# Antibacterial efficacy and mechanism of the novel antimicrobial peptide lachnospirin-1 against Acinetobacter baumannii

**Authors:** Pengfei She, Mengna Li, Yiqing Liu, Guanqing Huang, Shaowei Guo, Dan Xiao, Yelan Hong, Lihua Lu, Yong Wu

PMC · DOI: 10.1080/21505594.2026.2646808 · Virulence · 2026-03-16

## TL;DR

A new antimicrobial peptide called lachnospirin-1 shows strong effectiveness against drug-resistant Acinetobacter baumannii infections.

## Contribution

Lachnospirin-1 is a novel antimicrobial peptide with potent activity against CRAB and multiple mechanisms of action.

## Key findings

- Lachnospirin-1 effectively kills CRAB and eliminates biofilms and persister cells.
- The peptide disrupts bacterial membranes, neutralizes lipopolysaccharide, and induces oxidative stress.
- Mouse models confirmed its safety and in vivo bactericidal activity.

## Abstract

The treatment of carbapenem-resistant A. baumannii (CRAB) infections has become a major global medical challenge; therefore, there is an urgent need for new antimicrobial development. Antimicrobial peptides hold great promising potential due to their rapid bactericidal activity and low induction of drug resistance. In this study, we screened and synthesized the antimicrobial peptide lachnospirin-1, which exhibited significant bactericidal activity against CRAB and can also effectively eliminate its biofilms and persister cells. Mechanism studies, including fluorescent probe detection, transmission electron microscopy observations, and molecular dynamics simulations, et al. indicated that lachnospirin-1 exerts its effects through multiple mechanisms, such as disrupting bacterial cell membranes, neutralizing lipopolysaccharide, as well as inducing oxidative stress, which also demonstrates its certain potential. In addition, the favorable safety profile and effective in vivo bactericidal activity of lachnospirin-1 were determined by mouse models. Overall, our study found that lachnospirin-1 has considerable research potential as a lead compound and possesses latent value as a clinical therapy for refractory infections caused by CRAB.

## Linked entities

- **Species:** Acinetobacter baumannii (taxon 470)

## Full-text entities

- **Genes:** APRT (adenine phosphoribosyltransferase) [NCBI Gene 353] {aka AMP, APRTD}, CTRL (chymotrypsin like) [NCBI Gene 1506] {aka CTRL1}
- **Diseases:** toxicity (MESH:D064420), wound infection (MESH:D014946), CRAB (MESH:D060467), A. baumannii infections (MESH:D007239), respiratory tract infections (MESH:D012141), abscess (MESH:D000038), bacterial (MESH:D001424), nosocomial infections (MESH:D003428), Inflammatory (MESH:D007249), MDR-AB (MESH:D018088), cutaneous (MESH:D018366), hyperammonemia (MESH:D022124), urinary tract infections (MESH:D014552), Hemolysis (MESH:D006461), meningitis (MESH:D008580), sepsis (MESH:D018805)
- **Chemicals:** FITC (MESH:D016650), POPG (MESH:C060037), CL (MESH:D002713), ammonium (MESH:D064751), PI (MESH:D011419), paraformaldehyde (MESH:C003043), alcohol (MESH:D000438), eosin (MESH:D004801), magnesium chloride (MESH:D015636), carbapenem (MESH:D015780), 1,2-dioleoyl-sn-glycero-3-phosphocholine (MESH:C017251), resin (MESH:D012116), lipid (MESH:D008055), uranyl acetate (MESH:C005460), xylene (MESH:D014992), HEPES (MESH:D006531), glycerol (MESH:D005990), calcium chloride (MESH:D002122), ADP (MESH:D000244), ammonium sulfate (MESH:D000645), 1-palmitoyl-2-oleoyl-sn-glycero-3- phosphocholine (MESH:C028694), benzoquinone (MESH:C004532), 1-N-phenylnaphthylamine (MESH:C005444), Cholesterol (MESH:D002784), BHI (-), 1,2-dioleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) (MESH:C051388), SM (MESH:D012493), Cr (MESH:D002857), streptomycin (MESH:D013307), zinc chloride (MESH:C016837), H (MESH:D006859), potassium chloride (MESH:D011189), superoxide (MESH:D013481), Triton X-100 (MESH:D017830), ethanol (MESH:D000431), CV (MESH:D005840), oxygen (MESH:D010100), CR-AB (MESH:C059745), C (MESH:D002244), polystyrene (MESH:D011137), hematoxylin (MESH:D006416), LPS (MESH:D008070), ATP (MESH:D000255), Tobramycin (MESH:D014031), DiSC3 (5) (MESH:C012944), glutaraldehyde (MESH:D005976), copper (MESH:D003300), saline (MESH:D012965), iron chloride (MESH:C024555), AMPs (MESH:D000089882), ammonium chloride (MESH:D000643), DCF (MESH:D015649), water (MESH:D014867), FM4-64 (MESH:C092350), osmium tetroxide (MESH:D009993), SYTO9 (MESH:C103389), isoflurane (MESH:D007530), DCFDA (MESH:C029569), ROS (MESH:D017382), epoxy resin (MESH:D004853)
- **Species:** Homo sapiens (human, species) [taxon 9606], Enterococcus faecium (species) [taxon 1352], Pseudomonas aeruginosa PAO1 (strain) [taxon 208964], Mus musculus (house mouse, species) [taxon 10090], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Klebsiella pneumoniae (species) [taxon 573], Escherichia coli (E. coli, species) [taxon 562], Enterococcus faecalis (species) [taxon 1351], Acinetobacter baumannii (species) [taxon 470], Pseudomonas aeruginosa (species) [taxon 287], Escherichia coli ATCC 25922 (strain) [taxon 1322345]
- **Cell lines:** AB1069 — Homo sapiens (Human), Transformed cell line (CVCL_9D73), O55:B5 — Mus musculus (Mouse), Hybridoma (CVCL_C4LC)

## Full text

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## Figures

14 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13007424/full.md

## References

71 references — full list in the complete paper: https://tomesphere.com/paper/PMC13007424/full.md

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Source: https://tomesphere.com/paper/PMC13007424