Detection of beta-lactamase production in clinical Prevotella species by MALDI-TOF MS method.


Journal

Anaerobe
ISSN: 1095-8274
Titre abrégé: Anaerobe
Pays: England
ID NLM: 9505216

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 14 05 2020
revised: 08 07 2020
accepted: 09 07 2020
pubmed: 10 8 2020
medline: 23 6 2021
entrez: 10 8 2020
Statut: ppublish

Résumé

Penicillins, can be used in treatment of infections due to Prevotella species if they are susceptible to penicillin. Early and accurate preliminary detection of β-lactamase-producing isolates is crucial for treatment of infection. The aim of this study was to determine β-lactamase-producing Prevotella species by MALDI-TOF MS and screen them for the presence of cfxA gene, responsible for β-lactamase production. A total of 500 clinically relevant Prevotella isolates, collected from 13 countries for the previous European antibiotic resistance surveillance study, were tested. Susceptibility testing was performed against ampicillin and ampicillin/sulbactam by Etest methodology. EUCAST guidelines were used for susceptibility interpretations; the isolates with MIC value ≤ 0.5 for ampicillin were considered susceptible and >2 resistant. All Prevotella isolates, were tested for detection of β-lactamase activity by MALDI-TOF MS (Vitek® MS Research Use Only) system and the presence of the cfxA gene by PCR method. The susceptibility levels of the isolates to ampicillin/sulbactam and ampicillin were 99.6% and 43.4%, respectively. A total 59% of isolates presented β-lactamase activity and 60.8% were cfxA gene positive. Both these tests were positive for isolates in the resistant category. Additionally, >95% of the isolates (n = 65) which ampicillin MIC values ranged from >0.5 μg/mL to 2 μg/ml displayed β-lactamase activity. We also found that the MALDI-TOF MS-based β-lactamase assay delivers results in 2 h. We found a high concordance between the MALDI-TOF MS β-lactamase results in terms of cfxA β-lactamase gene presence. MALDI-TOF MS may serve as a simple and efficient alternative method of the existing phenotypic and PCR-based methods.

Identifiants

pubmed: 32768494
pii: S1075-9964(20)30096-2
doi: 10.1016/j.anaerobe.2020.102240
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
beta-Lactamases EC 3.5.2.6

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

102240

Investigateurs

Eva Leitner (E)
Ingrid Wybo (I)
Vesna Tripkovic (V)
Ulrik S Justesen (US)
Helene Jean-Pierre (H)
Suzana C Stingu (SC)
Arne C Rodloff (AC)
Joseph Paparaskevas (J)
Edit Urban (E)
Wafaa Jamal (W)
Vincent O Rotimi (VO)
Alida C M Veloo (ACM)
Samo Jeverica (S)
Guven Kulekci (G)
Hrisi B Tokman (HB)
Trefor Morris (T)

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors; Professor E. Nagy, J.Soki and N. Ulger Toprak were members of ESGAI, Professor G. Soyletir and O. Akgul have no conflicts of interest to declare.

Auteurs

Nurver Ulger Toprak (NU)

Marmara University School of Medicine, Department of Microbiology, Istanbul, Turkey. Electronic address: nulger@marmara.edu.tr.

Oncu Akgul (O)

Marmara University School of Medicine, Department of Microbiology, Istanbul, Turkey.

József Sóki (J)

Institute of Clinical Microbiology, University of Szeged, Szeged, Hungary.

Guner Soyletir (G)

Marmara University School of Medicine, Department of Microbiology, Istanbul, Turkey.

Elisabeth Nagy (E)

Institute of Clinical Microbiology, University of Szeged, Szeged, Hungary.

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