The AmpC phenotype in Norwegian clinical isolates of Escherichia coli is associated with an acquired ISEcp1-like ampC element or hyperproduction of the endogenous AmpC

Objectives: The aim of the study was to examine resistance mechanisms associated with an phenotype in Norwegian clinical isolates of Escherichia coli. Methods: Clinical E. coli isolates ( n = 106) with reduced susceptibility to third- generation without clavulanic acid synergy were collected from 12 Norwegian laboratories from 2003 to Twenty- two isolates with an AmpC phenotype were selected for further characterization by isoelectric focusing, different PCR- based techniques, DNA sequencing, AmpC qRT - PCR, studies and plasmid analyses. Results: The 22 isolates were not clonally related by the PFGE analysis. All isolates expressed a beta-lactamase with a pI of 9.0 - 9.2. Ten isolates contained a blaCMY gene, which was linked to an ISEcp1-like-element in all cases. Twelve isolates had mutations or insertions in the promoter or the regions, leading to increased expression of the chromosomal ampC gene. One of these isolates an ISEc10 element inserted upstream of the chromosomal ampC gene. Conclusions: This is the first molecular study of Norwegian clinical E. coli isolates with an AmpC Resistance was mediated either by expression of blaCMY from acquired ISEcp1-like-bla(CMY), or by mutations or insertions in the chromosomal ampC gene control region leading hyperproduction of the endogenous AmpC enzyme. There was no correlation between the level ampC mRNA and the MICs of cephalosporins.