| Literature DB >> 30132650 |
Wooseong Kim1, Andrew D Steele2, Wenpeng Zhu3, Erika E Csatary2, Nico Fricke3, Madeline M Dekarske2, Elamparithi Jayamani1, Wen Pan1, Bumsup Kwon4, Isabelle F Sinitsa5, Jake L Rosen2, Annie L Conery6,7, Beth Burgwyn Fuchs1, Petia M Vlahovska8, Frederick M Ausubel6,7, Huajian Gao3, William M Wuest2, Eleftherios Mylonakis1.
Abstract
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.Entities:
Keywords: MD simulations; MRSA; SAR; antibiotics; membrane-active agent; persisters
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Year: 2018 PMID: 30132650 PMCID: PMC6468991 DOI: 10.1021/acsinfecdis.8b00161
Source DB: PubMed Journal: ACS Infect Dis ISSN: 2373-8227 Impact factor: 5.084