Enteroaggregative Escherichia coli: Surface protein dispersin increases bacterial uptake of ciprofloxacin

Ninell P. Mortensen, Nadia Boisen, Sonia Carey, Stephen J. Kennel, Jason D. Fowlkes, Mitchel J. Doktycz, James P. Nataro, David P. Allison

Research output: Contribution to journalArticlepeer-review

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Abstract

Enteroaggregative Escherichia coli (EAEC) causes diarrhoea. The antibiotic of choice for treating EAEC infections is ciprofloxacin. EAEC differs from other subgroups of pathogenic E. Coli by having a surface protein, dispersin, which has previously been shown to play an important role in ciprofloxacin susceptibility for EAEC model strain 042. To investigate further the role of dispersin in ciprofloxacin susceptibility, minimum inhibitory concentrations (MICs) were determined for 25 clinical isolates, including 15 with dispersin and 10 without. Dispersin-positive strains had a lower MIC than dispersin-negative strains. The mechanism of action behind this observation may be caused by dispersin (i) increasing the bacteria-antibiotic interaction or (ii) facilitating ciprofloxacin access to the intracellular target, DNA gyrase/topoisomerase. To test the role of dispersin in ciprofloxacin sensitivity, EAEC 042 as well as its isogenic mutants, dispersin mutant (042aap) and a mutant in the transporter apparatus gene aatA, believed to be involved in dispersin transport to the bacterial surface (042aatA), were utilised. As predicted, 042 had a higher sensitivity to ciprofloxacin than 042aap, but it was also found that the MIC of 042aatA was similar to 042aap. To address the question of the role of dispersin in ciprofloxacin susceptibility, the concentration of ciprofloxacin bound in biofilms of 042 and 042aap was quantified by treating bacteria with radiolabelled 2-14C- ciprofloxacin. The results showed that dispersin did not increase the amount of bound ciprofloxacin as a function of biomass, indicating instead that dispersin facilitates ciprofloxacin access to the intracellular target leading to increased antibiotic susceptibility.

Original languageEnglish
Pages (from-to)462-465
Number of pages4
JournalInternational Journal of Antimicrobial Agents
Volume42
Issue number5
DOIs
StatePublished - Nov 2013

Funding

The authors thank Dr Waldir Pereira Elias (Laboratory of Bacteriology, Instituto Butantan, São Paulo, Brazil) for bacterial strains C783-12 and C784-12. Oak Ridge National Laboratory is managed by UT-Battelle, LLC, for the US Department of Energy (DOE) under contract no. DEAC05-00OR22725. The authors would also like to acknowledge support from the Center for Nanophase Materials Sciences, which is sponsored at Oak Ridge National Laboratory by the Office of Basic Energy Sciences, DOE. Funding : The authors acknowledge research support from the Department of Energy (DOE) Office of Biological and Environmental Sciences [contract no. DEAC05-00OR22725]. Financial support from Lundbeckfonden, Denmark (to NPM).

Keywords

  • Antibiotic susceptibility
  • Ciprofloxacin
  • Dispersin
  • Enteroaggregative
  • Escherichia coli
  • Radiolabelled

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