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Enhanced Efflux Activity Facilitates Drug Tolerance in Dormant Bacterial Cells.


ABSTRACT: Natural variations in gene expression provide a mechanism for multiple phenotypes to arise in an isogenic bacterial population. In particular, a sub-group termed persisters show high tolerance to antibiotics. Previously, their formation has been attributed to cell dormancy. Here we demonstrate that bacterial persisters, under ?-lactam antibiotic treatment, show less cytoplasmic drug accumulation as a result of enhanced efflux activity. Consistently, a number of multi-drug efflux genes, particularly the central component TolC, show higher expression in persisters. Time-lapse imaging and mutagenesis studies further establish a positive correlation between tolC expression and bacterial persistence. The key role of efflux systems, among multiple biological pathways involved in persister formation, indicates that persisters implement a positive defense against antibiotics prior to a passive defense via dormancy. Finally, efflux inhibitors and antibiotics together effectively attenuate persister formation, suggesting a combination strategy to target drug tolerance.

SUBMITTER: Pu Y 

PROVIDER: S-EPMC4850422 | biostudies-other | 2016 Apr

REPOSITORIES: biostudies-other

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Enhanced Efflux Activity Facilitates Drug Tolerance in Dormant Bacterial Cells.

Pu Yingying Y   Zhao Zhilun Z   Li Yingxing Y   Zou Jin J   Ma Qi Q   Zhao Yanna Y   Ke Yuehua Y   Zhu Yun Y   Chen Huiyi H   Baker Matthew A B MAB   Ge Hao H   Sun Yujie Y   Xie Xiaoliang Sunney XS   Bai Fan F  

Molecular cell 20160401 2


Natural variations in gene expression provide a mechanism for multiple phenotypes to arise in an isogenic bacterial population. In particular, a sub-group termed persisters show high tolerance to antibiotics. Previously, their formation has been attributed to cell dormancy. Here we demonstrate that bacterial persisters, under β-lactam antibiotic treatment, show less cytoplasmic drug accumulation as a result of enhanced efflux activity. Consistently, a number of multi-drug efflux genes, particula  ...[more]

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