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1.
J Microbiol Methods ; 221: 106938, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38642781

ABSTRACT

Current methods for plasmid-mediated AmpC ß-lactamase (pAmpC) detection in routine microbiological laboratories are based on various phenotypic tests. Eazyplex®SuperBug AmpC assay is a molecular assay based on isothermal amplification for rapid detection of the most common pAmpC types from bacterial culture: CMY-2 group, DHA, ACC and MOX. Our aim was to evaluate the diagnostic performance of this assay. The assay was evaluated on 64 clinical isolates of Enterobacterales without chromosomal inducible AmpC, and with phenotypically confirmed AmpC production. The results were confirmed, and isolates further characterized by whole-genome sequencing (WGS). eazyplex®SuperBug AmpC assay correctly detected the two most common pAmpC types CMY-2 group (16/16) and DHA (19/19). Detection of ACC and MOX could not be evaluated on our set of isolates since there was only one isolate harbouring ACC and none with MOX. pAmpC encoding genes could be detected in only eight of 36 investigated Escherichia coli isolates. The remaining 28 E. coli isolates harboured previously described mutations in the blaEC promoter, leading to the overexpression of chromosomally encoded E. coli specific AmpC ß-lactamase. All results were 100% concordant with the results of WGS. eazyplex®SuperBug AmpC assay enabled rapid and reliable detection of pAmpC-encoding genes in Enterobacterales like Klebsiella spp. and Proteus spp. and the distinction between plasmid-mediated and chromosomally encoded AmpC in E. coli.


Subject(s)
Bacterial Proteins , Plasmids , Whole Genome Sequencing , beta-Lactamases , beta-Lactamases/genetics , Plasmids/genetics , Whole Genome Sequencing/methods , Bacterial Proteins/genetics , Humans , Escherichia coli/genetics , Escherichia coli/isolation & purification , Enterobacteriaceae/genetics , Enterobacteriaceae/isolation & purification , Enterobacteriaceae/enzymology , Anti-Bacterial Agents/pharmacology , Microbial Sensitivity Tests , Nucleic Acid Amplification Techniques/methods
2.
J Microbiol Methods ; 135: 66-68, 2017 04.
Article in English | MEDLINE | ID: mdl-28131671

ABSTRACT

We evaluated RAPIDEC® CARBA NP, Neo-Rapid CARB, chromID® CARBA SMART (CARB/OXA), Brilliance™ CRE/ESBL, ChromArt CRE and BBL™ CHROMagar™ CPE for the detection of carbapenemase-producing bacteria. The analytical sensitivity of RAPIDEC® CARBA NP was better than that of Neo-Rapid CARB. A combination of carbapenemase and ESBL screening plates could be advantageous.


Subject(s)
Bacterial Proteins/analysis , Bacteriological Techniques/instrumentation , Bacteriological Techniques/methods , Gram-Negative Bacteria/enzymology , Gram-Negative Bacterial Infections/diagnosis , beta-Lactamases/analysis , Chromogenic Compounds , Colorimetry/methods , Culture Media/chemistry , Gram-Negative Bacteria/classification , Gram-Negative Bacteria/growth & development , Gram-Negative Bacterial Infections/microbiology , Humans , Reagent Kits, Diagnostic , Sensitivity and Specificity , Time Factors
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