Finan J E, Rosato A E, Dickinson T M, Ko D, Archer Gordon L
Department of Medicine, Medical College of Virginia, Virginia Commonwealth University, Richmond, Virginia 23298-0049, USA.
Antimicrob Agents Chemother. 2002 Jan;46(1):24-30. doi: 10.1128/AAC.46.1.24-30.2002.
Staphylococci that acquire the mecA gene are usually resistant to beta-lactam antibiotics (methicillin or oxacillin resistance). mecA encodes a penicillin-binding protein (PBP 2a) that has a reduced affinity for beta-lactams. In some isolates with methicillin or oxacillin resistance, only a small proportion (< or =0.1%) of the population expresses resistance to > or =10 microg of oxacillin per ml (heterotypic resistance [HeR]), while in other isolates most of the population expresses resistance (homotypic resistance [HoR]). In the present study, growth of Staphylococcus aureus or Staphylococcus epidermidis strains with HeR in concentrations of oxacillin (0.3 to 0.7 microg/ml) that produced a fall or a lag in optical density converted the strains from the HeR to the HoR phenotype. The conversion from the HeR to the HoR phenotype appeared to be due to the selection of a highly resistant mutant population, as determined by fluctuation analysis and the failure of populations with HoR to revert to HeR after 60 generations of growth in antibiotic-free media. The frequencies of conversion were as high as 10(-3) to 10(-2). Conversion to HoR required an intact mecA gene and an increase in the level of mecA transcription since no highly resistant subpopulation could be selected after growth in oxacillin when mecA transcription was constitutively repressed or when mecA had been inactivated. In addition, in both S. epidermidis and S. aureus the level of resistance to vancomycin, which also acts directly on the staphylococcal cell wall, was greater among convertants with HoR than their isogenic parents. The conversion of a population from HeR to HoR involves the selection of a mutation(s) that occurs at a high frequency and most likely requires abundant PBP 2a.
获得mecA基因的葡萄球菌通常对β-内酰胺类抗生素耐药(耐甲氧西林或耐苯唑西林)。mecA编码一种对β-内酰胺类亲和力降低的青霉素结合蛋白(PBP 2a)。在一些耐甲氧西林或耐苯唑西林的分离株中,只有一小部分群体(≤0.1%)对每毫升≥10微克苯唑西林表现出耐药性(异型耐药[HeR]),而在其他分离株中,大多数群体表现出耐药性(同型耐药[HoR])。在本研究中,金黄色葡萄球菌或表皮葡萄球菌HeR菌株在能使光密度下降或滞后的苯唑西林浓度(0.3至0.7微克/毫升)中生长,可使菌株从HeR表型转变为HoR表型。从HeR表型转变为HoR表型似乎是由于选择了高度耐药的突变群体,这通过波动分析以及HoR群体在无抗生素培养基中生长60代后未能恢复为HeR来确定。转变频率高达10⁻³至10⁻²。转变为HoR需要完整的mecA基因以及mecA转录水平的增加,因为当mecA转录被组成性抑制或mecA失活时,在苯唑西林中生长后无法选择出高度耐药的亚群体。此外,在表皮葡萄球菌和金黄色葡萄球菌中,对同样直接作用于葡萄球菌细胞壁的万古霉素的耐药水平,HoR转变株比其同基因亲本更高。群体从HeR转变为HoR涉及高频发生的一个或多个突变的选择,并且很可能需要大量的PBP 2a。