Liu Deyu, Li Chunyan, Cao Ting, Lv Xiuli, Yue Yingxue, Li Shuang, Cheng Yang, Liu Fei, Huo Guicheng, Li Bailiang
Key Laboratory of Dairy Science, Ministry of Education, Northeast Agricultural University, Harbin 150030, China.
Food College, Northeast Agricultural University, Harbin 150030, China.
Nutrients. 2024 Apr 13;16(8):1164. doi: 10.3390/nu16081164.
Enterohemorrhagic (EHEC) serotype O157:H7 is a commonly encountered foodborne pathogen that can cause hemorrhagic enteritis and lead to hemolytic uremic syndrome (HUS) in severe cases. is a beneficial bacterium that naturally exists in the human gut and plays a vital role in maintaining a healthy balance in the gut microbiota. This study investigated the protective effects of K5 in a mouse model of EHEC O157:H7 infection. The results indicated that pretreatment with K5 mitigated the clinical symptoms of EHEC O157:H7 infection and attenuated the increase in myeloperoxidase (MPO) activity in the colon of the mice. In comparison to the model group, elevated serum D-lactic acid concentrations and diamine oxidase (DAO) levels were prevented in the K5-EHEC group of mice. The reduced mRNA expression of tight junction proteins (ZO-1, Occludin, and Claudin-1) and mucin MUC2, as well as the elevated expression of virulence factors Stx1A and Stx2A, was alleviated in the colon of both the K5-PBS and K5-EHEC groups. Additionally, the increase in the inflammatory cytokine levels of TNF-α and IL-1β was inhibited and the production of IL-4 and IL-10 was promoted in the K5-EHEC group compared with the model group. K5 significantly prevented the reduction in the abundance and diversity of mouse gut microorganisms induced by EHEC O157:H7 infection, including blocking the decrease in the relative abundance of and Meanwhile, the intervention with K5 promoted the production of acetic acid and butyric acid in the gut. This study provides insights into the use of K5 for developing probiotic formulations to prevent intestinal diseases caused by pathogenic bacterial infections.
肠出血性大肠杆菌(EHEC)O157:H7是一种常见的食源性病原体,可引起出血性肠炎,严重时可导致溶血尿毒综合征(HUS)。[此处原文有缺失信息]是一种有益细菌,自然存在于人体肠道中,在维持肠道微生物群的健康平衡方面发挥着至关重要的作用。本研究在EHEC O157:H7感染的小鼠模型中研究了[此处原文有缺失信息]K5的保护作用。结果表明,用[此处原文有缺失信息]K5预处理可减轻EHEC O157:H7感染的临床症状,并减弱小鼠结肠中髓过氧化物酶(MPO)活性的增加。与模型组相比,[此处原文有缺失信息]K5-EHEC组小鼠的血清D-乳酸浓度和二胺氧化酶(DAO)水平升高得到了预防。紧密连接蛋白(ZO-1、闭合蛋白和Claudin-1)和粘蛋白MUC2的mRNA表达降低,以及毒力因子Stx1A和Stx2A的表达升高,在[此处原文有缺失信息]K5-PBS组和[此处原文有缺失信息]K5-EHEC组的结肠中均得到缓解。此外,与模型组相比,[此处原文有缺失信息]K5-EHEC组中促炎细胞因子TNF-α和IL-1β水平的升高受到抑制,IL-4和IL-10的产生得到促进。[此处原文有缺失信息]K5显著预防了EHEC O157:H7感染引起的小鼠肠道微生物丰度和多样性的降低,包括阻止[此处原文有缺失信息]和[此处原文有缺失信息]相对丰度的下降。同时,用[此处原文有缺失信息]K5进行干预促进了肠道中乙酸和丁酸的产生。本研究为利用[此处原文有缺失信息]K5开发益生菌制剂以预防由病原菌感染引起的肠道疾病提供了见解。