# Klebsiella pneumoniae and pyogenic liver abscess: Emerging clinical threats, virulence mechanisms and therapeutic strategies (Review)

**Authors:** Gulam Mustafa Hasan, Taj Mohammad, Sobia Zaidi, Anas Shamsi, Sukhwinder Singh Sohal, Md. Imtaiyaz Hassan

PMC · DOI: 10.3892/mmr.2026.13800 · Molecular Medicine Reports · 2026-01-13

## TL;DR

This review discusses the growing threat of Klebsiella pneumoniae causing liver abscesses, focusing on virulence, drug resistance, and new treatment strategies.

## Contribution

The paper provides a comprehensive review of emerging threats, virulence mechanisms, and therapeutic strategies for K. pneumoniae-associated pyogenic liver abscess.

## Key findings

- Hypervirulent and multidrug-resistant K. pneumoniae strains are increasingly causing severe liver abscesses.
- Rapid diagnostic tools like metagenomic sequencing and MALDI-TOF offer improved detection and treatment optimization.
- Current antibiotics face limitations, prompting exploration of anti-virulence and immunomodulatory approaches.

## Abstract

Klebsiella pneumoniae has emerged as a leading cause of pyogenic liver abscess (PLA), driven by hypervirulent and multidrug-resistant (MDR) strains that pose major diagnostic and therapeutic challenges. This organism exhibits extensive capsular diversity (K1-K80), with serotypes K1, K2, K5, K20, K54 and K57 being the most associated with invasive infections and severe clinical outcomes. Increasing convergence between hypervirulence and MDR determinants threatens effective management worldwide. Pharmacological and safety limitations of current antibiotics, including nephrotoxicity of colistin, hepatotoxicity of tigecycline and poor drug penetration into abscess cavities, further complicate treatment and encourage exploration of non-traditional strategies such as anti-virulence or immunomodulatory approaches. Recent advancements in rapid diagnostic tools such as metagenomic sequencing, MALDI-TOF and point-of-care PCR assays offer promising prospects for early detection and antimicrobial optimization. Pharmacokinetic challenges at the abscess site and the emergence of hybrid hvKp-MDR strains emphasize the urgency of precision-guided therapy and robust global surveillance. K. pneumoniae-associated PLA thus represents an evolving global health threat and understanding serotype diversity, antibiotic limitations and diagnostic innovations is essential for developing more effective preventive and therapeutic strategies. The present review provides current insights into the epidemiology, pathogenesis and therapeutic challenges of K. pneumoniae-associated PLA, while highlighting translational opportunities and research priorities to counter the escalating dual threat of hypervirulence and resistance.

## Linked entities

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

## Full-text entities

- **Genes:** Carbapenemase [NCBI Gene 13913776], New Delhi metallo-beta-lactamase [NCBI Gene 18983573], OXA-48 [NCBI Gene 15842812], CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, extended-spectrum beta-lactamase [NCBI Gene 13982007], beta-lactamase [NCBI Gene 18262323], metallo-beta-lactamase [NCBI Gene 11934636]
- **Diseases:** diabetes (MESH:D003920), pulmonary emboli (MESH:D020766), necrotizing fasciitis (MESH:D019115), metastasis (MESH:D009362), endogenous (MESH:D003866), Chronic liver disease (MESH:D008107), enteric abscesses (MESH:D004751), bacteremia (MESH:D016470), hepatocellular injury (MESH:D056486), Hypermucoviscous capsule (MESH:D002062), nosocomial infections (MESH:D003428), biliary tract disease (MESH:D001660), abdominal pain (MESH:D015746), dysbiosis (MESH:D064806), necrosis (MESH:D009336), rupture (MESH:D012421), MDR (MESH:D018088), fever (MESH:D005334), K. pneumoniae liver abscess (MESH:D008100), NDM (MESH:D007562), Klebsiella pneumoniae (MESH:D007710), brain abscess (MESH:D001922), abscess (MESH:D000038), colorectal carcinogenesis (MESH:D063646), CRKP (MESH:D011014), meningitis (MESH:D008580), inflammation (MESH:D007249), septic shock (MESH:D012772), Endophthalmitis (MESH:D009877), vision loss (MESH:D014786), appendicitis (MESH:D001064), biliary obstruction (MESH:D001658), Metastatic infections (MESH:D007239), portal hypertension (MESH:D006975), nephro- and ototoxicity (MESH:D006311), hyperglycemia (MESH:D006943), hepatobiliary abnormality (MESH:D004066), K. pneumoniae PLA (MESH:D046290), hypoxic (MESH:D002534), intra-abdominal (MESH:D000082122), invasive (MESH:D009361), malignancies (MESH:D009369), cirrhosis (MESH:D005355), intra-abdominal infections (MESH:D059413), bloodstream infections (MESH:D018805), peritonitis (MESH:D010538), organ failure (MESH:D009102), urinary tract infections (MESH:D014552), toxicity (MESH:D064420), ventilator-associated pneumonia (MESH:D053717)
- **Chemicals:** Cefiderocol (MESH:C000612166), yersiniabactin (MESH:C104398), relebactam (MESH:C568736), Tigecycline (MESH:D000078304), meropenem (MESH:D000077731), plazomicin (MESH:C550938), LPS (MESH:D008070), polysaccharide (MESH:D011134), ceftazidime (MESH:D002442), beta-lactam (MESH:D047090), imipenem (MESH:D015378), fluoroquinolone (MESH:D024841), O-antigen (MESH:D019081), lipid (MESH:D008055), ceftriaxone (MESH:D002443), ceftazidime-avibactam (MESH:C000595613), enterobactin (MESH:D004758), eravacycline (MESH:C571179), aerobactin (MESH:C031819), Carbapenem (MESH:D015780), salmochelin (MESH:C000630262), Aminoglycoside (MESH:D000617), CTX-M (-), cephalosporin (MESH:D002511), CR (MESH:D002857), iron (MESH:D007501), tetracycline (MESH:D013752)
- **Species:** Bacteriophage sp. (species) [taxon 38018], Homo sapiens (human, species) [taxon 9606], Klebsiella pneumoniae (species) [taxon 573]

## Full text

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## Figures

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## References

127 references — full list in the complete paper: https://tomesphere.com/paper/PMC12829308/full.md

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Source: https://tomesphere.com/paper/PMC12829308