Handley Scott A, Dube Peter H, Revell Paula A, Miller Virginia L
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Infect Immun. 2004 Mar;72(3):1645-56. doi: 10.1128/IAI.72.3.1645-1656.2004.
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.
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。