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Pro-inflammatory potential of Escherichia coli strains K12and Nissle 1917 in a murine model of acute ileitis

机译:大肠杆菌K12菌株的促炎潜力和Nissle 1917在急性回肠炎的小鼠模型中

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摘要

Non-pathogenic Escherichia coli (Ec) strains K12 (EcK12) and Nissle 1917 (EcN) are used for gene technology and probiotic treatment of intestinal inflammation, respectively. We investigated intestinal colonization and potential pro-inflammatory properties of EcK12, EcN, and commensal E. coli (EcCo) strains in Toxoplasma (T.) gondii-induced acute ileitis. Whereas gnotobiotic animals generated by quintuple antibiotic treatment were protected from ileitis, mice replenished with conventional microbiota suffered from small intestinal necrosis 7 days post-T. gondii infection (p.i.). Irrespective of the Ec strain, recolonized mice revealed mild to moderate histopathological changes in their ileal mucosa. Upon stable recolonization with EcK12, EcN, or EcCo, development of inflammation was accompanied by pro-inflammatory responses at day 7 p.i., including increased ileal T lymphocyte and apoptotic cell numbers compared to T. gondii-infected gnotobiotic controls. Strikingly, either Ec strain was capable to translocate to extra-intestinal locations, such as MLN, spleen, and liver. Taken together, Ec strains used in gene technology and probiotic treatment are able to exert inflammatory responses in a murine model of small intestinal inflammation. In conclusion, the therapeutic use of Ec strains in patients with broad-spectrum antibiotic treatment and/or intestinalinflammation should be considered with caution.
机译:非致病性大肠杆菌(Ec)菌株K12(EcK12)和Nissle 1917(EcN)分别用于基因技术和肠道细菌的益生菌治疗。我们调查了弓形虫(T.)弓形虫诱发的急性回肠炎中EcK12,EcN和共生大肠杆菌(EcCo)菌株的肠道定殖和潜在的促炎特性。尽管通过五重抗生素治疗产生的可生生物动物受到了回肠炎的保护,但补充了常规微生物群的小鼠在T后7天遭受小肠坏死。刚地感染(p.i.)。不论Ec株,重新定殖的小鼠在回肠粘膜中均显示出轻度至中度的组织病理学变化。在与EcK12,EcN或EcCo进行稳定的再定殖后,炎症的发展在p.i. 7天伴随着促炎反应,包括与刚地弓形虫感染的致病菌对照相比,回肠T淋巴细胞和凋亡细胞数量增加。令人惊讶的是,任一Ec菌株都能够转移到肠外位置,例如MLN,脾脏和肝脏。总之,用于基因技术和益生菌治疗的Ec菌株能够在小肠炎症的鼠模型中发挥炎症反应。总之,Ec菌株在广谱抗生素治疗和/或肠道治疗中的治疗用途炎症应慎重考虑。

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