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首页> 外文期刊>Scientific reports. >Cathelicidin- derived PR39 protects enterohemorrhagic Escherichia coli O157:H7 challenged mice by improving epithelial function and balancing the microbiota in the intestine
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Cathelicidin- derived PR39 protects enterohemorrhagic Escherichia coli O157:H7 challenged mice by improving epithelial function and balancing the microbiota in the intestine

机译:通过改善上皮函数并平衡肠道的微生物来保护肠溶病大肠杆菌O157:H7面临攻击的小鼠的肠溶性蛋白蛋白 - 衍生的PR39

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The zoonotic enterohaemorrhagic Escherichia coli (EHEC) O157:H7 can disrupt intestinal epithelial barrier function and in turn leading to serious intestinal and systemic disease. PR39 could effectively inhibit the growth of Gram-negative bacteria, but there is little knowledge of its effects on intestinal barrier function and the microbiota in E. coli-challenged mice. In this study, an intestinal disease caused by EHEC O157:H7 was established, to analyze the effect of PR39 on EHEC O157:H7 induced intestinal epithelial barrier injury and disorder. Interestingly, PR39 attenuated EHEC O157:H7-induced systemic symptoms and significantly decreased mortality and the degree of E. coli shedding in faeces. Furthermore, the infiltration index of macrophages and neutrophils in intestine of the PR39 treatment group were obviously attenuated, along with the level of apoptosis. PR39 treatment group had distinctly improved tight junction associated proteins' expression after EHEC O157:H7 caused injury. Additionally, the sequencing analysis of cecum microbiota showed that PR39 altered the abnormal increase in Bacteroides caused by EHEC O157:H7 and promoted the growth of probiotics such as Lactobacillus. In conclusion, cathelicidin-derived PR39 could effectively improve EHEC O157:H7-induced epithelial barrier injury, and dysfunction of immune and microbiota homeostasis in the intestinal tract, indicating that PR39 could be an excellent potential drug for zoonotic EHEC O157:H7-related intestinal disease.
机译:胃肠病肠杆菌大肠杆菌(EHEC)O157:H7可以破坏肠上皮屏障功能,导致严重的肠道和全身疾病。 PR39可以有效抑制革兰氏阴性细菌的生长,但对其对大肠杆菌攻击小鼠的肠道屏障功能和微生物生物的影响几乎没有了解。在这项研究中,建立了由EHEC O157:H7引起的肠病,分析PR39对EHEC O157:H7诱导的肠上皮阻挡损伤和病症的影响。有趣的是,PR39减毒了EHEC O157:H7诱导的全身症状,大大降低了粪便中的死亡率和大肠杆菌的程度。此外,PR39治疗组肠道中巨噬细胞和中性粒细胞的浸润指数明显衰减,以及细胞凋亡的水平。在EHEC O157后,PR39治疗组在eHEC O157:H7造成的伤害后明显改善了紧密结合的蛋白质表达。另外,盲肠微生物群的测序分析表明,PR39改变了由EHEC O157:H7引起的菌体异常增加,并促进益生菌如乳杆菌的生长。总之,Cathelicidin衍生的PR39可以有效地改善EHEC O157:H7诱导的上皮阻隔损伤,并且免疫和微生物生物血症在肠道中的功能障碍,表明PR39可能是一种优秀的潜在药物,用于eHEC O157:H7相关肠道疾病。

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