4.4 Article

Mechanisms of Ceftazidime and Ciprofloxacin Transport through Porins in Multidrug-Resistance Developed by Extended-Spectrum Beta-Lactamase E.coli Strains

Journal

JOURNAL OF FLUORESCENCE
Volume 21, Issue 4, Pages 1421-1429

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10895-010-0826-7

Keywords

Outer membrane porins; Ceftazidime; Ciprofloxacin; Non-fluorescent complex; Extended-spectrum beta-lactamase E.coli strain

Funding

  1. Romanian Ministry of Research [CEEX 2-Cex-06-11-49/2006, CEEX 168/2006]

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Resistance towards antibiotics stands out today as a major issue in the clinical act of treatment of bacterial-generated infections. This process was characterized in proteoliposomes reconstituted from an E.coli strain isolated from invasive infections (blood culture) occurred in patients with a cardio-vascular device admitted for surgery. Fluorescence spectroscopy and patch-clamp technique have been used. Two types of antibiotics have been targeted: ceftazidime and ciprofloxacin. Antibiotics addition in proteoliposomes suspension undergoes a quenching in tryptophan residues from outer membrane porins structure, probably due to the formation of a transient non-fluorescent porin-antibiotic complex. Patch-clamp recordings revealed strong ion current blockages for both antibiotics, reflecting antibiotic-channel interactions but with varying strength of interaction. The present study puts forward the mechanism of multidrug-resistance in extended-spectrum beta-lactamase E.coli strains, as being caused by alterations of the antibiotics transport across the porins of the outer bacterial membrane.

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