Proteomic study in an Escherichia coli strain from seagulls of the Berlengas Natural Reserve of Portugal

DOI: 10.5584/jiomics.v1i1.19

Authors

  • Luís Pinto Department of Genetics and Biotechnology, University of Trás-os-Montes and Alto Douro, Vila Real, Portugal
  • Patrícia Poeta Veterinary Science Department, University of Trás-os-Montes and Alto Douro, Vila Real, Portugal
  • Hajer Radhouani Department of Genetics and Biotechnology, University of Trás-os-Montes and Alto Douro, Vila Real, Portugal
  • Céline Coelho Department of Genetics and Biotechnology, University of Trás-os-Montes and Alto Douro, Vila Real, Portugal
  • Carlos Carvalho Department of Genetics and Biotechnology, University of Trás-os-Montes and Alto Douro, Vila Real, Portugal
  • Jorge Rodrigues Centre of Studies of Animal and Veterinary Sciences, University of Trás-os-Montes and Alto Douro, Vila Real, Portugal
  • Carmen Torres Biochemistry and Molecular Biology Area, University of Rioja, Logroño, Spain
  • Rui Vitorino Chemistry Department, University of Aveiro, Aveiro, Portugal
  • Pedro Domingues Chemistry Department, University of Aveiro, Aveiro, Portugal
  • Gilberto Igrejas Department of Genetics and Biotechnology, Institute for Biotechnology and Bioengineering, Centre of Genetics and Biotechnology, University of Trás-os-Montes and Alto Douro, Vila Real, Portugal

Abstract

The increasing bacterial resistance among common pathogens is threatening theeffectiveness of several antibiotics. This represents a serious public health problem as such bacterial strains have already been detected in domestic, wild-life animals and humans. Using Escherichia coli as a model organism, we applied a proteomic approach to the topic of antimicrobial resistance. In order to identify and characterize the proteome of extended-spectrum β-lactamase (ESBL) type TEM-52 producing-Escherichia coli strain of a faecal sample taken from Yellow-legged seagulls (Larus cachinnans) a bidimensional electrophoresis (2-DE) technique with an isoelectric focusing followed by a SDS-PAGE, was used. Eighty seven individualized protein spots were identified. All were suitable for peptide mass fingerprinting by a mass spectrometric technique (MALDI/TOF MS). Their identification was carried out by searching appropriate bioinformatic databases. All proteins were related to E. colistrains. Detection of proteins related to several E. coli strains linked with virulent and enterohaemorrhagic consequences in ESBL producing-E. coli isolates of seagull samples raises the question of how such similarities arise bearing in mind these remarkably different microbial ecosystems.

Published

2011-04-14