iModulon analysis uncovers dynamic responses in Escherichia coli to ampicillin and ciprofloxacin, suggesting new targets for disrupting early adaptations.
The earliest responses of pathogenic bacteria to antibiotics can affect the outcome of an infection. While long-term adaptations have been extensively studied, the immediate transcriptional changes that unfold immediately following antibiotic exposure remain poorly understood. Here, we applied iModulon analysis to time-resolved transcriptomic data from Escherichia coli exposed to subinhibitory concentrations of two antibiotics (ampicillin and ciprofloxacin), capturing transcriptional regulatory changes occurring within the first 30 minutes of exposure. This analysis reveals an integrated, three-phase response: an immediate and sustained primary response that broadly activates stress programs, a transient secondary response that restores redox balance, and a tertiary response that supports long-term survival through metabolic remodeling and antibiotic-specific defenses. These results highlight a coordinated and dynamic regulatory strategy describing how metabolic, redox, and stress responses are integrated to manage the physiological challenges of antibiotic stress. By disentangling these overlapping transcriptional regulatory programs, this work offers a genome-scale understanding of how survival mechanisms unfold during the critical moments following antibiotic exposure. The study opens new directions for investigating early survival mechanisms and the possible identification of new targets to disrupt the initial adaptation process.
No takes yet. Share an insight, caveat, or question.
Yuan et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: