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Journal of Microbiological Methods

dc.contributor.authorDierikx, Cindy
dc.contributor.authorBörjesson, Stefan
dc.contributor.authorPerrin-Guyomard, Agnes
dc.contributor.authorHaenni, Marisa
dc.contributor.authorNorstrom, Madelaine
dc.contributor.authorDivon, Hege H.
dc.contributor.authorKarin Ilag, Hanna
dc.contributor.authorGranier, Sophie A.
dc.contributor.authorHammerum, Annette
dc.contributor.authorSejer Kjeldgaard, Jette
dc.contributor.authorPauly, Natalie
dc.contributor.authorRandall, Luke
dc.contributor.authorAnjum, Muna F.
dc.contributor.authorŚmiałowska, Aleksandra
dc.contributor.authorFranco, Alessia
dc.contributor.authorVeldman, Kees
dc.contributor.authorSchau Slettemeas, Jannice
dc.date.accessioned2022-01-31T09:55:47Z
dc.date.available2022-01-31T09:55:47Z
dc.date.issued2022
dc.identifierhttps://dspace.piwet.pulawy.pl/xmlui/handle/123456789/186
dc.identifier.issn0167-7012
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0167701222000136?via%3Dihub
dc.description.abstractThe 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.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectSelective agaren_US
dc.subjectCarbapenem resistanceen_US
dc.subjectCarbapenemasesen_US
dc.subjectEnterobacteriaceaeen_US
dc.subjectSalmonellaen_US
dc.titleA European multicenter evaluation study to investigate the performance on commercially available selective agar plates for the detection of carbapenemase producing Enterobacteriaceaeen_US
dc.typeArticleen_US
dcterms.bibliographicCitation2022 v.193 (106418)
dcterms.titleJournal of Microbiological Methods
dc.identifier.doihttps://doi.org/10.1016/j.mimet.2022.106418


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