Published by Elsevier Inc.
Temporin A is effective in MRSA-infected wounds through bactericidal activity and acceleration of wound repair in a murine model
Received 17 October 2007;
Abstract
We investigated the effect of topical temporin A in the management of methicillin-resistant strain of Staphylococcus aureus (MRSA)-infected experimental surgical wounds in mice. The wound, cut through the panniculus carnosus of BALB/c mice, was inoculated with 5 × 107 colony-forming units of MRSA. Mice were treated with Allevyn, temporin A-soaked Allevyn, Allevyn and daily intraperitoneal teicoplanin (7 mg/kg), temporin A-soaked Allevyn and daily intraperitoneal teicoplanin. Main outcome measurements were: quantitative bacterial culture, histological examination with assessment of micro-vessel density and of vascular endothelial growth factor (VEGF) expression in tissue sections, and VEGF plasma levels alike. Treatment with temporin-A associated with teicoplanin injection significantly reduced bacterial load to 0.85 × 101 ± 0.1 × 101 CFU/ml. Histological examination showed that infected mice receiving temporin A-soaked Allevyn (with or without teicoplanin) had a higher degree of granulation tissue formation and collagen deposition compared to the other treated groups. A significant increase in serum VEGF expression was observed in mice receiving temporin A topically and temporin A topically associated with intraperitoneal teicoplanin. In conclusion our results demonstrated that temporin A is effective in the management of infected wounds, by a significant bacterial growth inhibition and acceleration of wound repair process.
Keywords: Temporin A; MRSA infection; Wound repair; Teicoplanin; VEGF
Article Outline
- 1. Introduction
- 2. Materials and methods
- 2.1. Organisms
- 2.2. Animals
- 2.3. Drugs
- 2.4. Preparation of inoculum
- 2.5. Mice model
- 2.6. Histological examination of excised tissues
- 2.7. Angiogenesis in the infected wound
- 2.8. Vascular endothelial growth factor plasma levels
- 2.9. Statistical analysis
- 3. Results
- 3.1. Quantitative culture of excised tissues
- 3.2. Histological examination of excised tissues and assessment of angiogenesis (Table 2 and Table 3)
- 3.3. VEGF plasma levels
- 4. Discussion
- 5. Conclusion
- Conflicts of interest
- Acknowledgements
- References






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