Tissue nano-transfection of antimicrobial genes drives bacterial biofilm killing in wounds and is potentially mediated by extracellular vesicles.
Cuellar-Gaviria. Tatiana Z TZ; Rincon-Benavides. Maria Angelica MA; Halipci Topsakal. Hatice Nur HN; Salazar-Puerta. Ana Isabel AI; Jaramillo-Garrido. Shara S; Kordowski. Mia M; Vasquez-Martinez. Carlos A CA; Nguyen. Kim Truc KT; Rima. Xilal Y XY; Rana. Pranav S J B PSJB; Combita-Heredia. Orlando O; Deng. Binbin B; Dathathreya. Kavya K; McComb. David W DW; Reategui. Eduardo E; Wozniak. Daniel D; Higuita-Castro. Natalia N; Gallego-Perez. Daniel D
Key Findings
- Tissue nano‑transfection (TNT) successfully delivered the CAMP gene to mouse skin cells, raising LL‑37 production.
- Extracellular vesicles from transfected cells carried extra LL‑37 and its mRNA, potentially spreading the antimicrobial effect.
- In infected mouse wounds, daily TNT treatment for 4 days dramatically lowered bacterial load, reduced biofilm, and increased healing markers like macrophage recruitment and vascularization.
Practical Outcomes
- The study shows that boosting LL‑37 locally can fight wound infections and improve healing, but the method relies on a specialized gene‑delivery device tested only in mice. For biohackers, it suggests that topical approaches that raise LL‑37 (e.g., creams with LL‑37 peptide or agents that stimulate its production) might be worth exploring, though safe human protocols are not yet established.
Summary
Scientists used a tiny‑needle‑like technique to deliver a gene that makes the natural antimicrobial peptide LL‑37 directly into mouse skin wounds. This boosted LL‑37 levels, cut down Staph bacteria and biofilm, and helped the wounds heal faster with more immune cells and blood vessels.
Abstract
The emergence of bacteria that are resistant to antibiotics is on track to become a major global health crisis. Therefore, there is an urgent need for new treatment options. Here, we studied the implementation of tissue-nanotransfection (TNT) to treat Staphylococcus aureus-infected wounds by delivering gene cargos that boost the levels of naturally produced antimicrobial peptides. The Cathelicidin Antimicrobial Peptide gene (CAMP), which produces the antimicrobial peptide LL-37, was used as model gene cargo. In vitro evaluation showed successful transfection and an increase in the transcription and translation of CAMP-coding plasmid in mouse primary epithelial cells. Moreover, we found that the extracellular vesicles (EVs) derived from the transfected cells (in vitro and in vivo) carried significantly higher concentrations of CAMP transcripts and LL-37 peptide compared to control EVs, possibly mediating the trafficking of the antimicrobial contents to other neighboring cells. The TNT platform was then used in vivo on an excisional wound model in mice to nanotransfect the CAMP-coding plasmid on the edge of infected wounds. After 4 days of daily treatment, we observed a significant decrease in the bacterial load in the CAMP-treated group compared to the sham group. Moreover, histological analysis and bacterial load quantification also revealed that TNT of CAMP on S. aureus-infected wounds was effective in treating biofilm progression by reducing the bacterial load. Lastly, we observed a significant increase in macrophage recruitment to the infected tissue, a robust increase in vascularization, as well as and an increased expression of IL10 and Fli1. Our results demonstrate that TNT-based delivery of gene cargos coding for antimicrobial compounds to the wound is a promising approach for combating biofilm infections in wounds.
Study Information
pubmed
2024
2024-11-13T00:00:00.000Z
10.1016/j.jconrel.2024.10.071
2
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