Hiramatsu K, Suzuki E, Takayama H, Katayama Y, Yokota T
Department of Microbiology, Faculty of Medicine, Juntendo University, Tokyo, Japan.
Antimicrob Agents Chemother. 1990 Apr;34(4):600-4. doi: 10.1128/AAC.34.4.600.
The stability of methicillin resistance (Mcr) in three independent clinical isolates, MR108, MR6, and MR61, of methicillin-resistant Staphylococcus aureus (MRSA) was studied. The Mcr phenotype was stably maintained in the progeny of all three MRSA clones carrying penicillinase plasmids. However, when the clones were tested after elimination of the plasmids, methicillin-susceptible (Mcs) subclones appeared at various frequencies. Seven Mcs subclones were classified into two groups based on their stabilities. Five Mcs subclones, which were derived from homogeneous strains MR108 and MR61, were stably susceptible. They lost penicillin-binding protein 2' production, and moreover, the mecA gene was deleted in four of five subclones. Two subclones were derived from heterogeneous strain MR6. They were very unstable, and more than half of their progeny were Mcr revertants. However, the remainder were stably Mcs and had lost penicillin-binding protein 2' and the mecA gene. We propose that penicillinase plasmids, which are present in most MRSA strains, play an important role in the stability and phenotypic expression of the mecA gene.
对耐甲氧西林金黄色葡萄球菌(MRSA)的三个独立临床分离株MR108、MR6和MR61中耐甲氧西林(Mcr)的稳定性进行了研究。Mcr表型在所有携带青霉素酶质粒的三个MRSA克隆的子代中均稳定维持。然而,当在消除质粒后对这些克隆进行测试时,出现了不同频率的甲氧西林敏感(Mcs)亚克隆。根据其稳定性,七个Mcs亚克隆被分为两组。五个来自同源菌株MR108和MR61的Mcs亚克隆对甲氧西林稳定敏感。它们失去了青霉素结合蛋白2'的产生,此外,五个亚克隆中有四个的mecA基因被删除。两个亚克隆来自异源菌株MR6。它们非常不稳定,超过一半的子代是Mcr回复株。然而,其余的对甲氧西林稳定敏感,并且失去了青霉素结合蛋白2'和mecA基因。我们认为,大多数MRSA菌株中存在的青霉素酶质粒在mecA基因的稳定性和表型表达中起重要作用。