Massidda O, Montanari M P, Mingoia M, Varaldo P E
Institute of Microbiology, University of Ancona Medical School, Italy.
Antimicrob Agents Chemother. 1996 Dec;40(12):2769-74. doi: 10.1128/AAC.40.12.2769.
Ten epidemiologically unrelated Staphylococcus aureus isolates with borderline levels of susceptibility to antistaphylococcal penicillinase-resistant penicillins (PRPs) were investigated together with appropriate S. aureus control strains. By a nitrocefin microplate assay, all borderline PRP-susceptible test strains were found to produce comparable amounts of beta-lactamase. Hydrolytic activity against another chromogenic substrate (PADAC) and against the PRPs was also demonstrated in membrane preparations from induced cells of 9 of the 10 borderline test strains. When bacterial membranes were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, two methicillin-inducible bands of about 32 and 31 kDa were detected, after Coomassie blue staining, in the membrane protein patterns of the same nine borderline test strains. By gel renaturation and zymographic detection of beta-lactamase activity, both methicillin-inducible membrane proteins were detected with nitrocefin as a substrate, whereas only one band (presumably the smaller protein) was detected with PADAC. With the remaining borderline test strain (a40), only the larger band was detected in the renatured gels with nitrocefin as a substrate. Plasmid DNA analysis revealed that the borderline susceptible test strains, again with the exception of a40, shared a 17.2-kb plasmid yielding four HindIII fragments of 7.0, 5.3, 3.5, and 1.4 kb. In Western blot (immunoblot) experiments using rabbit antiserum to penicillin-binding protein (PBP) 2a, test strain a40, which did not share a number of features characteristically associated with the other borderline test strains, was eventually shown to produce PBP 2a. Five other S. aureus strains, belonging to phage group 94/96, were found to display the borderline phenotype, including such distinguishing features as the membrane-associated PRP- and PADAC-hydrolyzing activity, the two methicillin-inducible membrane proteins, and the 17.2-kb plasmid. These results suggest that borderline susceptible S. aureus strains share more common features than reduced susceptibility to PRPs.
对10株对抗葡萄球菌青霉素酶耐药青霉素(PRPs)敏感性处于临界水平且在流行病学上无关联的金黄色葡萄球菌分离株以及合适的金黄色葡萄球菌对照菌株进行了研究。通过头孢硝噻吩微孔板试验,发现所有临界PRP敏感试验菌株产生的β-内酰胺酶量相当。在10株临界试验菌株中的9株诱导细胞的膜制剂中,也证实了对另一种显色底物(PADAC)和对PRPs的水解活性。当通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析细菌膜时,在相同的9株临界试验菌株的膜蛋白图谱中,考马斯亮蓝染色后检测到两条约32 kDa和31 kDa的甲氧西林诱导条带。通过凝胶复性和β-内酰胺酶活性的酶谱检测,以头孢硝噻吩为底物检测到两种甲氧西林诱导的膜蛋白,而以PADAC为底物仅检测到一条带(可能是较小的蛋白)。对于其余的临界试验菌株(a40),以头孢硝噻吩为底物在复性凝胶中仅检测到较大的条带。质粒DNA分析表明,临界敏感试验菌株,除a40外,再次共享一个17.2 kb的质粒,产生7.0、5.3、3.5和1.4 kb的四个HindIII片段。在使用兔抗青霉素结合蛋白(PBP)2a血清的蛋白质印迹(免疫印迹)实验中,最终显示不具有许多与其他临界试验菌株特征相关特征的试验菌株a40产生PBP 2a。发现另外5株属于噬菌体组94/96的金黄色葡萄球菌菌株表现出临界表型,包括膜相关的PRP和PADAC水解活性、两种甲氧西林诱导的膜蛋白以及17.2 kb的质粒等特征。这些结果表明,临界敏感金黄色葡萄球菌菌株共享的共同特征比仅对PRPs敏感性降低更多。