Richards R M, Eumkeb G, Marshall D
School of Pharmacy, Robert Gordon University, Aberdeen, Scotland, Great Britain.
Microbios. 1997;92(372-373):183-97.
The test organism was Escherichia coli 1810 which was highly resistant to trimethoprim (TMP). Electron microscopy (EM) of cells grown in the presence of subinhibitory concentrations of 300 micrograms/ml sulphadiazine (SD) and/or 300 micrograms/ml TMP indicated marked structural damage. No effect on the outer membrane (OM) or ultrastructure of E. coli 1810 was observed with 7.68 micrograms/ml TMP and/or 16.9 micrograms/ml SD. Concentrations of antibacterials affecting the ultrastructure of the bacterial cells of resistant and sensitive E. coli as determined by EM, were shown by a permeability probe (Triton X-100) to alter the OM permeability and to partially inhibit growth of E. coli 1810 cultures. It was concluded that, since the action of SD and TMP, singly and in combination, on the cell structure of E. coli 1810 took place only at concentrations approaching the respective MICs, then this was a part of their normal mechanisms of antibacterial action.
测试菌株为对甲氧苄啶(TMP)高度耐药的大肠杆菌1810。对在亚抑制浓度300微克/毫升磺胺嘧啶(SD)和/或300微克/毫升TMP存在下生长的细胞进行电子显微镜(EM)观察,结果显示存在明显的结构损伤。7.68微克/毫升TMP和/或16.9微克/毫升SD对大肠杆菌1810的外膜(OM)或超微结构没有影响。通过电子显微镜确定的影响耐药和敏感大肠杆菌细菌细胞超微结构的抗菌剂浓度,经通透性探针(曲拉通X-100)显示会改变OM通透性并部分抑制大肠杆菌1810培养物的生长。得出的结论是,由于SD和TMP单独及联合作用于大肠杆菌1810的细胞结构仅在接近各自最低抑菌浓度(MIC)的浓度下发生,因此这是它们正常抗菌作用机制的一部分。