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头孢菌素的杀菌和溶菌活性与大肠杆菌培养物细胞体积变化之间的关系

Relationship between the bactericidal and bacteriolytic activity of cephalosporins and changes in the cell volumes of Escherichia coli cultures.

作者信息

Schulz E, von Klitzing L, Marre R, Sack K

出版信息

Infection. 1985 Sep-Oct;13(5):235-9. doi: 10.1007/BF01667219.

Abstract

The bactericidal effect of cefoxitin and cefotaxime in relation to concentration and exposure time, as demonstrated by the killing curve diagrams of Escherichia coli cultures, was compared with the degree of bacteriolysis and the cell volume increase measured by the coulter counter-channel analyser system. Human plasma ultrafiltrate was used as the growth medium. Cefoxitin has a higher bactericidal activity than cefotaxime. With increasing concentrations the bactericidal efficacy of cefoxitin increases more rapidly in the lower range of concentrations (2-10 mg/l) than in the higher range (10-40 mg/l). In contrast, the bactericidal effect of cefotaxime in the range 0.06-1.2 mg/l is virtually constant and can only be increased by high levels (10-40 mg/l). The morphometric effect of cefoxitin on E. coli cultures, as demonstrated by volume distribution curves, is characterized by intensive and rapidly appearing bacteriolysis 20 min after exposure to the antibiotic without a preceding increase in bacterial cell volume. Higher concentrations result in an earlier onset of bacteriolysis. In contrast, the application of cefotaxime reveals a massive increase in bacterial cell volume (more than five-fold) with a delayed (greater than 2 h) onset of bacteriolysis. High cefotaxime concentrations reduce the extent of bacterial cell volume increase, associated with an earlier and more intensive onset of bacteriolysis. With both cephalosporins, the bacterial cell alterations are particularly dependent on the exposure time. There is evidently a close correlation between bactericidal and bacteriolytic activity. This is valid both for the two cephalosporins and generally for the concentration-activity relationships.

摘要

通过大肠杆菌培养物的杀菌曲线图所示,将头孢西丁和头孢噻肟的杀菌效果与浓度和暴露时间的关系,与通过库尔特计数器通道分析仪系统测量的细菌溶解程度和细胞体积增加程度进行了比较。使用人血浆超滤液作为生长培养基。头孢西丁比头孢噻肟具有更高的杀菌活性。随着浓度的增加,头孢西丁在较低浓度范围(2-10mg/L)内的杀菌效力比在较高浓度范围(10-40mg/L)内增加得更快。相比之下,头孢噻肟在0.06-1.2mg/L范围内的杀菌效果几乎恒定,只有在高浓度(10-40mg/L)时才能增强。如体积分布曲线所示,头孢西丁对大肠杆菌培养物的形态计量学作用的特征是,在接触抗生素20分钟后出现强烈且迅速的细菌溶解,而细菌细胞体积在此之前没有增加。较高浓度会导致细菌溶解更早开始。相比之下,应用头孢噻肟会使细菌细胞体积大幅增加(超过五倍),细菌溶解延迟(超过2小时)开始。高浓度的头孢噻肟会降低细菌细胞体积增加的程度,同时使细菌溶解更早且更强烈地开始。对于这两种头孢菌素,细菌细胞的改变特别依赖于暴露时间。杀菌活性和细菌溶解活性之间显然存在密切相关性。这对于这两种头孢菌素以及一般的浓度-活性关系都是成立的。

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