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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Score 2
2025 pubmed

An engineered antimicrobial peptide Z-FV7 demonstrates bactericidal efficacy against multidrug-resistant Escherichia coli in a murine model of endometritis.

Su. Jieru J; Yang. Hao H; Wang. Siyu S; Wang. Xue X; Li. Wei W; Meng. Wenwen W; Sun. Jiajun J; Zhu. Yaohong Y

Key Findings

  • Z‑FV7 showed a low minimum inhibitory concentration (32 µg/mL) against E. coli and other bacteria
  • In a mouse model of endometritis, Z‑FV7 reduced clinical symptoms and suppressed NF‑κB‑driven inflammatory cytokines (TNF‑α, IL‑1β, IL‑6)
  • Z‑FV7 increased tight‑junction proteins (Claudin‑1, ZO‑1), indicating improved tissue barrier function and displayed a favorable safety profile

Practical Outcomes

  • The work suggests engineered LL‑37‑based peptides could become powerful anti‑infection and anti‑inflammatory agents, but they are still far from human testing. For now, biohackers should view this as early‑stage research and wait for clinical data before considering any DIY applications.

Summary

Scientists created a new peptide called Z‑FV7 by adding part of the human antimicrobial peptide LL‑37 to a cow‑derived peptide. In mice with a uterine infection caused by drug‑resistant E. coli, Z‑FV7 lowered bacterial numbers, reduced inflammation, and helped keep the tissue barrier intact, performing similarly to antibiotics. The study is still in animals, so it isn’t ready for personal use yet.

Abstract

Endometritis is a common reproductive disorder in dairy cows, with antibiotics being the primary treatment option. However, the overuse of antibiotics has contributed to the growing problem of antimicrobial resistance. Antimicrobial peptides (AMPs) have been widely studied for their ability to kill bacteria and modulate immune responses. Previous research has focused on modifying natural AMPs extracted from Zophabas atratus haemolymph; however, these peptides have displayed limited effectiveness against bacteria. To overcome this limitation, researchers engineered a modified AMP, Z-FV7, by incorporating the sequence of the human-derived AMP LL-37. The resulting peptide demonstrated a favourable safety profile, with a minimum inhibitory concentration (MIC) reduced to 32 μg/mL and improved antibacterial activity against pathogens such as Staphylococcus aureus and Pseudomonas aeruginosa. Z-FV7 was tested in a bovine uterine epithelial cell model infected with Escherichia coli and in a murine model of endometritis. The findings showed that Z-FV7 alleviated clinical symptoms, inhibited the activation of the NF-κB signalling pathway induced by drug-resistant E. coli, reduced the expression of pro-inflammatory cytokines (TNF-α, IL-1β, IL-6), and promoted the expression of tight junction proteins (Claudin-1 and ZO-1). These results indicated that Z-FV7 can help reduce uterine inflammation and provide therapeutic outcomes similar to those of antibiotics during E. coli infection. Overall, Z-FV7 holds promise as a potential alternative to antibiotics for treating endometriosis in the future.

Study Information

Provider

pubmed

Year

2025

Date

2025-07-25T00:00:00.000Z

DOI

10.1186/s13567-025-01593-x

References

36