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11168H 接触青霉素后形成持留细胞和氧化还原蛋白活性改变的细胞。

11168H Exposed to Penicillin Forms Persister Cells and Cells With Altered Redox Protein Activity.

机构信息

College of Life and Environmental Sciences-Biosciences, University of Exeter, Exeter, United Kingdom.

School of Life Sciences, University of Warwick, Coventry, United Kingdom.

出版信息

Front Cell Infect Microbiol. 2020 Oct 19;10:565975. doi: 10.3389/fcimb.2020.565975. eCollection 2020.

Abstract

The formation of persister cells is one mechanism by which bacteria can survive exposure to environmental stresses. We show that 11168H forms persister cells at a frequency of 10 after exposure to 100 × MIC of penicillin G for 24 h. Staining the cell population with a redox sensitive fluorescent dye revealed that penicillin G treatment resulted in the appearance of a population of cells with increased fluorescence. We present evidence, to show this could be a consequence of increased redox protein activity in, or associated with, the electron transport chain. These data suggest that a population of penicillin G treated cells could undergo a remodeling of the electron transport chain in order to moderate membrane hyperpolarization and intracellular alkalization; thus reducing the antibiotic efficacy and potentially assisting in persister cell formation.

摘要

形成持留细胞是细菌能够在暴露于环境应激时存活的一种机制。我们表明,11168H 在暴露于 100×MIC 的青霉素 G 24 小时后,以 10 的频率形成持留细胞。用氧化还原敏感荧光染料对细胞群体进行染色表明,青霉素 G 处理导致具有增加荧光的细胞群体的出现。我们提出证据表明,这可能是电子传递链中或与之相关的氧化还原蛋白活性增加的结果。这些数据表明,青霉素 G 处理的细胞群体可能会对电子传递链进行重塑,以减轻膜超极化和细胞内碱化;从而降低抗生素的疗效,并可能有助于持留细胞的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad5e/7641608/65d7c6d5beeb/fcimb-10-565975-g0001.jpg

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