# Co-evolution of resistance and virulence in Klebsiella pneumoniae liver abscess: PLA-specific mechanisms and therapeutic dilemmas

**Authors:** Han Lin, Zhenghaoyu Huang, Yonghong Guo

PMC · DOI: 10.3389/fcimb.2026.1767477 · Frontiers in Cellular and Infection Microbiology · 2026-02-10

## TL;DR

This review explores how Klebsiella pneumoniae combines drug resistance and high virulence in liver abscesses, complicating diagnosis and treatment.

## Contribution

The paper consolidates current knowledge on PLA-specific mechanisms of CR-hvKP and proposes translational strategies for managing these infections.

## Key findings

- CR-hvKP combines carbapenem resistance with hypervirulence through plasmid fusion and horizontal gene transfer.
- Key virulence factors like K1/K2 capsule and aerobactin are critical for hepatic infection in PLA.
- Rapid diagnostics and anti-virulence strategies are emerging as potential solutions for CR-hvKP management.

## Abstract

The co-evolution of resistance and virulence in Klebsiella pneumoniae poses a significant challenge in the management of pyogenic liver abscesses (PLA), particularly with the advent of carbapenem-resistant hypervirulent K. pneumoniae (CR-hvKP). This review specifically addresses PLA to consolidate current knowledge on how key virulence factors—such as the K1/K2 capsule, hypermucoviscosity, and aerobactin—contribute to hepatic infection. It also examines the molecular mechanisms, including plasmid fusion and horizontal gene transfer, that are believed to facilitate the convergence of hypervirulence and carbapenem resistance. Additionally, the review discusses the unique clinical challenges presented by CR-hvKP in the context of PLA, including diagnostic delays, antimicrobial treatment failures, and complications in drainage. Emerging countermeasures, such as rapid molecular diagnostics and novel anti-virulence strategies, are also explored. By integrating contemporary molecular insights with the specific clinical challenges of PLA management, this review provides an updated translational perspective aimed at bridging the gap between pathogenesis and therapeutic strategies for CR-hvKP-associated infections.

## Linked entities

- **Species:** Klebsiella pneumoniae (taxon 573)

## Full-text entities

- **Genes:** LONP1 (lon peptidase 1, mitochondrial) [NCBI Gene 9361] {aka CODASS, LON, LONP, LonHS, PIM1, PRSS15}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, extended-spectrum beta-lactamase [NCBI Gene 13982007], LCN2 (lipocalin 2) [NCBI Gene 3934] {aka 24p3, MSFI, NGAL, p25}, C3 (complement C3) [NCBI Gene 718] {aka AHUS5, ARMD9, ASP, C3a, C3b, CPAMD1}, RmpA [NCBI Gene 2657583], CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** hypoxia (MESH:D000860), neutrophil dysfunction (MESH:C564942), hematologic malignancies (MESH:D019337), purulent meningitis (MESH:D008586), micro-abscesses (MESH:C536681), CRKP (MESH:D011014), hypoxic (MESH:D002534), metastatic (MESH:D000092182), gut dysbiosis (MESH:D064806), Hypervirulent Klebsiella pneumoniae (MESH:D007710), diabetes (MESH:D003920), antibiotic (MESH:D004761), Hyperglycemia (MESH:D006943), critical illness (MESH:D016638), abscess (MESH:D000038), inflammation (MESH:D007249), bacteremic liver abscess (MESH:D008100), pulmonary infections (MESH:D012141), HL (MESH:C538324), invasive (MESH:D009361), bloodstream infections (MESH:D018805), necrosis (MESH:D009336), CPS (MESH:C564877), septic shock (MESH:D012772), central nervous system infections (MESH:D002494), hepatic infection (MESH:D056486), organ damage (MESH:D000092124), type 2 diabetes (MESH:D003924), PLA (MESH:D046290), endophthalmitis (MESH:D009877), Infections (MESH:D007239), Impairment of neutrophil (MESH:C564275), death (MESH:D003643), Hyperglycemic (MESH:D006944), nosocomial infections (MESH:D003428)
- **Chemicals:** cAMP (MESH:D000242), blood glucose (MESH:D001786), gentamicin (MESH:D005839), iron (MESH:D007501), Carbapenem (MESH:D015780), tigecycline (MESH:D000078304), boric acid (MESH:C032688), polysaccharide (MESH:D011134), aminoglycosides (MESH:D000617), mannose (MESH:D008358), meropenem/vaborbactam (MESH:C000654127), eugenol (MESH:D005054), glucose (MESH:D005947), fumarate (MESH:D005650), beta-lactam (MESH:D047090), citrate (MESH:D019343), fluoroquinolones (MESH:D024841), CR (MESH:D002857), cephalosporins (MESH:D002511), salmochelin (MESH:C000630262), CAZ-AVI (MESH:C000595613), Aerobactin (MESH:C031819), bile salts (MESH:D001647), CPS (-)
- **Species:** Klebsiella pneumoniae (species) [taxon 573], Mus musculus (house mouse, species) [taxon 10090], Bacteriophage sp. (species) [taxon 38018], Homo sapiens (human, species) [taxon 9606], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395]
- **Cell lines:** ST11 — Homo sapiens (Human), Lung non-small cell carcinoma, Cancer cell line (CVCL_7025)

## Full text

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## Figures

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## References

113 references — full list in the complete paper: https://tomesphere.com/paper/PMC12929503/full.md

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Source: https://tomesphere.com/paper/PMC12929503