Comparative proteomics to evaluate multi drug resistance in Escherichia coli

Mol Biosyst. 2012 Apr;8(4):1060-7. doi: 10.1039/c1mb05385j. Epub 2011 Nov 28.

Abstract

Drug resistance in food-borne bacterial pathogens is an almost inevitable consequence of the use of antimicrobial drugs, used either therapeutically or to avoid infections in food-producing animals. In the past decades, the spread and inappropriate use of antibiotics have caused a considerable increase of antibiotics to which bacteria have developed resistance and, moreover, bacteria are becoming resistant to more than one antibiotic simultaneously. Understanding mechanisms at the molecular level is extremely important to control multi-resistant strains and to develop new therapeutic strategies. In the present study, comparative proteomics was applied to characterize membrane and cytosolic proteome in order to investigate the regulation of protein expression in multi-resistance E. coli isolated from young never vaccinated water buffalo. Results highlighted differentially expressed proteins under multi drug resistance conditions giving new insights about mechanisms involved in resistance, as quorum sensing mechanisms, and suggesting possible novel bacterial targets to develop alternative antibiotic drugs.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Bacterial Typing Techniques
  • Buffaloes
  • Cell Membrane / metabolism
  • Cell Membrane / microbiology
  • Chromatography, High Pressure Liquid
  • Cytosol / metabolism
  • Cytosol / microbiology
  • Drug Resistance, Multiple, Bacterial / genetics*
  • Electrophoresis, Gel, Two-Dimensional / methods
  • Escherichia coli / classification
  • Escherichia coli / drug effects*
  • Escherichia coli / isolation & purification
  • Mass Spectrometry / methods
  • Microbial Sensitivity Tests
  • Proteome / drug effects
  • Proteome / metabolism
  • Proteomics / methods*
  • Tandem Mass Spectrometry

Substances

  • Anti-Bacterial Agents
  • Proteome