4.7 Article

Cross-resistance to cefiderocol and ceftazidime-avibactam in KPC β-lactamase mutants and the inoculum effect

Journal

CLINICAL MICROBIOLOGY AND INFECTION
Volume 27, Issue 8, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.cmi.2021.04.016

Keywords

Cefiderocol resistance; Ceftazidime-avibactam resistance; Cross-resistance; Inoculum effect; KPC beta-lactamases; KPC-2; KPC-3; KPC-31

Funding

  1. ARC Foundation [DOC20190509066]

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This study reveals that CZA-resistant KPC variants may lead to cross-resistance to cefiderocol by increasing the MICs. Additionally, cefiderocol is greatly impacted by the inoculum effect, indicating precautions should be taken when treating infections with suspected high inoculum levels.
Objectives: Ceftazidime-avibactam (CZA) and cefiderocol are recently commercialized molecules active against highly drug-resistant bacteria, including carbapenem-resistant members of the Enterobacteriaceae. Mutants resistant to CZA have been described, notably in Klebsiella pneumoniae carbapenemase (KPC) producers. Considering the structural similarities between ceftazidime and cefiderocol, we hypothesized that resistance to CZA in KPC-producing members of the Enterobacterales may lead to cross-resistance to cefiderocol. Methods: CZA-resistant mutants from three clinical isolates of the Enterobacterales carrying either bla(KPC-2) or bla(KPC-3) were selected in vitro. Mutants with increased MIC to CZA compared to the ancestral allele were cloned in a pBR322 plasmid and expressed in Escherichia coli TOP10. We evaluated the impact of these mutations on cefiderocol MICs and minimal bactericidal concentrations (MBCs), and we assessed the impact of bacterial inoculum size on cefiderocol MICs. Results: We used 37 KPC mutants with increased CZA MICs. Of these, six have been described previously in clinical isolates. Compared to the wild-type alleles, increases in the cefiderocol MICs of 4- to 32-fold were observed for 75.6% of tested mutants (28/37), MICs reaching up to 4 mg/L in E. coli TOP10 for KPC-31 (D179Y-H274Y mutations). MBCs and MICs of cefiderocol were similar, confirming the bactericidal activity of this drug. Finally, when using higher inocula (10(7) CFU/mL), a large increase in cefiderocol MIC was observed, and all isolates were categorized as resistant. Conclusion: We observed that most of the CZA-resistant KPC variants have a possible impact on cefiderocol by increasing the cefiderocol MICs. In addition, cefiderocol is greatly impacted by the inoculum effect, suggesting that precautions should be taken when treating infections with a suspected high inoculum. (C) 2021 The Authors. Published by Elsevier Ltd on behalf of European Society of Clinical Microbiology and Infectious Diseases.

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