4.7 Article

Phenotypic, Biochemical, and Genetic Analysis of KPC-41, a KPC-3 Variant Conferring Resistance to Ceftazidime-Avibactam and Exhibiting Reduced Carbapenemase Activity

Journal

ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
Volume 63, Issue 12, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.01111-19

Keywords

KPC; ceftazidime-avibactam; Klebsiella pneumoniae

Funding

  1. University of Fribourg, Switzerland
  2. Swiss National Science Foundation [FNS-31003A_163432]

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A novel KPC variant, KPC-41, was identified in a Klebsielia pneumoniae clinical isolate from Switzerland. This beta-lactamase possessed a 3-amino-acid insertion (Pro-Asn-Lys) located between amino acids 269 and 270 compared to the KPC-3 amino acid sequence. Cloning and expression of the bla(KPC-41) gene in Escherichia coli, followed by determination of MIC values and kinetic parameters, showed that KPC-41, compared to those of KPC-3, has an increased affinity to ceftazidime and a decreased sensitivity to avibactam, leading to resistance to ceftazidime-avibactam once produced in K. pneumoniae. Furthermore, KPC-41 exhibited a drastic decrease of its carbapenemase activity. This report highlights that a diversity of KPC variants conferring resistance to ceftazidime-avibactam already circulate in Europe.

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