Discovery and Optimization of nTZDpa as an Antibiotic Effective Against Bacterial Persisters.
Wooseong KimAndrew D SteeleWenpeng ZhuErika E CsataryNico FrickeMadeline M DekarskeElamparithi JayamaniWen PanBumsup KwonIsabelle F SinitsaJake L RosenAnnie L ConeryBeth Burgwyn FuchsPetia M VlahovskaFrederick M AusubelHuajian GaoWilliam M WuestEleftherios MylonakisPublished in: ACS infectious diseases (2018)
Conventional antibiotics are not effective in treating infections caused by drug-resistant or persistent nongrowing bacteria, creating a dire need for the development of new antibiotics. We report that the small molecule nTZDpa, previously characterized as a nonthiazolidinedione peroxisome proliferator-activated receptor gamma partial agonist, kills both growing and persistent Staphylococcus aureus cells by lipid bilayer disruption. S. aureus exhibited no detectable development of resistance to nTZDpa, and the compound acted synergistically with aminoglycosides. We improved both the potency and selectivity of nTZDpa against MRSA membranes compared to mammalian membranes by leveraging synthetic chemistry guided by molecular dynamics simulations. These studies provide key insights into the design of selective and potent membrane-active antibiotics effective against bacterial persisters.
Keyphrases
- drug resistant
- small molecule
- molecular dynamics simulations
- staphylococcus aureus
- multidrug resistant
- acinetobacter baumannii
- induced apoptosis
- methicillin resistant staphylococcus aureus
- protein protein
- molecular docking
- cell cycle arrest
- biofilm formation
- oxidative stress
- high throughput
- pseudomonas aeruginosa
- cystic fibrosis
- anti inflammatory
- candida albicans