A European multicenter evaluation study to investigate the performance on commercially available selective agar plates for the detection of carbapenemase producing Enterobacteriaceae
0301 basic medicine
antibiotic resistance
Selective agar
carbapenemases
Carbapenem resistance
Swine
carbapenem resistance
résistance aux antibiotiques
entérobactérie
Microbial Sensitivity Tests
MESH: Carbapenem-Resistant Enterobacteriaceae
Sensitivity and Specificity
Article
beta-Lactamases
03 medical and health sciences
Enterobacteriaceae
Bacterial Proteins
Salmonella
[SDV.IDA]Life Sciences [q-bio]/Food engineering
Animals
animal
résistance
microbiologie
selective agar
MESH: Enterobacteriaceae Infections
MESH: Swine
agar
bactérie
2. Zero hunger
MESH: Microbial Sensitivity Tests
Bacteriological Techniques
Animal
microbiology
article
ddc:630
Enterobacteriaceae Infections
IMPART
Carbapenemases
[SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/Bacteriology
MESH: Sensitivity and Specificity
Text
Agar
veterinary medicine
Carbapenem-Resistant Enterobacteriaceae
carbapénème
DOI:
10.1016/j.mimet.2022.106418
Publication Date:
2022-01-15T15:49:47Z
AUTHORS (17)
ABSTRACT
The European Food Safety Authority (EFSA) advised to prioritize monitoring carbapenemase producing Enterobacteriaceae (CPE) in food producing animals. Therefore, this study evaluated the performance of different commercially available selective agars for the detection of CPE using spiked pig caecal and turkey meat samples and the proposed EFSA cultivation protocol. Eleven laboratories from nine countries received eight samples (four caecal and four meat samples). For each matrix, three samples contained approximately 100 CFU/g CPE, and one sample lacked CPE. After overnight enrichment in buffered peptone water, broths were spread upon Brilliance™ CRE Agar (1), CHROMID® CARBA (2), CHROMagar™ mSuperCARBA™ (3), Chromatic™ CRE (4), CHROMID® OXA-48 (5) and Chromatic™ OXA-48 (6). From plates with suspected growth, one to three colonies were selected for species identification, confirmation of carbapenem resistance and detection of carbapenemase encoding genes, by methods available at participating laboratories. Of the eleven participating laboratories, seven reported species identification, susceptibility tests and genotyping on isolates from all selective agar plates. Agars 2, 4 and 5 performed best, with 100% sensitivity. For agar 3, a sensitivity of 96% was recorded, while agar 1 and 6 performed with 75% and 43% sensitivity, respectively. More background flora was noticed for turkey meat samples than pig caecal samples. Based on this limited set of samples, most commercially available agars performed adequately. The results indicate, however, that OXA-48-like and non-OXA-48-like producers perform very differently, and one should consider which CPE strains are of interest to culture when choosing agar type.
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