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Vancomycin-resistant enterococci exploit antibiotic-induced innate immune deficits

机译:耐万古霉素的肠球菌利用抗生素诱导的先天性免疫缺陷

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Infection with antibiotic-resistant bacteria, such as vancomycin-resistant Enterococcus (VRE), is a dangerous and costly complication of broad-spectrum antibiotic therapy. How antibiotic-mediated elimination of commensal bacteria promotes infection by antibiotic-resistant bacteria is a fertile area for speculation with few defined mechanisms. Here we demonstrate that antibiotic treatment of mice notably downregulates intestinal expression of ReglHy (also known as Reg3g), a secreted C-type lectin that kills Gram-positive bacteria, including VRE. Downregulation of RegIIIγ markedly decreases in vivo killing of VRE in the intestine of antibiotic-treated mice. Stimulation of intestinal Toll-like receptor 4 by oral administration of lipopolysaccharide re-induces RegIIIγ, thereby boosting innate immune resistance of antibiotic-treated mice against VRE. Compromised mucosal innate immune defence, as induced by broad-spectrum antibiotic therapy, can be corrected by selectively stimulating mucosal epithelial Toll-like receptors, providing a potential therapeutic approach to reduce colonization and infection by antibiotic-resistant microbes.
机译:感染抗生素的细菌,例如耐万古霉素的肠球菌(VRE),是广谱抗生素治疗的危险且代价高昂的并发症。抗生素介导的共生细菌的消除如何促进抗生素抗性细菌的感染,是利用很少的确定机制进行推测的沃土。在这里,我们证明了对小鼠的抗生素治疗显着下调了ReglHy(也称为Reg3g)的肠道表达,ReglHy是一种分泌的C型凝集素,可以杀死包括VRE在内的革兰氏阳性细菌。 RegIIIγ的下调显着降低了用抗生素治疗的小鼠肠道对VRE的体内杀伤作用。通过口服脂多糖刺激小肠Toll样受体4可重新诱导RegIIIγ,从而增强经抗生素治疗的小鼠对VRE的先天免疫抵抗力。通过选择性刺激粘膜上皮Toll样受体,可以纠正广谱抗生素治疗所致的粘膜固有免疫防御能力下降,从而提供一种潜在的治疗方法,以减少对抗生素耐药的微生物的定植和感染。

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