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original-paper | 08-September-2020

A Polyclonal Spread Emerged: Characteristics of Carbapenem-Resistant Klebsiella pneumoniae Isolates from the Intensive Care Unit in a Chinese Tertiary Hospital

, IMP – Imipenem, AMC – Amoxicillin/clavulanic acid, FEP – cefepime, MXF – moxifloxacin, ISE – isepamicin, TZP – piperacillin/tazobactam, SCF – cefperazone/sulbactam – MEM, meropenem, TGC – tigecycline, LEV – levofloxacin, AMK – amikacin, CIP – ciprofloxacin, PB – polymyxin B, CAZ/AVI – ceftazidime/avibactam, MH – minocycline, ST – sequence type, NA – not available Antimicrobial susceptibility. The isolates in this study were resistant to nearly all clinically available antimicrobials; more than

ZHENGZHENG WANG, FANGYOU YU, XIAOFEI SHEN, MEILAN LI

Polish Journal of Microbiology, Volume 69 , ISSUE 3, 311–319

Short Communication | 27-September-2017

KPC-2-producing Klebsiella pneumoniae ST11 in a Children’s Hospital in Poland

Four Klebsiella pneumoniae isolates from children hospitalized over 10 months in an intensive care unit in a children’s teaching hospital in Poland were analyzed. All of the isolates belonged to a single pulsotype and sequence type (ST) 11, and produced the KPC-2 carbapenemase and extended-spectrum β-lactamase (ESBL) CTX-M-15. They were resistant to a variety of antimicrobials, and their β-lactam resistance patterns were typical for KPC producers. This is one of few cases of

Monika Machulska, Anna Baraniak, Iwona Żak, Katarzyna Bojarska, Dorota Żabicka, Iwona Sowa-Sierant, Waleria Hryniewicz, Marek Gniadkowski

Polish Journal of Microbiology, Volume 66 , ISSUE 3, 401–404

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