Global emergence of Carbapenem-resistant Hypervirulent Klebsiella pneumoniae driven by an IncFII
Summary
Across thousands of genomes and multiple clinical isolate collections, an IncFII plasmid was identified as a key vehicle enabling convergence of carbapenem resistance and hypervirulence in K. pneumoniae, facilitating global dissemination of CR-hvKp.
Key Findings
- Integrated analysis of 67,631 genomes and multi-center clinical isolates implicated an IncFII plasmid in CR-hvKp emergence.
- IncFII-positive CR-hvKp genomes from 24 countries indicate global dissemination.
- Resistance (carbapenemase) acquisition on hvKp backgrounds underlies convergence of hypervirulence and carbapenem resistance.
Clinical Implications
Genomic surveillance should prioritize detection of IncFII plasmids in K. pneumoniae; infection control and stewardship policies can target plasmid-mediated spread and inform empiric therapy in high-risk settings.
Why It Matters
Pinpointing a specific plasmid backbone as the driver of resistance–virulence convergence provides a tangible surveillance and containment target for AMR programs.
Limitations
- Abstracted data indicate observational genomic associations without direct transmission or fitness experiments.
- Sampling bias in public databases may influence geographic and lineage representation.
Future Directions
Prospective genomic surveillance tracking IncFII plasmid movement, functional studies of transfer dynamics and fitness costs, and targeted infection control interventions in hotspots.
Study Information
- Study Type
- Cohort
- Research Domain
- Pathophysiology
- Evidence Level
- III - Observational genomic epidemiology across multiple cohorts and public genomes; no interventional components.
- Study Design
- OTHER