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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 779-794 |
| Number of pages | 16 |
| Journal | Future Medicinal Chemistry |
| Volume | 10 |
| Issue number | 7 |
| DOIs | |
| State | Published - Apr 2018 |
Keywords
- MRSA
- antibiotics
- drug discover
- persisters
ASJC Scopus subject areas
- Molecular Medicine
- Pharmacology
- Drug Discovery
Divisions
- Infectious Disease
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