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• W2083581925 abstract "Phenotypic variability in populations of cells has been linked to evolutionary robustness to stressful conditions. A remarkable example of the importance of cell-to-cell variability is found in bacterial persistence, where subpopulations of dormant bacteria, termed persisters, were shown to be responsible for the persistence of the population to antibiotic treatments. Here, we use microfluidic devices to monitor the induction of fluorescent proteins under synthetic promoters and characterize the dormant state of single persister bacteria. Surprisingly, we observe that protein production does take place in supposedly dormant bacteria, over a narrow time window after the exit from stationary phase. Only thereafter does protein production stop, suggesting that differentiation into persisters fully develops over this time window and not during starvation, as previously believed. In effect, we observe that exposure of bacteria to antibiotics during this time window significantly reduces persistence. Our results point to new strategies to fight persistent bacterial infections. The quantitative measurement of single-cell induction presented in this study should shed light on the processes leading to the dormancy of subpopulations in different systems, such as in subpopulations of viable but nonculturable bacteria, or those of quiescent cancer cells." @default.
• W2083581925 created "2016-06-24" @default.
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• W2083581925 date "2008-04-22" @default.
• W2083581925 modified "2023-10-16" @default.
• W2083581925 title "Single-cell protein induction dynamics reveals a period of vulnerability to antibiotics in persister bacteria" @default.
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• W2083581925 doi "https://doi.org/10.1073/pnas.0711712105" @default.
• W2083581925 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2329697" @default.
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