Elliott T S, Greenwood D
J Med Microbiol. 1983 Aug;16(3):351-62. doi: 10.1099/00222615-16-3-351.
The morphological response of Pseudomonas aeruginosa to azlocillin, ticarcillin and cefsulodin was investigated by electron microscopy. Each antibiotic initially caused the formation of filaments. On further incubation in the presence of azlocillin, deposits of dense intracellular material were observed; these were absent from cells exposed to the other two antibiotics. On continued incubation, lysis of the filaments occurred, but the mode of lysis differed between the antibiotics: azlocillin caused breakage at a restricted number of sites in the cell wall, ticarcillin produced breakage at many points and cefsulodin caused extensive cell-wall damage. In addition, ticarcillin and cefsulodin appeared to cause more lysis and spheroplast formation than did azlocillin. The morphological changes correlated with turbidimetric measurements of bacterial response to the three antibiotics, which showed ticarcillin and cefsulodin to act more rapidly than azlocillin.
通过电子显微镜研究了铜绿假单胞菌对阿洛西林、替卡西林和头孢磺啶的形态学反应。每种抗生素最初都会导致丝状结构的形成。在阿洛西林存在的情况下进一步孵育时,观察到细胞内有致密物质沉积;而暴露于其他两种抗生素的细胞中则没有这种情况。继续孵育时,丝状结构会发生裂解,但不同抗生素的裂解方式不同:阿洛西林导致细胞壁在有限数量的位点处断裂,替卡西林在许多点处产生断裂,头孢磺啶则导致广泛的细胞壁损伤。此外,与阿洛西林相比,替卡西林和头孢磺啶似乎会引起更多的裂解和原生质球形成。形态学变化与细菌对这三种抗生素反应的比浊法测量结果相关,结果显示替卡西林和头孢磺啶的作用比阿洛西林更快。