The emergence of multidrug-resistant microorganisms has been termed one of the most common global health threats, emphasizing the discovery of new antibacterial agents. To address this issue, we engineered peptides harboring "RWWWR" as a central motif plus arginine (R) end-tagging and then tested them in vitro and in vivo . Our results demonstrate that Pep 6, one of the engineered peptides, shows great potential in combating Escherichia coli bacteremia and the Staphylococcus aureus skin burn infection model, which induces a 62-90% reduction in bacterial burden. Remarkably, after long serial passages of S. aureus and E. coli for 30 days, Pep 6 is still highly efficient in killing pathogens, compared with 64- and 128-fold increase in minimal inhibitory concentrations (MICs) for vancomycin and polymyxin B, respectively. We also found that Pep 6 exhibited robust biofilm-inhibiting activity and eliminated 61.33% of the mature methicillin-resistant Staphylococcus aureus (MRSA) biofilm with concentration in the MIC level. These results suggest that the RWWWR motif and binding of arginine end-tagging could be harnessed as a new agent for combating multidrug-resistant bacteria.
Keyphrases
- methicillin resistant staphylococcus aureus
- multidrug resistant
- staphylococcus aureus
- gram negative
- highly efficient
- escherichia coli
- global health
- drug resistant
- biofilm formation
- klebsiella pneumoniae
- nitric oxide
- acinetobacter baumannii
- amino acid
- wound healing
- public health
- small molecule
- signaling pathway
- pseudomonas aeruginosa
- high throughput
- binding protein
- anti inflammatory
- human health
- transcription factor