期刊
JOURNAL OF BIOSCIENCE AND BIOENGINEERING
卷 126, 期 1, 页码 30-37出版社
SOC BIOSCIENCE BIOENGINEERING JAPAN
DOI: 10.1016/j.jbiosc.2018.01.016
关键词
Persister; ldhA; Escherichia colt; Single cell; Microfiuidic device; Stochastic expression; Energy metabolism; Proton motive force
资金
- Japan Society for Promotion of Sciences (JSPS) [15K15134]
- Grants-in-Aid for Scientific Research [15K15134] Funding Source: KAKEN
Bacterial persisters are phenotypic variants that survive the treatment of lethal doses of growth-targeting antibiotics without mutations. Although the mechanism underlying persister formation has been studied for decades, how the persister phenotype is switched on and protects itself from antibiotics has been elusive. In this study, we focused on the lactate dehydrogenase gene (IdhA) that was upregulated in an Escherichia coli persister-enriched population. A survival rate assay using an ldhA-overexpressing strain showed that IdhA expression induced persister formation. To identify IdhA-mediated persister formation at the single-cell level, time-lapse microscopy with a microfluidic device was used. Stochastic IdhA expression was found to induce dormancy and tolerance against high-dose ampicillin treatment (500 mu g/ml). To better understand the underlying mechanism, we investigated the relationship between IdhA-mediated persister formation and previously reported persister formation through aerobic metabolism repression. As a result, IdhA expression enhanced the proton motive force (PMF) and ATP synthesis. These findings suggest that ldhA-mediated persister formation pathway is different from previously reported persister formation via repression of aerobic metabolism. (C) 2018, The Society for Biotechnology, Japan. All rights reserved.
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