# Dual action of herbal compounds in Klebsiella pneumoniae infection and associated inflammatory diseases

**Authors:** Uzma Saqib, Sakina Ratlamwala, Nidhi Kibe, Mirza S. Baig, Krishnan Hajela, Sadhana Sharma

PMC · DOI: 10.3389/fimmu.2026.1767981 · Frontiers in Immunology · 2026-02-23

## TL;DR

This review explores how herbal compounds can fight Klebsiella pneumoniae infections and reduce inflammation, offering a dual-action approach for better treatment outcomes.

## Contribution

The paper uniquely focuses on the dual antibacterial and immunomodulatory effects of phytochemicals against Klebsiella pneumoniae.

## Key findings

- Phytochemicals like curcumin and berberine show potential to reduce both infection and inflammation in Kp.
- Combining phytochemicals with antibiotics enhances bacterial clearance and reduces antibiotic use.
- The review highlights translational challenges and provides a framework for future phytochemical development.

## Abstract

Klebsiella pneumoniae (Kp) is a multidrug-resistant (MDR) pathogen responsible for severe infections such as pneumonia, sepsis, and urinary tract infections. Its pathogenicity includes both bacterial virulence factors and host-driven inflammatory responses thereby complicating treatment outcomes. Herbal compounds (phytochemicals) have recently gained attention as promising dual-action therapeutic agents that target both infection and inflammation. Phytochemicals such as curcumin, berberine, quercetin, resveratrol, and several medicinal plant extracts have demonstrated an integrated ability to mitigate both infection as well as host inflammation in preclinical studies. Their ability to attenuate virulence, reduce oxidative stress, and regulate host immune signaling positions them as potential candidates for adjunctive therapy against Kp infections. Furthermore, phytochemical-antibiotic combinations demonstrate synergistic effects, enhancing bacterial clearance and reducing antibiotic dosage requirements. Overall, the dual action of phytochemicals makes them as valuable candidates for integrative therapies against Kp infections and related inflammatory diseases. Unlike the prior reviews, the present review uniquely focusses the dual antibacterial and immunomodulatory actions of plant-derived compounds against Kp. It adds a novel perspective integrating the therapeutic promise of phytochemicals with a systematic analysis of their translational limitations. Further, it provides a rational framework to guide future development of phytochemicals as potent and clinically viable therapeutics against Kp infections.

## Linked entities

- **Chemicals:** curcumin (PubChem CID 969516), berberine (PubChem CID 2353), quercetin (PubChem CID 5280343), resveratrol (PubChem CID 5056)
- **Diseases:** pneumonia (MONDO:0005249)
- **Species:** Klebsiella pneumoniae (taxon 573)

## Full-text entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615] {aka IMD68, MYD88D, WM1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** organ dysfunction (MESH:D009102), lung inflammation (MESH:D011014), acute respiratory distress syndrome (MESH:D012128), fibrosis (MESH:D005355), inflammation (MESH:D007249), MDR (MESH:D018088), Klebsiella pneumoniae infection (MESH:D007710), septic shock (MESH:D012772), bloodstream infection (MESH:D018805), infectious (MESH:D003141), tissue damage (MESH:D017695), Infection (MESH:D007239), urinary tract infections (MESH:D014552), cytotoxicity (MESH:D064420)
- **Chemicals:** kaempferol (MESH:C006552), meropenem (MESH:D000077731), carbapenems (MESH:D015780), Alkaloids (MESH:D000470), thymol (MESH:D013943), resveratrol (MESH:D000077185), 1,8-cineol (MESH:D000077591), Allyl isothiocyanate (MESH:C004471), aminoglycoside (MESH:D000617), quercetin (MESH:D011794), cefiderocol (MESH:C000612166), rutin (MESH:D012431), LPS (MESH:D008070), beta-lactam (MESH:D047090), ROS (MESH:D017382), BBR (MESH:D001599), baicalein (MESH:C006680), Flavonoids (MESH:D005419), vaborbactam (MESH:C000626994), curcumin (MESH:D003474), carvacrol (MESH:C073316), Herbal compounds (-), NAR (MESH:C005274), ceftazidime-avibactam (MESH:C000595613), propolis (MESH:D011429), monoterpenes (MESH:D039821)
- **Species:** Acorus calamus (Eurasian sweet-flag, species) [taxon 4465], Rhazya stricta (species) [taxon 396313], Klebsiella pneumoniae (species) [taxon 573], Andrographis paniculata (species) [taxon 175694], Citrus maxima (buntan, species) [taxon 37334], Bacteriophage sp. (species) [taxon 38018], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12968187/full.md

## References

154 references — full list in the complete paper: https://tomesphere.com/paper/PMC12968187/full.md

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Source: https://tomesphere.com/paper/PMC12968187