氧化还原通过降低活性氧清除能力负向调节大肠杆菌O157:H7的加工应激抗性。

IF 3.5 3区 医学 Q3 IMMUNOLOGY
Na Lü, Zhengrong Yang, Chenglin Du, Jiaye Wan, Jingsheng Gan, Ziyi Zhang, Yajing Kong, Hui Yang, Xiaolin Cai, Shuhao Zeng, Chao Shi
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引用次数: 0

摘要

大肠杆菌O157:H7具有承受各种环境压力的能力,使其成为食品工业根除的重大挑战和对食品安全的威胁。本研究考察了氧还原对大肠杆菌O157:H7抗环境胁迫能力的影响。首先构建大肠杆菌O157:H7的oxyR敲除、互补和过表达菌株,分析野生菌株和突变菌株在酸、热、氧化和渗透胁迫条件下的存活情况。综上所述,在本实验条件下,氧还原主要调节大肠杆菌O157:H7对氧化应激的抗性,对其抗渗透胁迫能力影响较小,不影响其抗酸胁迫和热胁迫能力。通过测定氧化应激下4种菌株的ROS、MDA水平、细胞膜损伤和抗氧化酶活性,分析氧化r在抗氧化应激中的作用。结果表明,氧还原基因缺失使活性氧浓度降低54.00±1.24%,氧还原基因过表达菌株的MDA含量升高至0.78±0.03 nmol/mL,氧还原基因过表达菌株对细胞膜的损伤更为严重(轻度损伤为67.83±1.22%,重度损伤为28.88±1.13%),SOD、CAT和GSH-Px活性显著降低(P < 0.05)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The oxyR negatively regulates processing stress resistance in Escherichia coli O157:H7 by reducing ROS scavenging capacity.

Escherichia coli O157:H7 has the ability to withstand a wide range of environmental stresses, making it a major challenge to eradicate in the food industry and a threat to food safety. In this study, the effect of oxyR on the ability of E. coli O157:H7 to resist environmental stress was investigated. Firstly, oxyR knockout, complementation and overexpression strains of E. coli O157:H7 were constructed and analysed the survival of wild and mutant strains under conditions of acid, heat, oxidative and osmotic stress. The findings indicate that under the conditions of this experiment, oxyR mainly regulated the resistance of E. coli O157:H7 to oxidative stress, with less effect on the ability to resist osmotic stress, and did not affect the acid stress resistance and heat stress resistance. The role of oxyR in antioxidant stress was then analysed by assessing ROS, MDA levels, cell membrane damage and antioxidant enzyme activities in the four strains under oxidative stress. The results showed that the deletion of gene oxyR reduced the ROS concentration by 54.00±1.24%, the MDA content of oxyR overexpression strain increased to 0.78±0.03 nmol/mL, the overexpression of gene oxyR suffered more severe cell membrane damage (67.83±1.22% for minor damage and 28.88±1.13% for severe damage), and a significant decrease in the activities of SOD, CAT, and GSH-Px (P<0.05), as compared with the wild strain. This study suggests that oxyR regulates bacterial resistance to oxidative stress by affecting intracellular ROS, cell membrane integrity and antioxidant enzyme activities.

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来源期刊
Microbial pathogenesis
Microbial pathogenesis 医学-免疫学
CiteScore
7.40
自引率
2.60%
发文量
472
审稿时长
56 days
期刊介绍: Microbial Pathogenesis publishes original contributions and reviews about the molecular and cellular mechanisms of infectious diseases. It covers microbiology, host-pathogen interaction and immunology related to infectious agents, including bacteria, fungi, viruses and protozoa. It also accepts papers in the field of clinical microbiology, with the exception of case reports. Research Areas Include: -Pathogenesis -Virulence factors -Host susceptibility or resistance -Immune mechanisms -Identification, cloning and sequencing of relevant genes -Genetic studies -Viruses, prokaryotic organisms and protozoa -Microbiota -Systems biology related to infectious diseases -Targets for vaccine design (pre-clinical studies)
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