Author:
Zou Zongsen,Obernuefemann Chloe L. P.,Singh Pardeep,Pinkner Jerome S.,Xu Wei,Nye Taylor M.,Dodson Karen W.,Almqvist Fredrik,Hultgren Scott J.,Caparon Michael G.
Abstract
ABSTRACTWe have developed GmPcides from a peptidomimetic dihydrothiazolo ring-fused 2-pyridone scaffold that have antimicrobial activities against a broad-spectrum of Gram-positive pathogens. Here we examine the treatment efficacy of GmPcides using skin and soft tissue infection (SSTI) and biofilm formation models byStreptococcus pyogenes. Screening our compound library for minimal inhibitory (MIC) and minimal bactericidal (MBC) concentrations identified GmPcide PS757 as highly active againstS. pyogenes. Treatment ofS. pyogenesbiofilm with PS757 revealed robust efficacy against all phases of biofilm formation by preventing initial biofilm development, ceasing biofilm maturation and eradicating mature biofilm. In a murine model ofS. pyogenesSSTI, subcutaneous delivery of PS757 resulted in reduced levels of tissue damage, decreased bacterial burdens and accelerated rates of wound-healing, which were associated with down-regulation of key virulence factors, including M protein and the SpeB cysteine protease. These data demonstrate that GmPcides show considerable promise for treatingS. pyogenesinfections.
Publisher
Cold Spring Harbor Laboratory