Post-fluoroquinolone treatment molecular events and nutrient availability modulate Staphylococcus aureus antibiotic persistence

Staphylococcus aureus is an opportunistic bacterial pathogen that is associated with about one million deaths per year worldwide. S. aureus can infect a wide range of host sites including skin, bone, and the airway. At nutrient-limited infection sites, competition with immune cells can further deprive S. aureus of metabolites, including its preferred carbon sources, forcing the bacteria to enter into a state of reduced metabolic activity. While lower metabolic activity may help contain growth of the pathogen, it can also enhance S. aureus ’s survival during antibiotic treatment. Here, we focus on S. aureus ’s response to the fluoroquinolone (FQ) class of drugs, which inhibit topoisomerases necessary for nucleic acid synthesis and can lead to double-stranded DNA break (DSB) formation. We show that even in stationary phase, when nucleic acid synthesis levels are minimal, loss of DNA repair enzymes reduces S. aureus ’s FQ persistence. Using genetic and imaging approaches, we found that both persisters and cells that die induce DNA damage responses after FQ treatment terminates, and DNA repair enzymes are needed mainly during this recovery period. We found that starving S. aureus after treatment significantly increases FQ persistence, even in cells lacking the ability to repair DSBs. Our data suggest that starvation increases persistence by delaying the resumption of nucleic acid synthesis after treatment, allowing time for FQs to dissociate from trapped topoisomerases and be expelled from the cell. This study demonstrates that the nutritional environment and molecular events during post-FQ treatment recovery are crucial in determining the survival of S. aureus . Our findings point to processes that can be targeted to enhance the post-antibiotic effect and sensitize S. aureus to FQs to improve treatment outcomes.