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一氧化氮代谢酶在拮抗肠出血性大肠杆菌中硝化应激的协同作用

Cooperative Roles of Nitric Oxide-Metabolizing Enzymes To Counteract Nitrosative Stress in Enterohemorrhagic Escherichia coli.

机构信息

Department of Molecular Infectiology, Graduate School of Medicine, Chiba University, Chiba, Japan

Department of Aging Pharmacology, School of Medicine, Toho University, Tokyo, Japan.

出版信息

Infect Immun. 2019 Aug 21;87(9). doi: 10.1128/IAI.00334-19. Print 2019 Sep.

Abstract

Enterohemorrhagic (EHEC) has at least three enzymes, NorV, Hmp, and Hcp, that act independently to lower the toxicity of nitric oxide (NO), a potent antimicrobial molecule. This study aimed to reveal the cooperative roles of these defensive enzymes in EHEC against nitrosative stress. Under anaerobic conditions, combined deletion of all three enzymes significantly increased the NO sensitivity of EHEC determined by the growth at late stationary phase; however, the expression of restored the NO resistance of EHEC. On the other hand, the growth of Δ mutant EHEC was inhibited after early stationary phase, indicating that NorV and Hmp play a cooperative role in anaerobic growth. Under microaerobic conditions, the growth of Δ mutant EHEC was inhibited by NO, indicating that Hmp is the enzyme that protects cells from NO stress under microaerobic conditions. When EHEC cells were exposed to a lower concentration of NO, the NO level in bacterial cells of Δ mutant EHEC was higher than those of the other EHEC mutants, suggesting that Hcp is effective at regulating NO levels only at a low concentration. These findings of a low level of NO in bacterial cells with indicate that the NO consumption activity of Hcp was suppressed by Hmp at a low range of NO concentrations. Taken together, these results show that the cooperative effects of NO-metabolizing enzymes are regulated by the range of NO concentrations to which the EHEC cells are exposed.

摘要

肠出血性大肠杆菌 (EHEC) 至少有三种酶,即 NorV、Hmp 和 Hcp,它们独立作用以降低一氧化氮 (NO) 的毒性,NO 是一种有效的抗菌分子。本研究旨在揭示这些防御性酶在 EHEC 对抗硝化应激中的协同作用。在厌氧条件下,三种酶的联合缺失显著增加了晚期停滞期生长时 EHEC 对 NO 的敏感性;然而,的表达恢复了 EHEC 对 NO 的抗性。另一方面,Δ突变体 EHEC 的生长在早期停滞期后受到抑制,表明 NorV 和 Hmp 在厌氧生长中发挥协同作用。在微需氧条件下,NO 抑制了 Δ突变体 EHEC 的生长,表明 Hmp 是在微需氧条件下保护细胞免受 NO 应激的酶。当 EHEC 细胞暴露于较低浓度的 NO 时,Δ突变体 EHEC 中细菌细胞内的 NO 水平高于其他 EHEC 突变体,表明 Hcp 仅在低浓度时有效调节 NO 水平。这些发现表明,在低浓度的 NO 下,细菌细胞内的 NO 水平较低,这表明 Hcp 的 NO 消耗活性在低浓度的 NO 范围内受到 Hmp 的抑制。综上所述,这些结果表明,NO 代谢酶的协同作用受 EHEC 细胞暴露的 NO 浓度范围的调节。

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