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头孢菌素与耐甲氧西林金黄色葡萄球菌青霉素结合蛋白的相互作用。

Interaction of cephalosporins with penicillin-binding proteins of methicillin-resistant Staphylococcus aureus.

作者信息

Truesdell S E, Zurenko G E, Laborde A L

机构信息

Research Laboratories, Upjohn Company, Kalamazoo, MI 49001.

出版信息

J Antimicrob Chemother. 1989 Apr;23 Suppl D:13-9. doi: 10.1093/jac/23.suppl_d.13.

Abstract

The binding affinity of cefmetazole for penicillin binding proteins (PBPs) of methicillin resistant Staphylococcus aureus (MRSA) was compared with the affinities of cefazolin, cefotetan, and cefoxitin for these same sites. Overall, cefmetazole was found to have comparable or higher affinity for PBP1, PBP2, and PBP3 than cefoxitin or cefotetan; its affinity for these PBPs is lower than that of cefazolin. Interestingly, the antibiotic showed a somewhat greater affinity for PBP2' (PBP2a) than cefazolin, cefotetan, and cefoxitin. These results suggest that the somewhat lower MICs detected with cefmetazole for MRSA may be a consequence of the interaction of the antibiotic with PBP2'.

摘要

将头孢美唑对耐甲氧西林金黄色葡萄球菌(MRSA)青霉素结合蛋白(PBPs)的结合亲和力与头孢唑林、头孢替坦和头孢西丁对相同位点的亲和力进行了比较。总体而言,发现头孢美唑对PBP1、PBP2和PBP3的亲和力与头孢西丁或头孢替坦相当或更高;其对这些PBPs的亲和力低于头孢唑林。有趣的是,该抗生素对PBP2'(PBP2a)的亲和力比头孢唑林、头孢替坦和头孢西丁略高。这些结果表明,头孢美唑对MRSA检测到的MIC略低可能是该抗生素与PBP2'相互作用的结果。

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