| Literature DB >> 29569952 |
Wooseong Kim1, Gabriel L Hendricks1, Katerina Tori1, Beth B Fuchs1, Eleftherios Mylonakis1.
Abstract
Chronic Staphylococcus aureus infections are complicated by frequent relapses not only from the development of drug resistance to conventional antibiotics, but also through the formation of persister bacterial cells. Bacterial persisters are in a transient, metabolically inactive state, making conventional antibiotics that target essential cellular growth processes ineffective, resulting in high clinical failure rates of antibiotic chemotherapy. The development of new antibiotics against persistent S. aureus is an urgent issue. Over the last decade, new strategies to identify S. aureus persister-active compounds have been proposed. This review summarizes the proposed targets, antipersister compounds and innovative methods that may augment conventional antibiotics against S. aureus persisters. The reviewed antipersister strategies can be summarized as two broad categories; directly targeting growth-independent targets and potentiating existing, ineffective antibiotics by aiding uptake or accessibility.Entities:
Keywords: MRSA; antibiotics; drug discover; persisters
Mesh:
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Year: 2018 PMID: 29569952 PMCID: PMC6077763 DOI: 10.4155/fmc-2017-0199
Source DB: PubMed Journal: Future Med Chem ISSN: 1756-8919 Impact factor: 3.808