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Exploring the effect of sequential antibiotic exposure in resistant Escherichia coli causing urinary tract infections: a proof of principle study.

Lisa Göpel, Laura Kirchhoff, Olivia Gopleac, Leif Tüeffers, Susanne Hauswaldt, Sébastien Boutin, Jan Rupp, Dennis Nurjadi

Abstract

UNLABELLED: Antimicrobial resistance development, particularly in infections such as urinary tract infections (UTIs), is a global clinical concern. The objective of this study was to determine if sequential antibiotic exposure with ciprofloxacin and mecillinam can reduce the growth of resistant clinical Escherichia coli strains, thus improving the effectiveness of antibiotic therapy. Six E. coli isolates with heterogeneous resistance to ciprofloxacin and/or mecillinam obtained from patients with UTIs were exposed to one of the antibiotics (0.75 × minimum inhibitory concentration, MIC) for 1 h. This was followed by treatment with the second antibiotic at different concentrations (0.0375/0.075/0.375/0.75 × MIC). Continuous growth measurements were conducted in order to assess the impact of sequential exposure. One representative strain was selected for intact cell counting. In addition, a checkerboard assay was conducted to investigate the synergistic impact of ciprofloxacin and mecillinam, and genetic analyses were performed to identify the mechanisms of resistance for all isolates. The six E. coli strains were phylogenetically different, and none exhibited a synergistic effect for ciprofloxacin and mecillinam. Our data suggest that sequential exposure to mecillinam and ciprofloxacin appears to reduce the growth capacity of clinical E. coli isolates with phenotypic resistance to either or both agents. Sequential antibiotic exposure may be an interesting strategy to improve the antibiotic efficacy of current agents to overcome phenotypic resistance in E. coli.

IMPORTANCE: As global rates of antibiotic resistance increase and the development of new antibiotics become more difficult and costly, it is important to explore alternative strategies to improve the effectiveness of existing antibiotics. Previous studies have shown that sequential exposure of Pseudomonas aeruginosa to two antibiotics can effectively kill the bacteria and reduce the likelihood of resistance developing. However, the potential of this sequential approach for the treatment of Escherichia coli infections has not been thoroughly investigated. In our study, we conducted a proof-of-principle study to determine whether sequential exposure to mecillinam and ciprofloxacin can overcome phenotypic resistance to one or both drugs. We found that when E. coli were treated with subinhibitory doses of mecillinam followed by ciprofloxacin, their growth was significantly inhibited compared to treatment with ciprofloxacin alone, suggesting that sequential antibiotic exposure may be a viable strategy for treating infections caused by resistant E. coli.

Original languageEnglish
Article numbere02525-24
JournalMicrobiology Spectrum
Volume13
Issue number3
Pages (from-to)e0252524
ISSN2165-0497
Publication statusPublished - 04.03.2025

Funding

FundersFunder number
German Science Foundation within the Excellence cluster Precision Medicine in chronic Inflammation
Deutsche Forschungsgemeinschaft
Philip Morris InternationalEXC 2167-390884018
Bundesministerium für Bildung und ForschungTTU 08.824

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being
    2. SDG 6 - Clean Water and Sanitation
      SDG 6 Clean Water and Sanitation

    Research Areas and Centers

    • Academic Focus: Center for Infection and Inflammation Research (ZIEL)

    DFG Research Classification Scheme

    • 2.22-31 Clinical Infectiology and Tropical Medicine
    • 2.21-03 Medical Microbiology and Mycology, Hygiene, Molecular Infection Biology
    • 2.21-05 Immunology

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    • EXC 2167: Precision Medicine in Chronic Inflammation (PMI)

      Schreiber, S. (Speaker), Baines, J. F. (Project Staff), Bosch, T. C. G. (Project Staff), Buyx, A. (Project Staff), Erdmann, J. (Project Staff), Franke, A. (Project Staff), Huber, R. (Project Staff), Klein, C. (Project Staff), Köhl, J. (Project Staff), König, I. R. (Project Staff), Lange, C. (Project Staff), Laudes, M. (Project Staff), Lieb, W. (Project Staff), Ludwig, R. (Project Staff), Nebel, A. (Project Staff), Niemann, S. (Speaker), Rabe, K. F. (Project Staff), Riemekasten, G. (Speaker), Rose-John, S. (Project Staff), Rosenstiel, P. C. (Project Staff), Schulenburg, H. (Project Staff), Schwarz, K. (Project Staff), Traulsen, A. (Project Staff), Weidinger, S. (Project Staff) & Zillikens, D. (Project Staff)

      01.01.1931.12.32

      Project: DFG Joint ResearchCluster of Excellence

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