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Antimicrobial Peptides Produced by Selective Pressure Incorporation of Non-canonical Amino Acids
Published on: May 4, 2018
RNAIII-inhibiting-peptide-loaded polymethylmethacrylate prevents in vivo Staphylococcus aureus biofilm formation
Paloma Anguita-Alonso1, Andrea Giacometti, Oscar Cirioni
1Division of Infectious Diseases, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.
Abstract:
Staphylococci, common orthopedic pathogens, form antibiotic-resistant biofilms. Polymethylmethacrylate (PMMA) beads loaded with the quorum-sensing inhibitor RNAIII-inhibiting peptide (RIP) were implanted in rats and shown to prevent methicillin-resistant Staphylococcus aureus infection. RIP release was bimodal, typical of previously-tested antibiotics. These results suggest that RIP-PMMA warrants further evaluation for management of orthopedic infections caused by staphylococci.
Insights
RNAIII-inhibiting peptide (RIP) loaded polymethylmethacrylate (PMMA) beads prevented Staphylococcus aureus infections in rats. This study suggests RIP-PMMA beads are a promising strategy for managing staphylococcal orthopedic infections.
Area of Science:
- Orthopedic surgery
- Infectious disease
- Biomaterials science
Background:
- Staphylococci are common causes of orthopedic infections.
- These bacteria form antibiotic-resistant biofilms, complicating treatment.
- Current treatments face challenges due to rising antibiotic resistance.
Purpose of the Study:
- To evaluate the efficacy of polymethylmethacrylate (PMMA) beads loaded with RNAIII-inhibiting peptide (RIP) in preventing staphylococcal orthopedic infections.
- To assess the potential of RIP as a quorum-sensing inhibitor in a clinically relevant biomaterial.
Main Methods:
- Polymethylmethacrylate (PMMA) beads loaded with RNAIII-inhibiting peptide (RIP) were implanted in a rat model.
- The model was challenged with methicillin-resistant Staphylococcus aureus (MRSA) to assess infection prevention.
- RIP release kinetics from the PMMA beads were analyzed.
Main Results:
- PMMA beads loaded with RIP successfully prevented methicillin-resistant Staphylococcus aureus (MRSA) infection in the rat orthopedic model.
- The release profile of RIP from the PMMA beads was bimodal, similar to that of antibiotics.
- The findings demonstrate the potential of RIP-loaded PMMA for infection control.
Conclusions:
- RNAIII-inhibiting peptide (RIP)-loaded PMMA beads show significant promise for managing staphylococcal orthopedic infections.
- This approach offers a novel strategy to combat antibiotic-resistant bacterial biofilms.
- Further research into RIP-PMMA is warranted for clinical applications in orthopedic infection management.
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