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首页> 外文期刊>Infection and immunity >Concurrent Infection with an Intestinal Helminth Parasite Impairs Host Resistance to Enteric Citrobacter rodentium and Enhances Citrobacter-Induced Colitis in Mice
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Concurrent Infection with an Intestinal Helminth Parasite Impairs Host Resistance to Enteric Citrobacter rodentium and Enhances Citrobacter-Induced Colitis in Mice

机译:肠道蠕虫寄生虫的并发感染会损害宿主对肠道柠檬酸杆菌的抵抗力,并增强小鼠柠檬酸杆菌诱导的结肠炎。

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Infections with intestinal helminth and bacterial pathogens, such as enteropathogenic Escherichia coli, continue to be a major global health threat for children. To test the hypothesis that intestinal helminth infection may be a risk factor for enteric bacterial infection, a murine model was established by using the intestinal helminth Heligomosomoides polygyrus. To analyze the modulatory effect of a Th2-inducing helminth on the outcome of enteric bacterium Citrobacter rodentium infection, BALB/c and STAT 6 knockout (KO) mice were infected with H. polygyrus, C. rodentium, or both. We found that only BALB/c mice coinfected with H. polygyrus and C. rodentium displayed a marked morbidity and mortality. The enhanced susceptibility to C. rodentium and intestinal injury of coinfected BALB/c mice were shown to be associated with a significant increase in helminth-driven Th2 responses, mucosally and systemically, and correlated with a significant downregulation of protective gamma interferon and with a dramatic upregulation of the proinflammatory tumor necrosis factor alpha response. In addition, C. rodentium-associated colonic pathology in coinfected BALB/c mice was significantly enhanced, whereas bacterial burden was increased and clearance was delayed. In contrast, coinfection in STAT 6 KO mice failed to promote C. rodentium infection or to induce a more severe intestinal inflammation and tissue injury, demonstrating a mechanism by which helminth influences the development of host protective immunity and susceptibility to bacterial infections. We conclude that H. polygyrus coinfection can promote C. rodentium-associated disease and colitis through a STAT 6-mediated immune mechanism.
机译:肠道蠕虫和细菌性病原体的感染,例如肠致病性大肠埃希氏大肠杆菌,仍然是对儿童健康的主要全球威胁。为了检验肠道蠕虫感染可能是肠道细菌感染的危险因素的假设,通过使用肠道蠕虫 Heligomosomoides polygyrus 建立了小鼠模型。为了分析诱导Th2的蠕虫对肠细菌 Citrobacter rodentium 感染结果的调节作用,将BALB / c和STAT 6基因敲除(KO)小鼠感染了 H。一夫多妻制 C。啮齿动物,或两者兼有。我们发现只有BALB / c小鼠与 H共感染。一夫多妻制 C。啮齿动物显示出明显的发病率和死亡率。对 C的敏感性增加。合并感染的BALB / c小鼠的啮齿类动物和肠损伤与蠕虫驱动的Th2反应(黏膜和全身)显着增加有关,与保护性γ干扰素的显着下调相关,并且与γ-干扰素的显着上调相关促炎性肿瘤坏死因子α反应。此外, C。合并感染的BALB / c小鼠中与啮齿类动物有关的结肠病理显着增强,而细菌负荷增加,清除延迟。相反,STAT 6 KO小鼠中的合并感染未能促进C。或感染更严重的肠道炎症和组织损伤,证明蠕虫可通过这种机制影响宿主保护性免疫的发展和对细菌感染的敏感性。我们得出结论, H。 polygyrus 共感染可以促进 C。 STAT 6介导的免疫机制与啮齿类动物相关的疾病和结肠炎。

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