Roth Myriam, Jaquet Vincent, Lemeille Sylvain, Bonetti Eve-Julie, Cambet Yves, François Patrice, Krause Karl-Heinz
Department of Pathology and Immunology, Medical School, University of Geneva, 1211 Geneva, Switzerland.
REaders, Assay Development & Screening Unit (READS Unit), Faculty of Medecine, University of Geneva, 1211 Geneva, Switzerland.
Antioxidants (Basel). 2022 Mar 28;11(4):655. doi: 10.3390/antiox11040655.
Hydrogen peroxide (HO) is a key defense component of host-microbe interaction. However, HO concentrations generated by immune cells or epithelia are usually insufficient for bacterial killing and rather modulate bacterial responses. Here, we investigated the impact of sublethal HO concentration on gene expression of BW25113 after 10 and 60 min of exposure. RNA-seq analysis revealed that approximately 12% of bacterial genes were strongly dysregulated 10 min following exposure to 2.5 mM HO. HO exposure led to the activation of a specific antioxidant response and a general stress response. The latter was characterized by a transient down-regulation of genes involved in general metabolism, such as nucleic acid biosynthesis and translation, with a striking and coordinated down-regulation of genes involved in ribosome formation, and a sustained up-regulation of the SOS response. We confirmed the rapid transient and specific response mediated by the transcription factor OxyR leading to up-regulation of antioxidant systems, including the catalase-encoding gene (), that rapidly degrade extracellular HO and promote bacterial survival. We documented a strong and transient up-regulation of genes involved in sulfur metabolism and cysteine biosynthesis, which are under the control of the transcription factor CysB. This strong specific transcriptional response to HO exposure had no apparent impact on bacterial survival, but possibly replenishes the stores of oxidized cysteine and glutathione. In summary, our results demonstrate that different stress response mechanisms are activated by HO exposure and highlight the cysteine synthesis as an antioxidant response in .
过氧化氢(H₂O₂)是宿主-微生物相互作用中的关键防御成分。然而,免疫细胞或上皮细胞产生的H₂O₂浓度通常不足以杀死细菌,反而会调节细菌的反应。在此,我们研究了亚致死浓度的H₂O₂在暴露10分钟和60分钟后对BW25113基因表达的影响。RNA测序分析显示,在暴露于2.5 mM H₂O₂ 10分钟后,约12%的细菌基因发生了强烈的失调。H₂O₂暴露导致特定抗氧化反应和一般应激反应的激活。后者的特征是参与一般代谢的基因,如核酸生物合成和翻译相关基因的短暂下调,核糖体形成相关基因的显著且协同下调,以及SOS反应的持续上调。我们证实了转录因子OxyR介导的快速瞬时和特异性反应,导致抗氧化系统上调,包括过氧化氢酶编码基因(),该基因可快速降解细胞外H₂O₂并促进细菌存活。我们记录了参与硫代谢和半胱氨酸生物合成的基因的强烈且瞬时上调,这些基因受转录因子CysB的控制。这种对H₂O₂暴露的强烈特异性转录反应对细菌存活没有明显影响,但可能补充了氧化型半胱氨酸和谷胱甘肽的储备。总之,我们的结果表明,H₂O₂暴露激活了不同的应激反应机制,并突出了半胱氨酸合成作为大肠杆菌中的一种抗氧化反应。