Efficacy of Cathelicidin-Mimetic Antimicrobial Peptoids against Staphylococcus aureus
Aaron B Benjamin1, Madeleine G Moule1,2, Maruti K Didwania3
1Department of Microbial Pathogenesis and Immunology, Texas A&M Health Science Center, College Station, Texas, USA.
Abstract:
Staphylococcus aureus is one of the most common pathogens associated with infection in wounds. The current standard of care uses a combination of disinfection and drainage followed by conventional antibiotics such as methicillin. Methicillin and vancomycin resistance has rendered these treatments ineffective, often causing the reemergence of infection. This study examines the use of antimicrobial peptoids (sequence-specific poly-N-substituted glycines) designed to mimic naturally occurring cationic, amphipathic host defense peptides, as an alternative to conventional antibiotics. These peptoids also show efficient and fast (<30 min) killing of methicillin-susceptible S. aureus (MSSA) and methicillin-resistant S. aureus (MRSA) at low micromolar concentrations without having apparent cytotoxic side effects in vivo. Additionally, these novel peptoids show excellent efficacy against biofilm formation and detachment for both MSSA and MRSA. In comparison, conventional antibiotics were unable to detach or prevent formation of biofilms. One cationic 12mer, Peptoid 1, shows great promise, as it could prevent formation of and detach biofilms at concentrations as low as 1.6 μM. The use of a bioluminescent S. aureus murine incision wound model demonstrated clearance of infection in peptoid-treated mice within 8 days, conveying another advantage these peptoids have over conventional antibiotics. These results provide clear evidence of the potential for antimicrobial peptoids for the treatment of S. aureus wound infections. IMPORTANCE Staphylococcus aureus resistance is a consistent problem with a large impact on the health care system. Infections with resistant S. aureus can cause serious adverse effects and can result in death. These antimicrobial peptoids show efficient killing of bacteria both as a biofilm and as free bacteria, often doing so in less than 30 min. As such, these antimicrobials have the potential to alleviate the burden that Staphylococcus infections have on the health care system and cause better outcomes for infected patients.
Insights
Antimicrobial peptoids offer a promising alternative to conventional antibiotics for treating Staphylococcus aureus wound infections. These novel compounds rapidly kill both susceptible and resistant bacteria, including biofilms, with minimal side effects.
Area of Science:
- Synthetic biology and medicinal chemistry
- Antimicrobial drug discovery
- Wound infection treatment
Background:
- Staphylococcus aureus is a common cause of wound infections.
- Antibiotic resistance (methicillin and vancomycin) limits current treatment efficacy.
- Recalcitrant infections and biofilm formation pose significant challenges.
Purpose of the Study:
- To evaluate antimicrobial peptoids as an alternative to conventional antibiotics.
- To assess peptoid efficacy against methicillin-susceptible S. aureus (MSSA) and methicillin-resistant S. aureus (MRSA).
- To investigate peptoid activity against bacterial biofilms and in a wound infection model.
Main Methods:
- Design and synthesis of sequence-specific poly-N-substituted glycine peptoids mimicking host defense peptides.
- In vitro testing for bacterial killing kinetics and concentration (low micromolar).
- Assessment of cytotoxic effects in vivo.
- Evaluation of peptoid effects on biofilm formation and detachment.
- Utilized a bioluminescent S. aureus murine incision wound model.
Main Results:
- Peptoids demonstrated rapid (<30 min) and efficient killing of MSSA and MRSA at low micromolar concentrations.
- No apparent cytotoxic side effects were observed in vivo.
- Peptoids effectively prevented biofilm formation and detached existing biofilms (e.g., Peptoid 1 at 1.6 μM).
- Conventional antibiotics failed to prevent or detach biofilms.
- Peptoid treatment led to clearance of infection in a murine wound model within 8 days.
Conclusions:
- Antimicrobial peptoids show significant potential for treating S. aureus wound infections.
- Peptoids offer advantages over conventional antibiotics, including broad-spectrum activity, rapid killing, and anti-biofilm properties.
- These findings suggest peptoids could alleviate the healthcare burden of resistant S. aureus infections.
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