| Literature DB >> 32988825 |
Mustafa Sadek1, Mario Juhas1, Laurent Poirel2,3,4, Patrice Nordmann1,3,4.
Abstract
Metallo-β-lactamase (MBL)-producing Escherichia coli isolates resistant to the newly developed β-lactam/β-lactamase inhibitor drug combination aztreonam-avibactam (ATM-AVI) have been reported. Here, we analyzed a series of 118 clinical MBL-producing E. coli isolates of various geographical origins for susceptibility to ATM-AVI. The nature of the PBP3 protein sequence and the occurrence of bla CMY genes for susceptibility to ATM-AVI were investigated. We showed here that elevated MICs of ATM-AVI among MBL-producing E. coli isolates resulted from a combination of different features, including modification of PBP3 protein sequence through specific amino acid insertions and production of CMY-type enzymes, particularly, CMY-42. We showed here that those insertions identified in the PBP3 sequence are not considered the unique basis of resistance to ATM-AVI, but they significantly contribute to it.Entities:
Keywords: CMY-42; Escherichia coli; NDM; PBP3; aztreonam-avibactam; metallo-β-lactamase
Year: 2020 PMID: 32988825 PMCID: PMC7674043 DOI: 10.1128/AAC.01659-20
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191