4.3 Article

Risk factors for KPC-producing Klebsiella pneumoniae: watch out for surgery

Journal

JOURNAL OF MEDICAL MICROBIOLOGY
Volume 65, Issue -, Pages 547-553

Publisher

MICROBIOLOGY SOC
DOI: 10.1099/jmm.0.000254

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Funding

  1. Brazilian National Research Council (CNPq) [480949/2013-1]
  2. Support Foundation for the Development of Education, Science and Technology in the State of Mato Grosso do Sul (FUNDECT) [05/2011, 04/2012]
  3. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)
  4. AstraZeneca
  5. MSD
  6. Novartis
  7. Thermo Fisher Scientific
  8. bioMerieux

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This study describes the molecular characteristics and risk factors associated with carbapenem-resistant Klebsiella pneumoniae strains. Risk factors associated with KPC-producing K pneumoniae strains were investigated in this case -control study from May 2011 to May 2013. Bacterial identification was performed by matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry (MALDI-TOF MS). Antimicrobial susceptibility was determined by broth microdilution. Carbapenemase production was assessed by both modified Hodge test (MHT) and ertapenem hydrolysis using MALDI-TOF MS. The presence of beta-lactamase-encoding genes was evaluated by PCR and DNA sequencing. Alterations in genes encoding K. pneumoniae outer membrane proteins were analysed by PCR and DNA sequencing as well as SDS-PAGE. Genetic relatedness among strains was determined by pulsed-field gel electrophoresis. This study included 94 patients. Longer hospitalisation, mechanical ventilation, catheters, and previous surgery were associated with KPC-producing K. pneumoniae. Sixty-eight strains showed resistance to carbapenems. Carbapenemase production was detected by MHT in 67 K pneumoniae strains and by MALDI-TOF MS in 57. The presence of the bla(KPC-.2) gene was identified in 57 strains. The bla(KPC-.2) gene was not found in 11 carbapenem-resistant K pneumoniae; instead, the bla(CTX-M-1-like), bla(CTX-M-8 like), bla(CTX-M-14-like) and bla(SHV-like) genes associated with OmpK35 and OmpK36 alterations were observed. Thirty-three KPC-producing K pneumoniae strains were clonally related, and patients infected with these strains had a higher mortality rate (78.78 %). Our results show that KPC-producing K pneumoniae was associated with several healthcare-related risk factors, including recent surgery.

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