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LL-37

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

Quick Stats
Studies 2230
Trials 95
Score 3
2019 pubmed 32 citations

Design and antimicrobial activities of LL-37 derivatives inhibiting the formation of Streptococcus mutans biofilm.

Chen. Zhao Z; Yang. Guang G; Lu. Shengsheng S; Chen. Daiwei D; Fan. Sheng S; Xu. Junyang J; Wu. Buling B; He. Jian J

Key Findings

  • IG‑13‑1 and IG‑13‑2 stop S. mutans growth at about 5 µM (MIC)
  • They prevent biofilm formation at ~6‑8 µM (MBIC)
  • They kill bacteria by disrupting membranes and lower inflammatory markers (TNF‑α, NF‑κB)

Practical Outcomes

  • These peptides could be the basis for future anti‑cavity mouthwashes or toothpaste, but they aren’t commercially available yet. For now, the takeaway is that targeting bacterial membranes and inflammation is a viable strategy for oral health, and any DIY attempts should wait for safe, tested formulations.

Summary

Researchers tweaked the human peptide LL‑37 and created two shorter versions, IG‑13‑1 and IG‑13‑2, that can kill the cavity‑causing bacteria Streptococcus mutans and stop it from forming sticky biofilm on teeth. They work by punching holes in the bacterial membrane and also calm down inflammation signals. The work is still in the lab, but it shows a promising route for new mouth‑care products.

Abstract

Dental plaque is closely related to the occurrence of dental caries, of which the main causative bacterium is Streptococcus mutans (S. mutans). In this study, to create potent antibiofilm agents, we chose a human antimicrobial peptide LL-37 as our starting material and modified it by cutting it shorter and varying its charge and hydrophobicity. The results of anti-S. mutans as well as biofilm inhibitory activity tests indicated that two derivatives, IG-13-1 and IG-13-2, were the most potent one toward both planktonic and biofilm S. mutans cells with the minimal inhibitory concentration of 5.0 μM and minimal biofilm inhibitory concentrations of 5.91 ± 0.91 μM and 7.58 ± 0.23 μM, respectively. The modes of action study showed that IG-13-1 and IG-13-2 were functioned by disrupting the bacterial membrane, causing the leakage of inner contents, thereby leading to the death of bacterial cells eventually. In addition, IG-13-1 and IG-13-2 were able to suppress the expression of proinflammatory cytokine of TNF-α and reduce the level of nuclear transcription factor-κB, which indicated the potential anti-inflammatory activity of these peptides. Conclusively, this study indicated that IG-13-1 and IG-13-2 are potent peptides in both anti-S. mutans and anti-inflammatory activities, therefore, showing a potential application for the prevention and treatment of dental caries.

Study Information

Provider

pubmed

Year

2019

Date

2019-01-11T00:00:00.000Z

DOI

10.1111/cbdd.13419

Citations

32

References

37