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Patterns of resistance associated with integrons, the extended-spectrum beta-lactamase SHV-5 gene, and a multidrug efflux pump of Klebsiella pneumoniae causing a nosocomial outbreak. | LitMetric

AI Article Synopsis

  • A nosocomial outbreak of multiresistant Klebsiella pneumoniae was investigated, revealing varied resistance patterns among patients and a need for improved screening methods.
  • Genetic strain typing via pulsed-field gel electrophoresis confirmed the clonality of outbreak strains and identified at least one missed patient due to inadequate ESBL screening.
  • The presence of the SHV-5 ESBL gene was found in almost all outbreak strains, and correlations between ciprofloxacin and cefoxitin MICs suggested that low-level expression of ESBL genes could evade detection, indicating the need for better screening criteria.

Article Abstract

Multiresistant Klebsiella pneumoniae caused a nosocomial outbreak. Resistance patterns of the presumed outbreak isolates varied among and within patients. In order to control the outbreak, screening for extended-spectrum beta-lactamase (ESBL)-producing K. pneumoniae was commenced. A number of susceptible K. pneumoniae strains were stored to serve as controls in genetic strain typing. Typing by pulsed-field gel electrophoresis proved the clonality of the strains in the recognized outbreak patients. Typing of the control strains by pulsed-field gel electrophoresis showed that at least one patient had been missed by the ESBL screening procedure. Further genetic typing confirmed the presence of the SHV-5 ESBL gene in all but one of the outbreak strains. Variable presence of integrons that carried the aminoglycoside resistance genes aadB and aadA2 was found. A gyrA mutation in codon 83 was present in all outbreak strains tested, despite considerable differences in ciprofloxacin MICs. The MICs of ciprofloxacin and the chemically unrelated drug cefoxitin were correlated (r = 0.86, P < 0.01) and were compatible with the overexpression of an efflux pump in a subset of the outbreak strains. We conclude that outbreak strains that express an ESBL gene only at a low level may pass unnoticed in a screening procedure, when the laboratory is unaware of variable ESBL expression. In this particular outbreak, screening for strains for which ciprofloxacin MICs were > or =0.25 micro g/ml would in retrospect have been the most sensitive method for detection of the K. pneumoniae outbreak strain.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC150252PMC
http://dx.doi.org/10.1128/JCM.41.3.1161-1166.2003DOI Listing

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