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Quality of MALDI-TOF mass spectra in routine diagnostics: results from an international external quality assessment including 36 laboratories from 12 countries using 47 challenging bacterial strains

A. Cuénod, M. Aerni, C. Bagutti, B. Bayraktar, ES. Boz, CB. Carneiro, C. Casanova, AT. Coste, P. Damborg, DW. van Dam, M. Demirci, P. Drevinek, O. Dubuis, J. Fernandez, G. Greub, J. Hrabak, G. Hürkal Yiğitler, J. Hurych, TG. Jensen, G. Jost, GA....

. 2023 ; 29 (2) : 190-199. [pub] 20220525

Jazyk angličtina Země Anglie, Velká Británie

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc23004463

OBJECTIVES: Matrix assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry (MS) is a widely used method for bacterial species identification. Incomplete databases and mass spectral quality (MSQ) still represent major challenges. Important proxies for MSQ are the number of detected marker masses, reproducibility, and measurement precision. We aimed to assess MSQs across diagnostic laboratories and the potential of simple workflow adaptations to improve it. METHODS: For baseline MSQ assessment, 47 diverse bacterial strains, which are challenging to identify by MALDI-TOF MS, were routinely measured in 36 laboratories from 12 countries, and well-defined MSQ features were used. After an intervention consisting of detailed reported feedback and instructions on how to acquire MALDI-TOF mass spectra, measurements were repeated and MSQs were compared. RESULTS: At baseline, we observed heterogeneous MSQ between the devices, considering the median number of marker masses detected (range = [2-25]), reproducibility between technical replicates (range = [55%-86%]), and measurement error (range = [147 parts per million (ppm)-588 ppm]). As a general trend, the spectral quality was improved after the intervention for devices, which yielded low MSQs in the baseline assessment as follows: for four out of five devices with a high measurement error, the measurement precision was improved (p-values <0.001, paired Wilcoxon test); for six out of ten devices, which detected a low number of marker masses, the number of detected marker masses increased (p-values <0.001, paired Wilcoxon test). DISCUSSION: We have identified simple workflow adaptations, which, to some extent, improve MSQ of poorly performing devices and should be considered by laboratories yielding a low MSQ. Improving MALDI-TOF MSQ in routine diagnostics is essential for increasing the resolution of bacterial identification by MALDI-TOF MS, which is dependent on the reproducible detection of marker masses. The heterogeneity identified in this external quality assessment (EQA) requires further study.

ADMED Microbiologie La Chaux de Fonds Switzerland

Applied Microbiology Research Department of Biomedicine University of Basel Basel Switzerland

Austrian Agency for Health and Food Safety Vienna Austria

Bioanalytica AG Lucerne Switzerland

Biomedical Center Faculty of Medicine in Pilsen Charles University Plzen Czech Republic

Cantonal Hospital Aarau Aarau Switzerland

Center for Laboratory Medicine St Gallen Switzerland

Clinical Laboratory AZNikolaas Sint Niklaas Belgium

Department of Clinical and Molecular Microbiology University Hospital Centre Zagreb Zagreb Croatia

Department of Clinical Microbiology Hvidovre Hospital Hvidovre Denmark

Department of Clinical Microbiology Odense University Hospital Odense Denmark

Department of Medical Microbiology 2nd Faculty of Medicine Charles University and Motol University Hospital Prague Czech Republic

Department of Medical Microbiology and Infection Prevention University of Groningen University Medical Center Groningen Groningen the Netherlands

Department of Medical Microbiology Kirklareli University Kirklareli Turkey

Department of Medical Microbiology University of Antwerp Belgium

Department of Medical Microbiology University of Health Sciences Haydarpasa Numune Teaching and Research Hospital Istanbul Turkey

Department of Veterinary and Animal Sciences University of Copenhagen Frederiksberg Denmark

Dianalabs Geneva Switzerland

Division of Clinical Bacteriology and Mycology University Hospital Basel Basel Switzerland

Division of Laboratory Medicine Laboratory of Bacteriology University Hospital of Geneva Geneva Switzerland

Eurofins Scientific AG Schönenwerd Switzerland

Hospital General Universitario Gregorio Maranon Madrid Spain

Institute for Infectious Diseases University of Bern Bern Switzerland

Institute of Medical Microbiology and Hygiene University of Tübingen Tübingen Germany

Institute of Microbiology University Hospital Lausanne Lausanne Switzerland

Institute of Veterinary Bacteriology University of Bern Bern Switzerland

Labor Team W Goldach Switzerland

Mabritec AG Riehen Switzerland

MCL Laboratories Niederwangen Switzerland

Reference Services Division UK Health Security Agency London United Kingdom

School of Public Health Ben Gurion University of the Negev and Soroka University Medical Center Beer Sheva Israel

State Laboratory Basel Stadt Basel Switzerland

UMC Utrecht Utrecht the Netherlands

University Hospital Freiburg Freiburg im Breisgau Germany

University Hospital of Wales Cardiff United Kingdom

University of Health Sciences Sisli Hamidiye Etfal Teaching and Research Hospital Istanbul Turkey

Viollier AG Allschwil Switzerland

Zuyderland MC Sittard the Netherlands

Citace poskytuje Crossref.org

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$a OBJECTIVES: Matrix assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry (MS) is a widely used method for bacterial species identification. Incomplete databases and mass spectral quality (MSQ) still represent major challenges. Important proxies for MSQ are the number of detected marker masses, reproducibility, and measurement precision. We aimed to assess MSQs across diagnostic laboratories and the potential of simple workflow adaptations to improve it. METHODS: For baseline MSQ assessment, 47 diverse bacterial strains, which are challenging to identify by MALDI-TOF MS, were routinely measured in 36 laboratories from 12 countries, and well-defined MSQ features were used. After an intervention consisting of detailed reported feedback and instructions on how to acquire MALDI-TOF mass spectra, measurements were repeated and MSQs were compared. RESULTS: At baseline, we observed heterogeneous MSQ between the devices, considering the median number of marker masses detected (range = [2-25]), reproducibility between technical replicates (range = [55%-86%]), and measurement error (range = [147 parts per million (ppm)-588 ppm]). As a general trend, the spectral quality was improved after the intervention for devices, which yielded low MSQs in the baseline assessment as follows: for four out of five devices with a high measurement error, the measurement precision was improved (p-values <0.001, paired Wilcoxon test); for six out of ten devices, which detected a low number of marker masses, the number of detected marker masses increased (p-values <0.001, paired Wilcoxon test). DISCUSSION: We have identified simple workflow adaptations, which, to some extent, improve MSQ of poorly performing devices and should be considered by laboratories yielding a low MSQ. Improving MALDI-TOF MSQ in routine diagnostics is essential for increasing the resolution of bacterial identification by MALDI-TOF MS, which is dependent on the reproducible detection of marker masses. The heterogeneity identified in this external quality assessment (EQA) requires further study.
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