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Updated: Dec 11, 2025

Testing the Role of Multicopy Plasmids in the Evolution of Antibiotic Resistance
Published on: May 2, 2018
Tracking of Antibiotic Resistance Transfer and Rapid Plasmid Evolution in a Hospital Setting by Nanopore Sequencing
Silke Peter1,2, Mattia Bosio3,4, Caspar Gross5
1Institute of Medical Microbiology and Hygiene, University of Tübingen, Tübingen, Germany silke.peter@med.uni-tuebingen.de stephan.ossowski@med.uni-tuebingen.de.
Abstract:
Infections with multidrug-resistant bacteria often leave limited or no treatment options. The transfer of antimicrobial resistance genes (ARG) carrying plasmids between bacterial species by horizontal gene transfer represents an important mode of expansion of ARGs. Here, we demonstrate the application of Nanopore sequencing in a hospital setting for monitoring transfer and rapid evolution of antibiotic resistance plasmids within and across multiple species. In 2009, we experienced an outbreak with extensively multidrug-resistant Pseudomonas aeruginosa harboring the carbapenemase-encoding blaIMP-8 gene. In 2012, the first Citrobacter freundii and Citrobacter cronae strains harboring the same gene were detected. Using Nanopore and Illumina sequencing, we conducted comparative analysis of all blaIMP-8 bacteria isolated in our hospital over a 6-year period (n = 54). We developed the computational platform plasmIDent for Nanopore-based characterization of clinical isolates and monitoring of ARG transfer, comprising de novo assembly of genomes and plasmids, plasmid circularization, ARG annotation, comparative genome analysis of multiple isolates, and visualization of results. Using plasmIDent, we identified a 40-kb plasmid carrying blaIMP-8 in P. aeruginosa and C. freundii, verifying the plasmid transfer. Within C. freundii, the plasmid underwent further evolution and plasmid fusion, resulting in a 164-kb megaplasmid, which was transferred to C. cronae Multiple rearrangements of the multidrug resistance gene cassette were detected in P. aeruginosa, including deletions and translocations of complete ARGs. In summary, plasmid transfer, plasmid fusion, and rearrangement of the ARG cassette mediated the rapid evolution of opportunistic pathogens in our hospital. We demonstrated the feasibility of near-real-time monitoring of plasmid evolution and ARG transfer in clinical settings, enabling successful countermeasures to contain plasmid-mediated outbreaks.IMPORTANCE Infections with multidrug-resistant bacteria represent a major threat to global health. While the spread of multidrug-resistant bacterial clones is frequently studied in the hospital setting, surveillance of the transfer of mobile genetic elements between different bacterial species was difficult until recent advances in sequencing technologies. Nanopore sequencing technology was applied to track antimicrobial gene transfer in a long-term outbreak of multidrug-resistant Pseudomonas aeruginosa, Citrobacter freundii, and Citrobacter cronae in a German hospital over 6 years. We developed a novel computational pipeline, pathoLogic, which enables de novo assembly of genomes and plasmids, antimicrobial resistance gene annotation and visualization, and comparative analysis. Applying this approach, we detected plasmid transfer between different bacterial species as well as plasmid fusion and frequent rearrangements of the antimicrobial resistance gene cassette. This study demonstrated the feasibility of near-real-time tracking of plasmid-based antimicrobial resistance gene transfer in hospitals, enabling countermeasures to contain plasmid-mediated outbreaks.
Insights
Nanopore sequencing tracked antimicrobial resistance gene transfer and plasmid evolution in a German hospital over six years. This technology enables near-real-time monitoring to contain multidrug-resistant bacterial outbreaks.
Area of Science:
- Microbiology
- Genomics
- Infectious Diseases
Background:
- Multidrug-resistant bacteria pose a significant global health threat.
- Horizontal gene transfer of antimicrobial resistance genes (ARG) via plasmids accelerates resistance spread.
- Monitoring ARG transfer between bacterial species is crucial for infection control.
Purpose of the Study:
- To apply Nanopore sequencing for monitoring ARG plasmid transfer and evolution in a hospital setting.
- To develop a computational platform for analyzing clinical isolates and tracking ARG transfer.
- To investigate a 6-year outbreak involving multidrug-resistant *Pseudomonas aeruginosa*, *Citrobacter freundii*, and *Citrobacter cronae*.
Main Methods:
- Utilized Nanopore and Illumina sequencing for comparative analysis of 54 *bla*IMP-8-positive bacterial isolates.
- Developed the *plasmIDent* computational platform for *de novo* genome and plasmid assembly, ARG annotation, and comparative analysis.
- Analyzed plasmid transfer, fusion, and rearrangement events over a 6-year period.
Main Results:
- Verified plasmid transfer of *bla*IMP-8 between *P. aeruginosa* and *C. freundii* via a 40-kb plasmid.
- Observed plasmid fusion within *C. freundii* to form a 164-kb megaplasmid, subsequently transferred to *C. cronae*.
- Detected multiple rearrangements of ARG cassettes in *P. aeruginosa*, including deletions and translocations.
Conclusions:
- Plasmid transfer, fusion, and ARG cassette rearrangement drive rapid evolution of opportunistic pathogens.
- Nanopore sequencing enables near-real-time monitoring of plasmid evolution and ARG transfer in clinical settings.
- This approach facilitates effective countermeasures against plasmid-mediated outbreaks.
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