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Comparison of Tissue-Selective Proinflammatory Gene Induction in Mice Infected with Wild-Type, DNA Adenine Methylase-Deficient, and Flagellin-Deficient Salmonella enterica▿ †

机译:比较野生型,DNA腺嘌呤甲基化酶缺陷型和鞭毛蛋白缺陷型沙门氏菌感染小鼠的组织选择性促炎基因诱导†

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摘要

Mutants of Salmonella enterica serovar Typhimurium deficient in DNA adenine methylase (Dam) are attenuated for virulence in mice and confer heightened immunity in vaccinated animals. In contrast, infection of mice with wild-type (WT) strains or flagellin-deficient mutants of Salmonella causes typhoid fever. Here we examined the bacterial load and spatiotemporal kinetics of expression of several classes of host genes in Peyer's patches, the liver, and the spleen following oral infection of mice with WT, dam mutant, or flagellin-deficient (flhC) Salmonella. The genes evaluated included inflammatory (interleukin-1β [IL-1β], tumor necrosis factor alpha), chemokine (macrophage inflammatory protein 2), Th1/Th2 indicator (IL-12p40, IL-4), and interferon system (beta interferon [IFN-β], IFN-γ, protein Mx1 GTPase, RNA-dependent protein kinase, inducible nitric oxide synthase, suppressor of cytokine signaling 1) beacons. We showed that maximal interferon system and proinflammatory gene induction occurred by 5 days after infection and that the levels were comparable for the WT and flhC strains but were significantly lower for the dam mutant. Additionally, host gene expression in systemic tissues of individual animals was dependent on the bacterial load in the Peyer's patches for mice infected with WT, dam mutant, or flhC mutant Salmonella as early as 8 h after infection. Moreover, a bacterial load threshold in the Peyer's patches was necessary to stimulate the host gene induction in the liver and spleen. Taken together, these results suggest that bacterial load and the accompanying strain-specific cytokine signature are important determinants of the host innate immune response and associated disease manifestations observed in dam mutant Salmonella-infected animals compared to the immune response and disease manifestations observed in WT and flhC mutant Salmonella-infected animals.
机译:缺乏DNA腺嘌呤甲基化酶(Dam)的沙门氏菌血清型鼠伤寒沙门氏菌突变体可降低小鼠的毒力,并提高接种动物的免疫力。相反,用野生型(WT)菌株或沙门氏菌鞭毛蛋白缺陷型突变体感染小鼠会引起伤寒。在这里,我们研究了小鼠口服WT,dam突变体或鞭毛蛋白缺陷(flhC)沙门氏菌感染小鼠后,在派伊尔斑块,肝脏和脾脏中几种宿主基因表达的细菌负荷和时空动力学。评价的基因包括炎性基因(白介素-1β[IL-1β],肿瘤坏死因子α),趋化因子(巨噬细胞炎性蛋白2),Th1 / Th2指示剂(IL-12p40,IL-4)和干扰素系统(β干扰素[ IFN-β],IFN-γ,蛋白Mx1 GTPase,RNA依赖性蛋白激酶,诱导型一氧化氮合酶,细胞因子信号传导抑制剂1)信标。我们显示最大的干扰素系统和促炎基因诱导在感染后5天发生,并且该水平与WT和flhC菌株相当,但对于dam突变体则明显较低。另外,在感染后8 h内,感染WT,dam突变体或flhC突变体沙门氏菌的小鼠的单个动物的全身组织中的宿主基因表达取决于Peyer斑中的细菌载量。而且,在淋巴集结中的细菌负荷阈值对于刺激肝和脾中宿主基因的诱导是必要的。综上所述,这些结果表明,与在野生型和野生型沙门氏菌中观察到的免疫反应和疾病表现相比,细菌负荷和随之而来的菌株特异性细胞因子特征是在水坝突变沙门氏菌感染动物中观察到的宿主固有免疫反应和相关疾病表现的重要决定因素。 flhC突变沙门氏菌感染的动物。

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