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小鼠实验性金黄色葡萄球菌关节炎

Experimental Staphylococcus aureus arthritis in mice.

作者信息

Bremell T, Lange S, Yacoub A, Rydén C, Tarkowski A

机构信息

Department of Rheumatology and Clinical Bacteriology, University of Göteborg, Sweden.

出版信息

Infect Immun. 1991 Aug;59(8):2615-23. doi: 10.1128/iai.59.8.2615-2623.1991.

Abstract

Staphylococcus aureus arthritis is usually caused by bacteremia and is highly destructive. Controlled studies on septic arthritis in humans are difficult to perform, because the time of onset of the infection is unknown. Animal models of bacterial arthritis make it possible to control important variables in experimental studies. We present a mouse model of S. aureus arthritis in which the intravenous administration of 10(7) cells of S. aureus LS-1 induced arthritis or osteitis or both within 3 weeks in 80 to 90% of the mice. Signs of arthritis emerged within the first few days after the injection. An interesting finding was that the S. aureus strain used in this study binds bone sialoprotein, a glycoprotein known to be specifically localized to bone tissue. This new model of S. aureus arthritis enables the study of the kinetics of joint destruction and the host-bacterium relationship as well as therapeutical approaches to septic arthritis and osteomyelitis.

摘要

金黄色葡萄球菌性关节炎通常由菌血症引起,具有高度破坏性。对人类脓毒性关节炎进行对照研究很困难,因为感染的发病时间未知。细菌性关节炎的动物模型使在实验研究中控制重要变量成为可能。我们展示了一种金黄色葡萄球菌性关节炎小鼠模型,静脉注射10⁷个金黄色葡萄球菌LS-1细胞后,80%至90%的小鼠在3周内出现关节炎或骨炎或两者皆有。注射后几天内就出现了关节炎症状。一个有趣的发现是,本研究中使用的金黄色葡萄球菌菌株能结合骨唾液蛋白,这是一种已知特异性定位于骨组织的糖蛋白。这种新的金黄色葡萄球菌性关节炎模型能够研究关节破坏的动力学、宿主与细菌的关系以及脓毒性关节炎和骨髓炎的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/378b/258064/cda210181311/iai00044-0113-a.jpg

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