Gilbart J, Perry C R, Slocombe B
SmithKline Beecham Pharmaceuticals, Betchworth, Surrey, United Kingdom.
Antimicrob Agents Chemother. 1993 Jan;37(1):32-8. doi: 10.1128/AAC.37.1.32.
Mupirocin resistance in Staphylococcus aureus results from changes in the target enzyme, isoleucyl-tRNA synthetase (IRS). Twelve strains of S. aureus comprising four susceptible (MICs < or = 4 micrograms/ml), four intermediate level-resistant (MICs between 8 and 256 micrograms/ml), and four highly resistant (MICs > or = 512 micrograms/ml) isolates were examined for their IRS content and the presence of a gene known to encode high-level mupirocin resistance. Ion-exchange chromatography of cell extracts showed a single IRS active peak in mupirocin-susceptible strains, with 50% inhibitory concentrations (IC50s) of 0.7 to 3.0 ng of mupirocin per ml. In strains showing intermediate mupirocin resistance, similar single IRS activity peaks were observed, but these were less sensitive to inhibition, and the mupirocin IC50s for them were 19 to 43 ng/ml. Strains that were highly resistant to mupirocin displayed two distinct peaks; one was similar to that found with susceptible strains (IC50, 0.9 to 2.5 ng/ml), but an additional peak with an IC50 of 7,000 to 10,000 ng/ml was also observed. A strain cured of the plasmid encoding high-level mupirocin resistance lacked the resistant IRS peak. Restriction digests, produced by endonuclease NcoI, of total bacterial DNA isolated from the highly resistant strains hybridized with a mupirocin resistance gene probe, whereas DNA isolated from the intermediate level-resistant and susceptible strains did not. These results demonstrate that two different IRS enzymes were present in highly mupirocin-resistant S. aureus strains. In strains expressing intermediate levels of resistance, only a chromosomally encoded IRS which was inhibited less by mupirocin than IRS from fully susceptible strains was detected.
金黄色葡萄球菌对莫匹罗星的耐药性源于靶酶异亮氨酰 - tRNA合成酶(IRS)的变化。对12株金黄色葡萄球菌进行了研究,其中包括4株敏感菌株(最低抑菌浓度[MIC]≤4微克/毫升)、4株中度耐药菌株(MIC在8至256微克/毫升之间)和4株高度耐药菌株(MIC≥512微克/毫升),检测它们的IRS含量以及是否存在已知编码高水平莫匹罗星耐药性的基因。细胞提取物的离子交换色谱显示,莫匹罗星敏感菌株中有一个单一的IRS活性峰,莫匹罗星的50%抑制浓度(IC50)为每毫升0.7至3.0纳克。在表现出中度莫匹罗星耐药性的菌株中,观察到类似的单一IRS活性峰,但这些峰对抑制的敏感性较低,它们的莫匹罗星IC50为19至43纳克/毫升。对莫匹罗星高度耐药的菌株显示出两个不同的峰;一个与敏感菌株中的峰相似(IC50,0.9至2.5纳克/毫升),但还观察到一个IC50为7000至10000纳克/毫升的额外峰。一株治愈了编码高水平莫匹罗星耐药性质粒的菌株缺乏耐药性IRS峰。从高度耐药菌株中分离的总细菌DNA经核酸内切酶NcoI酶切后,与莫匹罗星耐药基因探针杂交,而从中度耐药和敏感菌株中分离的DNA则未杂交。这些结果表明,高度莫匹罗星耐药的金黄色葡萄球菌菌株中存在两种不同的IRS酶。在表达中度耐药水平的菌株中,仅检测到一种染色体编码的IRS,与完全敏感菌株的IRS相比,它受莫匹罗星的抑制作用较小。