Carbapenem-resistant hypervirulent Klebsiella pneumoniae: molecular evolution, diagnostic markers, and therapeutic
Tokeshwar Kumar Sahu1, Pravin Gadkari2, Jaishriram Rathored3,4
1Department of Microbiology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, India.
Abstract:
Carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKp) is an emerging convergent pathotype in which antimicrobial resistance (AMR) and invasive virulence increasingly overlap. This Mini Review critically summarizes how CR-hvKp arises through acquisition of carbapenemase-encoding plasmids by hypervirulent backgrounds, acquisition of virulence plasmids by established carbapenem-resistant lineages, and formation of hybrid resistance-virulence elements. It also discusses why laboratory recognition remains challenging, since carbapenem resistance, hypermucoviscosity, capsule type, and individual virulence markers are each informative but insufficient alone. A tiered diagnostic approach that integrates susceptibility testing, carbapenemase classification, virulence-marker profiling, capsule and sequence typing, and genome sequencing is therefore more appropriate for high-risk isolates. Therapeutic management remains difficult because available agents must be selected according to carbapenemase class, infection site, source control, susceptibility profile, and risk of resistance emergence. Available evidence supports prioritizing earlier recognition, plasmid-aware surveillance, antimicrobial stewardship, and outcome-focused studies as priorities for improving management of this high-risk convergent pathotype.
Insights
Carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKp) emerges from combined resistance and virulence traits. Early recognition and integrated diagnostics are crucial for managing this challenging pathogen.
Area of Science:
- Microbiology
- Infectious Diseases
- Genetics
Background:
- Carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKp) represents a significant public health threat, merging antimicrobial resistance (AMR) with high invasive potential.
- This emergent pathotype arises from the interplay of resistance and virulence factors, often mediated by plasmids.
Purpose of the Study:
- To critically review the emergence mechanisms of CR-hvKp.
- To discuss the challenges in laboratory recognition and propose diagnostic strategies.
- To outline therapeutic considerations and future research priorities for CR-hvKp.
Main Methods:
- Literature review and synthesis of current knowledge on CR-hvKp.
- Analysis of genetic mechanisms underlying resistance and virulence.
- Evaluation of diagnostic and therapeutic approaches.
Main Results:
- CR-hvKp develops through plasmid acquisition by either hypervirulent or carbapenem-resistant strains, or via hybrid elements.
- Laboratory identification is complex, requiring a combination of tests rather than single markers.
- Effective treatment necessitates careful consideration of carbapenemase type, infection site, and patient factors.
Conclusions:
- A tiered diagnostic approach integrating various methods is essential for accurate CR-hvKp identification.
- Management requires a multifaceted strategy including antimicrobial stewardship, surveillance, and outcome-focused research.
- Prioritizing early recognition and plasmid-aware surveillance is key to combating CR-hvKp.
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