4.7 Article

Emergence and Recovery of Ceftazidime-avibactam Resistance in blaKPC-33-Harboring Klebsiella pneumoniae Sequence Type 11 Isolates in China

Journal

CLINICAL INFECTIOUS DISEASES
Volume 71, Issue -, Pages S436-S439

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciaa1521

Keywords

Carbapenem-resistant K. pneumoniae; Ceftazidime-avibactam; Meropenem-vaborbactam; bla(KPC-2); bla(KPC-33)

Funding

  1. National Natural Science Foundation of China [81871690, 81902101, 81861138051]
  2. National Mega-project for Innovative Drugs [2019ZX09721001-006-004]
  3. China Antimicrobial Surveillance Network [2020QD049]

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This is the first report of ceftazidime-avibactam resistance caused by the bla(KPC-33) mutation through the D179Y variant during the treatment of bla(KPC-2)-positive Klebsiella pneumoniae-related infections in China. The bla(KPC-33)-containing K. pneumoniae was susceptible to meropenem-vaborbactam, cefepime-zidebactam, tigecycline, and polymyxin B. The bla(KPC-33) gene was located on a 77 551-bp transformable plasmid harboring qnrS1 and bla(LAP-2). Detecting bla(KPC-33)-positive K. pneumoniae clinical strains is important for infection control.

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