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Related Experiment Video

Updated: Jun 16, 2026

Anti-virulent Disruption of Pathogenic Biofilms using Engineered Quorum-quenching Lactonases
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Resonant activation: a strategy against bacterial persistence.

Yan Fu1, Meng Zhu, Jianhua Xing

  • 1Interdisciplinary Program of Genetics, Bioinformatics, and Computational Biology, Virginia Polytechnic Institute and State University, Blacksburg, VA 24060, USA.

Physical Biology
|February 12, 2010
PubMed
Summary

Persister cells cause antibiotic resistance by remaining dormant. This study shows resonant activation (RA) can trigger these cells to become susceptible to antibiotics, reducing treatment time and drug dosage.

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Area of Science:

  • Microbiology
  • Biophysics
  • Mathematical Biology

Background:

  • Persister cells are a subpopulation of bacteria that survive antibiotic treatment due to their dormant state.
  • This dormancy leads to significant challenges in eradicating bacterial infections and contributes to antimicrobial drug resistance.
  • Current treatments struggle to effectively eliminate these resilient persister cells.

Purpose of the Study:

  • To introduce a novel strategy for eliminating persister cells by inducing their transition to a drug-sensitive state.
  • To investigate the application of resonant activation (RA) as a mechanism to achieve fast and synchronized phenotypic switching in bacteria.
  • To demonstrate the potential of RA in enhancing the efficacy of antibiotic treatments against bacterial populations.

Main Methods:

  • Utilized stochastic Gillespie simulations to model the phenotypic switching dynamics of a single bacterium using a generic toggle switch model.
  • Investigated the phenomenon of resonant activation (RA) as a means to facilitate synchronized barrier crossings in biological systems.
  • Employed coupled single-cell and population-level simulations to assess the impact of RA on bacterial sterilization.

Main Results:

  • Demonstrated the existence and efficacy of resonant activation in driving the phenotypic switching of individual bacterial cells.
  • Showcased that RA significantly reduces the time required to sterilize bacterial populations.
  • Quantified the reduction in the total amount of antibiotics needed for effective bacterial eradication when using the RA strategy.

Conclusions:

  • Resonant activation is a viable and effective strategy for targeting and eliminating antibiotic-resistant persister cells.
  • The RA-based approach offers a promising method to enhance antibiotic therapy by increasing bacterial cell susceptibility.
  • The principles of resonant activation may be applicable to other biological transitions, including potential applications in cancer therapy.