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The rovA mutant of Yersinia enterocolitica displays differential degrees of virulence depending on the route of infection.小肠结肠炎耶尔森菌的rovA突变体根据感染途径表现出不同程度的毒力。
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Yersinia enterocolitica evasion of the host innate immune response by V antigen-induced IL-10 production of macrophages is abrogated in IL-10-deficient mice.小肠结肠炎耶尔森菌通过V抗原诱导巨噬细胞产生白细胞介素-10来逃避宿主天然免疫反应的机制,在白细胞介素-10缺陷型小鼠中被消除。
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Qa-2-dependent selection of CD8alpha/alpha T cell receptor alpha/beta(+) cells in murine intestinal intraepithelial lymphocytes.鼠肠道上皮内淋巴细胞中Qa-2依赖性的CD8α/α T细胞受体α/β(+)细胞选择
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7
Interferon consensus sequence binding protein confers resistance against Yersinia enterocolitica.干扰素共有序列结合蛋白赋予对小肠结肠炎耶尔森菌的抗性。
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8
Construction of urease-negative mutants of Yersinia enterocolitica serotypes O:3 and o:8: role of urease in virulence and arthritogenicity.小肠结肠炎耶尔森菌O:3和O:8血清型脲酶阴性突变体的构建:脲酶在毒力和致关节炎性中的作用
Infect Immun. 2000 Feb;68(2):942-7. doi: 10.1128/IAI.68.2.942-947.2000.
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Ambiguous role of interleukin-12 in Yersinia enterocolitica infection in susceptible and resistant mouse strains.白细胞介素-12在易感和抗性小鼠品系小肠结肠炎耶尔森菌感染中的作用不明确。
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IL-18 (IFN-gamma-inducing factor) regulates early cytokine production in, and promotes resolution of, bacterial infection in mice.白细胞介素-18(干扰素-γ诱导因子)可调节小鼠细菌感染早期细胞因子的产生,并促进感染的消退。
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三种不同近交系小鼠口腔小肠结肠炎耶尔森菌感染的特征分析

Characterization of oral Yersinia enterocolitica infection in three different strains of inbred mice.

作者信息

Handley Scott A, Dube Peter H, Revell Paula A, Miller Virginia L

机构信息

Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

Infect Immun. 2004 Mar;72(3):1645-56. doi: 10.1128/IAI.72.3.1645-1656.2004.

DOI:10.1128/IAI.72.3.1645-1656.2004
PMID:14977972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC355989/
Abstract

Several studies have highlighted differences in the resistances of various mouse strains to intravenous (i.v.) infection with Yersinia enterocolitica. In particular, differences in resistance and immunological response between BALB/c and C57BL/6 mouse strains have been determined. Following i.v infection, C57BL/6 mice are more resistant to Y. enterocolitica than are BALB/c mice. However, because Y. enterocolitica is typically a food-borne pathogen, the oral route of infection more accurately reflects the natural route of infection. Therefore, it was of interest to ascertain if the differences in resistance between mouse strains observed for an i.v. infection can be recapitulated following an oral infection. C57BL/6j, BALB/cj, and 129X1/Svj mouse strains presented no differences in 50% lethal dose (LD(50)) following oral infection with Y. enterocolitica. Subsequent analysis of cytokine levels, bacterial colonization and immune cell populations following oral infection confirmed characteristics previously described following i.v. Y. enterocolitica infection. All tissues analyzed from each mouse strain demonstrated a polarized Th1 cytokine profile and inflammatory cell influx throughout a 7-day course of infection. This immune response was present in all tissues and increased as bacterial colonization progressed. The lack of a differing LD(50) phenotype and common trends in immunological response among the three mouse strains tested suggests that oral infection is a useful model for studying the host response to Y. enterocolitica infection.

摘要

多项研究强调了不同小鼠品系对小肠结肠炎耶尔森菌静脉内(i.v.)感染的抵抗力差异。特别是,已经确定了BALB/c和C57BL/6小鼠品系在抵抗力和免疫反应方面的差异。静脉内感染后,C57BL/6小鼠比BALB/c小鼠对小肠结肠炎耶尔森菌更具抵抗力。然而,由于小肠结肠炎耶尔森菌通常是一种食源性病原体,口服感染途径更准确地反映了自然感染途径。因此,确定在静脉内感染中观察到的小鼠品系之间的抵抗力差异在口服感染后是否可以重现是很有意义的。C57BL/6j、BALB/cj和129X1/Svj小鼠品系在口服小肠结肠炎耶尔森菌感染后的50%致死剂量(LD(50))方面没有差异。口服感染后对细胞因子水平、细菌定植和免疫细胞群体的后续分析证实了先前在静脉内小肠结肠炎耶尔森菌感染后描述的特征。在感染的7天过程中,从每个小鼠品系分析的所有组织都表现出极化的Th1细胞因子谱和炎症细胞流入。这种免疫反应在所有组织中都存在,并随着细菌定植的进展而增加。在所测试的三种小鼠品系中缺乏不同的LD(50)表型和免疫反应的共同趋势表明,口服感染是研究宿主对小肠结肠炎耶尔森菌感染反应的有用模型。