Contribution of β-lactamases and porin proteins OmpK35 and OmpK36 to carbapenem resistance in clinical isolates of KPC-2-producing Klebsiella pneumoniae.

نویسندگان

  • Ying Zhang
  • Xiaofei Jiang
  • Yanyan Wang
  • Gang Li
  • Yueru Tian
  • Hong Liu
  • Fuqi Ai
  • Yiming Ma
  • Bei Wang
  • Feiyi Ruan
  • Kumar Rajakumar
چکیده

Fifty-seven carbapenem-resistant Klebsiella pneumoniae isolates belonging to ST11 (50 isolates), ST423 (5 isolates), and two other sequence types were studied. All were positive for blaKPC-2, blaTEM-1, and blaCTX-M-14. SDS-PAGE analysis of six representative isolates demonstrated varied porin expression. Nevertheless, when blaKPC-2 was deleted, carbapenem resistance was markedly reduced. Additionally, SHV-12, DHA-1, and/or VIM-1 appeared to contribute to accessory carbapenemase activity. In contrast, OmpK35 and/or OmpK36 deficiency seemed to serve only as a minor cooperative factor.

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عنوان ژورنال:
  • Antimicrobial agents and chemotherapy

دوره 58 2  شماره 

صفحات  -

تاریخ انتشار 2014