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Updated: Jun 14, 2025

Testing the Role of Multicopy Plasmids in the Evolution of Antibiotic Resistance
Published on: May 2, 2018
Plasmid-encoded insertion sequences promote rapid adaptation in clinical enterobacteria
Jorge Sastre-Dominguez1, Javier DelaFuente1, Laura Toribio-Celestino1
1Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
Plasmids like pOXA-48 accelerate bacterial evolution by promoting insertion sequence 1 (IS1) transposition. This mechanism drives adaptation in clinical strains, both in vitro and within patients.
Area of Science:
- Microbiology
- Bacterial Genetics
- Evolutionary Biology
Background:
- Plasmids are key drivers of bacterial evolution, primarily through horizontal gene transfer.
- Their role in intragenomic adaptation and evolution beyond gene transfer is less understood.
- The conjugative plasmid pOXA-48 is prevalent in multidrug-resistant clinical bacteria.
Purpose of the Study:
- To investigate how the pOXA-48 plasmid influences the evolution of multidrug-resistant enterobacteria.
- To explore mechanisms of bacterial adaptation mediated by plasmids beyond horizontal gene transfer.
Main Methods:
- Experimental evolution studies.
- Analysis of bacterial evolution within patients.
- Investigating plasmid-encoded insertion sequence 1 (IS1) transposition dynamics.
Main Results:
- The pOXA-48 plasmid facilitates bacterial evolution via transposition of its encoded IS1 elements.
- IS1-mediated gene inactivation accelerates adaptation rates in vitro and in the gut microbiota.
- A negative feedback loop regulating IS1 transposition based on genomic copy number was identified.
Conclusions:
- Plasmid-mediated IS1 transposition is a significant mechanism for rapid bacterial adaptation.
- This highlights an underappreciated role of plasmids in bacterial evolution.
- Findings are relevant given the abundance of IS elements on bacterial plasmids.
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