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.

Msphere
|August 21, 2020
PubMed

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.