# Ferroptosis-mediated intestinal decolonization of Klebsiella pneumoniae using Fe/PPy nanomaterials under near-infrared light

**Authors:** Xu Zhang, Zelin Yan, Binna Zhang, Siyu Shi, Yuchen Wu, Yanyan Zhang, Danxia Gu, Huqiang Tang, Rong Zhang

PMC · DOI: 10.3389/fmicb.2026.1749597 · Frontiers in Microbiology · 2026-02-20

## TL;DR

A new nanomaterial using iron and polypyrrole can kill drug-resistant Klebsiella bacteria through a process called ferroptosis when activated by near-infrared light.

## Contribution

Introduces a novel Fe/PPy nanocomposite that induces ferroptosis in Klebsiella pneumoniae under near-infrared light, offering a resistance-free antimicrobial strategy.

## Key findings

- Fe/PPy nanomaterials effectively induce bacterial lipid peroxidation via ferroptosis under near-infrared light.
- The nanomaterial achieves high in vivo antibacterial efficacy against Klebsiella pneumoniae without promoting resistance.
- Photothermal conversion and Fenton reaction synergistically enhance reactive oxygen species production for targeted bacterial killing.

## Abstract

Klebsiella pneumoniae (KP) is a Gram-negative bacterium with a thick capsule that confers natural drug resistance, making it a common opportunistic pathogen. In recent years, the spread of hypervirulent Klebsiella pneumoniae (hvKP) and carbapenem-resistant Klebsiella pneumoniae (CR-KP) strains has created major treatment challenges. Among these, of particular concern is carbapenem-resistant hypervirulent Klebsiella pneumoniae (CR-hvKP), which combines both hypervirulence and carbapenem resistance. This strain can persistently colonize the gut, facilitating resistance gene spread and causing bacterial translocation with subsequent infections. CR-hvKP has now become a key pathogen in both hospital and community settings. Traditional antibiotic treatments often lead to the emergence of bacterial resistance, necessitating the development of novel antimicrobial strategies.

This study introduces an iron-polypyrrole nanocomposite (Fe/PPy) designed to leverage an innovative mechanism of ferroptosis-induced bacterial killing. The nanomaterial possesses intrinsic Fenton reaction activity. Moreover, its photothermal conversion efficiency exceeds 85%. Under 1,064 nm near-infrared (NIR) light, its photothermal effect significantly enhances the Fenton reaction efficiency, thereby effectively catalyzing the conversion of bacterial endogenous H₂O₂ into reactive oxygen species (ROS), thereby inducing bacterial lipid peroxidation and achieving targeted bacterial killing via the ferroptosis pathway.

The excellent tissue penetration of 1,064 nm NIR light enables this material to act precisely on deep-seated infectious lesions, achieving in vivo antibacterial efficacy. Experimental results demonstrate that Fe/PPy nanomaterials exhibit high antimicrobial efficacy and safety against KP without readily inducing bacterial resistance.

This study provides a novel nanodrug design approach for the clinical treatment of KP infections, offering significant translational potential in the field of anti-infective therapy.

## Full-text entities

- **Genes:** Gpt (glutamic pyruvic transaminase, soluble) [NCBI Gene 76282] {aka 1300007J06Rik, 2310022B03Rik, ALT, ALT1, Gpt-1, Gpt1}, Slc17a5 (solute carrier family 17 (anion/sugar transporter), member 5) [NCBI Gene 235504] {aka 4631416G20Rik, 4732491M05, AST, ISSD, NSD, SD}, Alb (albumin) [NCBI Gene 11657] {aka Alb-1, Alb1, BCL001, BCL002, BPL001}
- **Diseases:** pneumonia (MESH:D011014), Hemolysis (MESH:D006461), inflammatory (MESH:D007249), cancer (MESH:D009369), KP (MESH:D007710), abnormalities in liver and kidney (MESH:D000015), edema (MESH:D004487), bacterial infections (MESH:D001424), dislocation (MESH:D004204), necrosis (MESH:D009336), intestinal infection (MESH:D007410), infectious (MESH:D003141), sepsis (MESH:D018805), infection (MESH:D007239), toxicity (MESH:D064420)
- **Chemicals:** Water (MESH:D014867), ertapenem (MESH:D000077727), MB (MESH:D008751), DCFH-DA (MESH:C029569), Fe (MESH:D007501), CAZ (MESH:D002442), Carbapenem (MESH:D015780), meropenem (MESH:D000077731), cefepime (MESH:D000077723), TBA (MESH:C029684), PVP (MESH:D011205), HCl (MESH:D006851), ethanol (MESH:D000431), hydroxyl radicals (MESH:D017665), gold (MESH:D006046), PI (MESH:D010716), FEP (MESH:D011138), oxygen (MESH:D010100), polypyrrole (MESH:C067635), tribromoethanol (MESH:C062527), EDTA (MESH:D004492), IMP (MESH:D007291), agar (MESH:D000362), FeCl3 (MESH:C024555), ciprofloxacin (MESH:D002939), DFO (MESH:D003676), tigecycline (MESH:D000078304), cefmetazole (MESH:D015311), imipenem (MESH:D015378), CO2 (MESH:D002245), Lipid (MESH:D008055), Urea Nitrogen (MESH:C530477), diethylene glycol (MESH:C013484), ETP (MESH:D005000), DMF (MESH:D004126), PB (MESH:D007854), glutaraldehyde (MESH:D005976), sodium acetate (MESH:D019346), eosin (MESH:D004801), beta-lactam (MESH:D047090), Heparin (MESH:D006493), membrane lipid (MESH:D008563), CRE (MESH:D003404), ROS (MESH:D017382), CAV (-), H2O2 (MESH:D006861), propidium iodide (MESH:D011419), H&amp;E (MESH:D006371), cefotaxime (MESH:D002439), Crystal violet (MESH:D005840), aztreonam (MESH:D001398), pyridine (MESH:C023666), sodium citrate (MESH:D000077559), ceftazidime/avibactam (MESH:C000595613), SYTO 9 (MESH:C103389), hematoxylin (MESH:D006416), ATM (MESH:C020809), piperacillin/tazobactam (MESH:D000077725), amikacin (MESH:D000583), MDA (MESH:D008315)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Klebsiella pneumoniae (species) [taxon 573], Klebsiella pneumoniae subsp. pneumoniae (subspecies) [taxon 72407], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** /6 — Homo sapiens (Human), Tongue squamous cell carcinoma, Cancer cell line (CVCL_5985), hvKP4 — Homo sapiens (Human), Ataxia telangiectasia syndrome, Finite cell line (CVCL_F083), 22ZR-42 — Cricetulus griseus (Chinese hamster), Transformed cell line (CVCL_8028), C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12963007/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12963007/full.md

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Source: https://tomesphere.com/paper/PMC12963007