ≥ 90% for Vitek®2, for other methods CA ranged between 74 and 84%. CA for AMP was for all methods < 90% (range 75.8-88.3%) and CA for CTA was between 87 and 90% for all methods except for Etest on Oxoid plate (79.2%). Our study indicates that Vitek®2 and BD Phoenix™ are reliable for providing accurate pneumococcal susceptibility results for BEN, AMP and CTA. Using Etest BEN or AMP on Oxoid plate carries a risk of underestimating the MIC and should be interpreted with caution, especially when the obtained MIC is 1 or 2 doubling dilutions below the S or R clinical breakpoint.

Identifiants

pubmed: 38801483
doi: 10.1007/s10096-024-04847-2
pii: 10.1007/s10096-024-04847-2
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : FOD Volksgezondheid, Veiligheid van de Voedselketen en Leefmilieu
ID : FOD Volksgezondheid, Veiligheid van de Voedselketen en Leefmilieu

Informations de copyright

© 2024. The Author(s).

Références

European Centre for Disease Prevention and Control (2022) Antimicrobial resistance in the EU/EEA (EARS-Net) - Annual Epidemiological Report 2021. ECDC, Stockholm
EUCAST (2019) Warning against the use of gradient tests for benzylpenicillin MIC in Streptococcus pneumoniae. https://www.eucast.org/fileadmin/src/media/PDFs/EUCAST_files/Warnings/Warnings_docs/Warning_-_gradient_for_benzyl_and_pnc_21nov2019b.pdf . Accessed 14 September 2023
CLSI (2015) Verification of Commercial Microbial Identification and Antimicrobial Susceptibility Testing Systems. 1st ed. CLSI guideline M52. Wayne, PA: Clinical and Laboratory Standards Institute
International Standard Organisation ISO 20776-2:2021 (2021) Clinical laboratory testing and in vitro diagnostic test systems_Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices. Part 2_Evaluation of performance of antimicrobial susceptibility test devices against reference broth micro-dilution AFNOR. Genève
The European Committee on Antimicrobial Susceptibility Testing (2023) Breakpoint tables for interpretation of MICs and zone diameters. Version 13.0
Humphries RM, Ambler J, Mitchell SL, Castanheira M, Dingle T, Hindler JA, Koeth L, Sei K, CLSI Methods Development and Standardization Working Group of the Subcommittee on Antimicrobial Susceptibility Testing (2018) CLSI Methods Development and Standardization Working Group Best Practices for Evaluation of Antimicrobial susceptibility tests. J Clin Microbiol 56(4):e01934–e01917. https://doi.org/10.1128/JCM.01934-17
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Auteurs

Steven Martens (S)

National Reference Center for Invasive Pneumococci, University Hospitals Leuven, Herestraat, 49, Leuven, 3000, Belgium.

Lize Cuypers (L)

National Reference Center for Invasive Pneumococci, University Hospitals Leuven, Herestraat, 49, Leuven, 3000, Belgium.
Laboratory of Clinical Microbiology, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.

Florian Bélik (F)

Laboratory of Clinical Microbiology, CHU UCL Namur and Université Catholique de Louvain, Yvoir, Belgium.

Pieter-Jan Briers (PJ)

Laboratory of Clinical Microbiology, Jessa Ziekenhuis, Hasselt, Belgium.

Pieter-Jan Ceyssens (PJ)

Unit of Human Bacterial Diseases, Sciensano, Brussels, Belgium.

Olivier Denis (O)

Laboratory of Clinical Microbiology, CHU UCL Namur and Université Catholique de Louvain, Yvoir, Belgium.

Te-Din Huang (TD)

Laboratory of Clinical Microbiology, CHU UCL Namur and Université Catholique de Louvain, Yvoir, Belgium.

Koen Magerman (K)

Laboratory of Clinical Microbiology, Jessa Ziekenhuis, Hasselt, Belgium.

Thomas Strypens (T)

Laboratory of Clinical Microbiology, AZ Sint-Lucas Ziekenhuis and Universiteit Gent, Gent, Belgium.

Anne-Marie Van den Abeele (AM)

Laboratory of Clinical Microbiology, AZ Sint-Lucas Ziekenhuis and Universiteit Gent, Gent, Belgium.

Stefanie Desmet (S)

National Reference Center for Invasive Pneumococci, University Hospitals Leuven, Herestraat, 49, Leuven, 3000, Belgium. stefanie.desmet@uzleuven.be.
Laboratory of Clinical Microbiology, Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium. stefanie.desmet@uzleuven.be.

Classifications MeSH