Evaluation of the Antimicrobial Peptide, RP557, for the Broad-Spectrum Treatment of Wound Pathogens and Biofilm.
Woodburn. Kathryn Wynne KW; Jaynes. Jesse M JM; Clemens. L Edward LE
Key Findings
- RP557 shows broad‑spectrum killing of Gram‑positive, Gram‑negative bacteria and fungi, including tough biofilms.
- Repeated low‑dose exposure did not lead to resistance in Pseudomonas aeruginosa or Staphylococcus aureus, unlike gentamicin and clindamycin.
- A 0.2% topical formulation cleared MRSA infections completely in a mouse wound model.
Practical Outcomes
- For now, the main takeaway is that RP557 could become a powerful, resistance‑proof topical antiseptic for wounds, especially in settings where infections are hard to treat. Biohackers should watch for future clinical trials, but there’s no immediate protocol to adopt until the peptide is approved for human use.
Summary
Researchers created a new antimicrobial peptide called RP557, modeled after the natural human peptide LL-37. In lab tests and mouse wound models, RP557 killed a wide range of bacteria and fungi, stopped biofilm formation, and didn’t cause resistance like some antibiotics do. While the results are promising, the peptide isn’t yet available for human use, so it’s more of a future option than something you can try now.
Abstract
The relentless growth of multidrug resistance and generation of recalcitrant biofilm are major obstacles in treating wounds, particularly in austere military environments where broad-spectrum pathogen coverage is needed. Designed antimicrobial peptides (dAMPs) are constructed analogs of naturally occurring AMPs that provide the first line of defense in many organisms. RP557 is a dAMP resulting from iterative rational chemical structural analoging with endogenous AMPs, human cathelicidin LL-37 and Tachyplesin 1 and the synthetic D2A21 used as structural benchmarks. RP557 possesses broad spectrum activity against Gram-positive and Gram-negative bacteria and fungi, including recalcitrant biofilm with substantial selective killing over bacterial cells compared to mammalian cells. RP557 did not induce resistance following chronic passages of <i>Pseudomonas aeruginosa</i> and <i>Staphylococcus aureus</i> at subinhibitory concentrations, whereas concurrently run conventional antibiotics, gentamycin, and clindamycin, did. Furthermore, RP557 was able to subsequently eliminate the generated gentamycin resistant <i>P. aeruginosa</i> and clindamycin resistant <i>S. aureus</i> strains without requiring an increase in minimum inhibitory concentration (MIC) concentrations. RP557 was evaluated further in a MRSA murine wound abrasion infection model with a topical application of 0.2% RP557, completely eliminating infection. If these preclinical results are translated into the clinical setting, RP557 may become crucial for the empirical broad-spectrum treatment of wound pathogens, so that infections can be reduced to a preventable complication of combat-related injuries.
Study Information
pubmed
2019
2019-07-24T00:00:00.000Z
10.3389/fmicb.2019.01688
45
38