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dc.contributor.authorPark, Mi Jung-
dc.contributor.authorPark, Yeon-Joon-
dc.contributor.authorOh, Eun-Jee-
dc.contributor.authorChang, Jiyoung-
dc.contributor.authorKim, Youngsic-
dc.contributor.authorYu, Jinkyung-
dc.contributor.authorPark, Kang Gyun-
dc.contributor.authorAhn, Dae-Ro-
dc.date.accessioned2024-01-20T03:00:19Z-
dc.date.available2024-01-20T03:00:19Z-
dc.date.created2021-09-05-
dc.date.issued2016-12-
dc.identifier.issn0167-7012-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/123380-
dc.description.abstractResistance to third generation cephalosporins is widely disseminated in Enterobacteriaceae mainly due to extended-spectrum-beta-lactamases, plasmid AmpC beta-lactamases, and hyperproduction of chromosomal AmpC beta-lactamases. Here we evaluated the performance of a novel fluorogenic probe rapid test and compared the results with the phenol red assay using a total of 77 characterized organisms (44 extended-spectrum-beta-lactamases, 33 chromosomal or plasmid AmpC(3-lactamases) and 46 susceptible organisms. The fluorescent assay showed higher sensitivity than the phenol red assay in cefotaximase type extended-spectrum-beta-lactamases, non-cefotaximase type extended-spectrum-beta-lactamases, chromosomal AmpC beta-lactamases, and plasmid AmpC plactamases (96.7% vs. 90.0%, p = 0.157; 71.4% vs. 7.1%, p = 0.003; 100.0% vs. 64.7%, p < 0.001; 100.0% vs. 6.3%, p < 0.001). The fluorescent assay had a positive correlation with the exponents of cefotaxime and ceftazidime minimum inhibitory concentrations (p < 0.001 for both). The new fluorescent assay will be very useful for the rapid detection of resistance to third generation cephalosporins that originates from various beta-lactamases. (C) 2016 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectLACTAMASE-PRODUCING ENTEROBACTERIACEAE-
dc.subjectBETA-LACTAMASES-
dc.subjectRAPID DETECTION-
dc.subjectIMPACT-
dc.titlePerformance of a novel fluorogenic chimeric analog for the detection of third-generation cephalosporin resistant bacteria-
dc.typeArticle-
dc.identifier.doi10.1016/j.mimet.2016.10.016-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF MICROBIOLOGICAL METHODS, v.131, pp.161 - 165-
dc.citation.titleJOURNAL OF MICROBIOLOGICAL METHODS-
dc.citation.volume131-
dc.citation.startPage161-
dc.citation.endPage165-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000390517000025-
dc.identifier.scopusid2-s2.0-84994056656-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaMicrobiology-
dc.type.docTypeArticle-
dc.subject.keywordPlusLACTAMASE-PRODUCING ENTEROBACTERIACEAE-
dc.subject.keywordPlusBETA-LACTAMASES-
dc.subject.keywordPlusRAPID DETECTION-
dc.subject.keywordPlusIMPACT-
dc.subject.keywordAuthorExtended-spectrum-beta-lactamase-
dc.subject.keywordAuthorAmpC beta-lactamase-
dc.subject.keywordAuthorFluorogenic probe-
dc.subject.keywordAuthorPhenol red assay-
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