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亚抑菌浓度抗生素对金黄色葡萄球菌与纤连蛋白相互作用的影响。

Effects of subinhibitory concentrations of antibiotics on Staphylococcus aureus interactions with fibronectin.

作者信息

Proctor R A, Hamill R J, Mosher D F, Textor J A, Olbrantz P J

出版信息

J Antimicrob Chemother. 1983 Oct;12 Suppl C:85-95. doi: 10.1093/jac/12.suppl_c.85.

Abstract

Bacterial adherence to host tissues relies on interactions between tissue macromolecules and bacterial surface molecules. One of the major predisposing factors to infection with Staphylococcus aureus is trauma to tissues. A common element in traumatized tissues is fibronectin. In previous studies, we have shown that fibronectin binds to Staph. aureus. In this paper, we have investigated the effects of subinhibitory concentrations of antibiotics on fibronectin interactions with Staph. aureus. Exposure of Staph. aureus to 1/4 MIC of penicillin increases the number of binding sites and enhances adherence of Staph. aureus to a collagen-fibronectin matrix. Chloramphenicol, erythromycin, clindamycin, and U57,930E all decreased the number of binding sites. Also, U57,930E reduced Staph. aureus adherence to a collagen-fibronectin matrix. Taken together, these data suggest that penicillin may enhance Staph. aureus adherence to tissue fibronectin whereas U57,930E might reduce such binding.

摘要

细菌对宿主组织的黏附依赖于组织大分子与细菌表面分子之间的相互作用。金黄色葡萄球菌感染的主要诱发因素之一是组织创伤。创伤组织中的一个常见成分是纤连蛋白。在先前的研究中,我们已经表明纤连蛋白能与金黄色葡萄球菌结合。在本文中,我们研究了亚抑菌浓度的抗生素对纤连蛋白与金黄色葡萄球菌相互作用的影响。将金黄色葡萄球菌暴露于1/4 MIC的青霉素中会增加结合位点的数量,并增强金黄色葡萄球菌对胶原 - 纤连蛋白基质的黏附。氯霉素、红霉素、克林霉素和U57,930E均降低了结合位点的数量。此外,U57,930E降低了金黄色葡萄球菌对胶原 - 纤连蛋白基质的黏附。综上所述,这些数据表明青霉素可能增强金黄色葡萄球菌对组织纤连蛋白的黏附,而U57,930E可能会减少这种结合。

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