4.7 Article

Hijacking a small plasmid to confer high-level resistance to aztreonam-avibactam and ceftazidime-avibactam

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ELSEVIER
DOI: 10.1016/j.ijantimicag.2023.106985

Keywords

Multi-copy plasmids; Small plasmids; Aztreonam; Avibactam; Enterobacterales; Carbapenem resistance; IS 1294; Antimicrobial resistance; Fitness cost

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This study found that mobile genetic elements carrying antimicrobial resistance genes can hijack small plasmids, enhancing bacteria's ability to resist antibiotics. It also found that the presence of multi-copy small plasmids and pre-existing resistance genes on plasmids have different effects on bacteria's resistance.
Acquired /3-lactamase-encoding genes are typically carried by large plasmids in Gram-negative bacteria, which also commonly carry multi-copy small plasmids. This study found that mobile genetic elements carrying antimicrobial resistance genes are capable of hijacking small plasmids. This study focused on aztreonam-avibactam (ATM-AVI) as this combination can be used to effectively counter almost all /3- lactamases produced by bacteria, and has been recommended against carbapenem-resistant Enterobac-terales. A clinical strain (085003) of carbapenem-resistant Escherichia coli was investigated, and mutants (0850 03R32 and 0850 03R512) able to grow under 32/4 and 512/4 mg/L of ATM-AVI were obtained as rep-resentatives of low-and high-level resistance, respectively, by induction. Comparative genomics showed that 085003R32 and 085003R512 had a single nucleotide mutation of /3-lactamase gene blaCMY-2, encod-ing a novel CMY with a Thr319Ile substitution, assigned 'CMY-2R'. Cloning and enzyme kinetics were used to verify that CMY-2R conferred ATM-AVI resistance by compromising binding of AVI and subse-quent protection of ATM. Mechanisms for the discrepant resistance between 085003R32 and 085003R512 were investigated. Three tandem copies of blaCMY-2R were identified on a self-transmissible IncP1 plasmid of 085003R32 due to IS1294 misrecognizing its end terIS and rolling-circle replication. 085003R512 had only a single copy of blaCMY-2R on the IncP1 plasmid, but possessed anther blaCMY-2R on an already present 4-kb small plasmid. IS1294-mediated mobilization on to this multi-copy small plasmid increased the copy number of blaCMY-2R significantly, rendering higher resistance. This study shows that bacteria can employ multiple approaches to accommodate selection pressures imposed by exposure to varied concentrations of antimicrobial agents.(c) 2023 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights reserved.

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