Tesch W, Strässle A, Berger-Bächi B, O'Hara D, Reynolds P, Kayser F H
Institute of Medical Microbiology, University of Zürich, Switzerland.
Antimicrob Agents Chemother. 1988 Oct;32(10):1494-9. doi: 10.1128/AAC.32.10.1494.
A 6.2-kilobase chromosomal DNA fragment from a methicillin-resistant Staphylococcus epidermidis strain was cloned into Staphylococcus carnosus by using staphylococcal plasmid pCA44 as the vector. The recombinant plasmid obtained, pBBB21, conferred methicillin resistance on its host and was responsible for the synthesis of a low-affinity penicillin-binding protein (PBP), PBP 2'. PBP 2' determined by the S. epidermidis DNA and expressed as a membrane-bound PBP in S. carnosus reacted with monoclonal antibodies directed against PBP 2' of Staphylococcus aureus origin, and the cloned S. epidermidis DNA hybridized to the methicillin (mec)-specific DNA from S. aureus. These findings point to a common origin of the methicillin resistance determinant in staphylococci.
利用葡萄球菌质粒pCA44作为载体,将一株耐甲氧西林表皮葡萄球菌的6.2千碱基染色体DNA片段克隆到肉葡萄球菌中。所获得的重组质粒pBBB21赋予其宿主耐甲氧西林特性,并负责合成一种低亲和力青霉素结合蛋白(PBP),即PBP 2'。由表皮葡萄球菌DNA所决定并在肉葡萄球菌中作为膜结合PBP表达的PBP 2',与针对金黄色葡萄球菌来源的PBP 2'的单克隆抗体发生反应,并且克隆的表皮葡萄球菌DNA与来自金黄色葡萄球菌的甲氧西林(mec)特异性DNA杂交。这些发现表明葡萄球菌中甲氧西林耐药决定因素有共同的起源。