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Mutations in blaKPC-3 That Confer Ceftazidime-Avibactam Resistance Encode Novel KPC-3 Variants That Function as Extended-Spectrum β-Lactamases.

Ghady HaidarCornelius J ClancyRyan K ShieldsBinghua HaoShaoji ChengM Hong Nguyen
Published in: Antimicrobial agents and chemotherapy (2017)
We identified four blaKPC-3 mutations in ceftazidime-avibactam-resistant clinical Klebsiella pneumoniae isolates, corresponding to D179Y, T243M, D179Y/T243M, and EL165-166 KPC-3 variants. Using site-directed mutagenesis and transforming vectors into Escherichia coli, we conclusively demonstrated that mutant blaKPC-3 encoded enzymes that functioned as extended-spectrum β-lactamases; mutations directly conferred higher MICs of ceftazidime-avibactam and decreased the MICs of carbapenems and other β-lactams. Impact was strongest for the D179Y mutant, highlighting the importance of the KPC Ω-loop.
Keyphrases
  • klebsiella pneumoniae
  • escherichia coli
  • multidrug resistant
  • gram negative
  • copy number
  • crispr cas
  • wild type
  • transcription factor
  • biofilm formation
  • staphylococcus aureus
  • dna methylation