In vitro activity of colistin sulfate against Enterobacteriaceae producing extended-spectrum β-lactamases

J Microbiol Immunol Infect. 2015 Dec;48(6):699-702. doi: 10.1016/j.jmii.2013.11.005. Epub 2013 Dec 30.

Abstract

The widespread multidrug-resistant Enterobacteriaceae pose a serious therapeutic challenge. Colistin and tigecycline are potential antimicrobial agents for treating infections caused by extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae. We evaluated the in-vitro activity of colistin sulfate against 253 ESBL producers isolated from patients admitted to a medical center in southern Taiwan (Escherichia coli, n = 82; Klebsiella pneumoniae, n = 102; Enterobacter cloacae, n = 34; and Serratia marcescens, n = 35). Colistin showed promising in-vitro activity against E. coli, K. pneumoniae, and E. cloacae, but not S. marcescens. One ESBL-producing K. pneumoniae strain with resistance to carbapenems (ertapenem, imipenem, and meropenem) was selected for time-killing studies. A combination of colistin and tigecycline showed synergism, but there was an inoculum effect. In conclusion, colistin was active against most ESBL-producing Enterobacteriaceae, and a combination of colistin with tigecycline was synergistic against some highly resistant strains, even those with carbapenem resistance.

Keywords: Colistin; ESBL; Enterobacteriaceae; Tigecycline.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / pharmacology*
  • Colistin / pharmacology*
  • Enterobacter cloacae / drug effects*
  • Enterobacter cloacae / isolation & purification
  • Enterobacter cloacae / metabolism
  • Enterobacteriaceae Infections / drug therapy
  • Escherichia coli / drug effects*
  • Escherichia coli / isolation & purification
  • Escherichia coli / metabolism
  • Humans
  • Klebsiella pneumoniae / drug effects*
  • Klebsiella pneumoniae / isolation & purification
  • Klebsiella pneumoniae / metabolism
  • Microbial Sensitivity Tests
  • Minocycline / analogs & derivatives
  • Minocycline / pharmacology
  • Serratia marcescens / drug effects*
  • Serratia marcescens / isolation & purification
  • Serratia marcescens / metabolism
  • Tigecycline
  • beta-Lactamases / biosynthesis
  • beta-Lactamases / genetics*

Substances

  • Anti-Bacterial Agents
  • Tigecycline
  • beta-Lactamases
  • Minocycline
  • Colistin