Persistence and Culturability of Escherichia coli under Induced Toxin Expression

Yousr Dhaouadi, Mohamad Javad Hashemi, Dacheng Ren
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Abstract

Background/Objectives: Bacteria are well known to enter dormancy under stress conditions. However, the mechanisms of different dormancy-related phenotypes are still under debate and many questions remain unanswered. This study aims to better understand the effects of toxin gene expression on the dormancy of Escherichia coli. Methods: The effects of toxin gene expression on growth, persistence, and culturability were characterized. Specifically, we detailed dose- and time-dependent dormancy of E. coli and its susceptibility to ofloxacin via arabinose-induced hipA toxin gene expression under the PBAD promoter. A new plot was developed to better describe the dynamic changes in culturability and persistence. The expression level of hipA was determined using qPCR and cellular activities were monitored using fluorescence imaging and flow cytometry. Results: High-level persister formation and strong tolerance to ofloxacin were observed after high-level hipA induction. The new plot reveals more information than the changes in persistence alone, e.g., reduced culturability of E. coli and thus deeper dormancy under high-level hipA induction. Consistently, controlled hipA induction led to decreased cellular activities at promoter PrrnBP1 and an increase in the non-culturable subpopulation. Conclusions: Overall, this study provides new insights into dormancy induced by toxin gene expression and a more comprehensive view of persistence and culturability. The findings may help develop better control agents against dormant bacterial cells.
大肠杆菌在诱导毒素表达条件下的持久性和可培养性
背景/目的:众所周知,细菌在压力条件下会进入休眠状态。然而,不同休眠相关表型的机理仍存在争议,许多问题仍未得到解答。本研究旨在更好地了解毒素基因表达对大肠杆菌休眠的影响。研究方法研究表征了毒素基因表达对生长、持久性和可培养性的影响。具体来说,我们详细研究了大肠杆菌的剂量和时间依赖性休眠及其在 PBAD 启动子下通过阿拉伯糖诱导的 hipA 毒素基因表达对氧氟沙星的敏感性。为了更好地描述可培养性和持久性的动态变化,我们开发了一种新的图谱。使用 qPCR 测定了 hipA 的表达水平,并使用荧光成像和流式细胞术监测了细胞活性。结果显示在高水平的 hipA 诱导后,观察到了高水平的宿主形成和对氧氟沙星的强耐受性。新的图谱比单纯的持久性变化揭示了更多信息,例如,在高水平的 hipA 诱导下,大肠杆菌的可培养性降低,因此休眠更深。一致的是,受控的 hipA 诱导导致启动子 PrrnBP1 的细胞活性降低,不可培养亚群增加。结论总之,本研究为毒素基因表达诱导的休眠提供了新的见解,也为持久性和可培养性提供了更全面的视角。这些发现可能有助于开发出更好的控制休眠细菌细胞的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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