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鼠伤寒沙门氏菌毒力相关质粒的新型毒力特性:免疫抑制和脾肿大刺激。

Novel virulence properties of the Salmonella typhimurium virulence-associated plasmid: immune suppression and stimulation of splenomegaly.

作者信息

Hoertt B E, Ou J, Kopecko D J, Baron L S, Warren R L

机构信息

Department of Microbiology and Immunology, School of Medicine, College of Science and Mathematics, Wright State University, Dayton, Ohio 45431.

出版信息

Plasmid. 1989 Jan;21(1):48-58. doi: 10.1016/0147-619x(89)90086-3.

Abstract

Mice infected subcutaneously with wild-type Salmonella typhimurium, SR11, developed a significant splenomegaly when compared with mice infected with an equal number of a plasmid-cured strain. Further, the bacterial load in the spleen at 14 days after infection, measured as colony-forming units per gram tissue, was significantly higher in mice infected with the parent strain than in mice infected with the plasmid-cured strain. These data confirm the previously reported plasmid-associated ability of Salmonella to multiply within the spleen. In addition, lymph node cells (LNC) from mice infected with the parent strain had a significantly reduced ability to proliferate in response to concanavalin A, a T-cell mitogen, and to heat-killed S. typhimurium cells when compared with LNC isolated from mice infected with the plasmid-cured strain. Finally, reintroduction of a functional Tn5-tagged 90-kb plasmid into a plasmid-free strain restored its capacity to cause a marked splenomegaly and to suppress lymph node cell proliferation in BALB/c mice. These data demonstrate that the 90-kb plasmid of highly virulent S. typhimurium strains mediates several novel pathogenic properties in infected mice: (1) enhancement of the ability of Salmonella to multiply within the spleen; (2) stimulation of a splenic inflammatory response as displayed by marked splenomegaly; and (3) a general suppression of lymphocyte responsiveness to both T-cell mitogens and specific Salmonella antigens.

摘要

与感染相同数量质粒消除菌株的小鼠相比,皮下感染野生型鼠伤寒沙门氏菌SR11的小鼠出现了明显的脾肿大。此外,以每克组织的菌落形成单位衡量,感染后14天脾脏中的细菌载量,感染亲本菌株的小鼠显著高于感染质粒消除菌株的小鼠。这些数据证实了先前报道的沙门氏菌与质粒相关的在脾脏内增殖的能力。此外,与从感染质粒消除菌株的小鼠中分离的淋巴结细胞(LNC)相比,感染亲本菌株的小鼠的LNC对T细胞有丝分裂原伴刀豆球蛋白A和热灭活的鼠伤寒沙门氏菌细胞反应的增殖能力显著降低。最后,将功能性Tn5标记的90 kb质粒重新导入无质粒菌株,恢复了其在BALB/c小鼠中引起明显脾肿大和抑制淋巴结细胞增殖的能力。这些数据表明,高毒力鼠伤寒沙门氏菌菌株的90 kb质粒在感染小鼠中介导了几种新的致病特性:(1)增强沙门氏菌在脾脏内增殖的能力;(2)通过明显的脾肿大表现出的脾脏炎症反应的刺激;(3)对T细胞有丝分裂原和特定沙门氏菌抗原的淋巴细胞反应性的普遍抑制。

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