4.6 Article

Ceftazidime-Avibactam Resistance in Klebsiella pneumoniae Sequence Type II Due to a Mutation in Plasmid-Borne blakpc-2 to blakpc-33, in Henan, China

Journal

INFECTION AND DRUG RESISTANCE
Volume 14, Issue -, Pages 1725-1731

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IDR.S306095

Keywords

ceftazidime-avibactam; drug resistance; carbapenem-resistant Klebsiella pneumoniae; K. pneumoniae carbapenemase-2; ST11

Funding

  1. Science and Technology Research Project of Henan Province [SBGJ2018084]

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The study demonstrated the evolution of ceftazidime-avibactam resistance in carbapenem-resistant Klebsiella pneumoniae (CRKP) isolated from a patient undergoing CZA treatment. The research revealed that after 6 days of CZA treatment, the CRKP strains exhibited mutations that led to decreased susceptibility to CZA.
Purpose: Carbapenem-resistant Klebsiella pneumoniae (CRKP) represents a serious problem worldwide. Herein, we describe the evolution of ceftazidime-avibactam (CZA) resistance by sequencing clinical isolates from a patient with CRKP infection undergoing CZA treatment. Patients and Methods: In this study, six CRKP strains were isolated from sputum and blood samples of a patient with CRKP infection after intracerebral hemorrhage. Two strains were selected for whole-genome analysis. Results: Drug susceptibility testing showed that the MIC of CZA for CRKP strains isolated after 6 days of CZA treatment was 64-fold higher than that for three CRKP strains isolated before CZA treatment (4 vs >256 mu g/mL), whereas the MIC of imipenem and meropenem was 128-fold (>32 vs 0.25 mu g/mL) and 16-fold (> 32 vs 2 mu g/mL) lower relatively, respectively. Multilocus sequence typing showed that all six CRKP strains isolated from the patient were ST11 and pulsed-field gel electrophoresis confirmed that they were of the same clone. Two strains were selected for whole-genome analysis. The aspartic acid residue at position 179 in the Omega loop was replaced by a tyrosine residue in the resistant strain, and the plasmid carried a bla(KPC-2) to bla(KPC-33) mutation. The results of the modified carbapenem inactivation method and the carbapenemase inhibitor enhancement and colloidal gold enzyme immunochromatographic assays for bla(KPC-33) were negative. Conclusion: This is the first report from Henan to show that treatment with CZA for 6 days can cause mutations and change the phenotype from CZA sensitive to resistant. Therefore, routine testing for drug susceptibility and carbapenemase phenotypes should be conducted during treatment with CZA, and genotype determination is essential.

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