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头孢菌素对大肠杆菌的杀菌活性及细胞体积变化诱导作用

Bactericidal activity and induction of cell volume alterations of cephalosporins in Escherichia coli.

作者信息

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

出版信息

Chemotherapy. 1985;31(6):425-32. doi: 10.1159/000238370.

DOI:10.1159/000238370
PMID:3908008
Abstract

The bactericidal efficacy of cefuroxime and cephacetril on Escherichia coli cultures was measured by killing curves. Simultaneously bacterial cell volumes were analysed by electronic particle counting using a Coulter Counter Channelanalyser system in order to study the relationship between bactericidal activity and bacterial cell volume alterations. Various concentrations (2-120 mg/l cefuroxime and 16-120 mg/l cephacetril) and different exposure times (over a time period of 12 h) were used. Growth medium was human plasma ultrafiltrate. The bactericidal activity of cefuroxime, as measured by the rate of killing of the E. coli culture, was independent of the concentration and constant in the range 4-120 mg/l. The characteristic cefuroxime-induced change in bacterial cell volume was a marked volume increase up to a maximum of 5-fold after 160-200 min exposure with a low-grade bacteriolysis following. The cefuroxime-induced bacterial volume changes were, in accordance with the bactericidal testing, almost independent of the concentration. In contrast, the killing curves for cephacetril strongly depended on the drug concentration. However, this effect was short-lived and regrowth of the E. coli culture followed. The typical cephacetril-induced volume distribution curves were also highly concentration-dependent. With increasing drug levels bacterial cell volume increased up to 20-fold, and regrowth of a persisting bacterial population occurred at lower antibiotic concentrations. Bacteriolysis started earlier than with cefuroxime. The relationship between loss of viability and cell volume increase was more marked with cefuroxime than with cephacetril.

摘要

通过杀菌曲线测定头孢呋辛和头孢乙腈对大肠杆菌培养物的杀菌效果。同时,使用库尔特计数器通道分析仪系统通过电子粒子计数分析细菌细胞体积,以研究杀菌活性与细菌细胞体积变化之间的关系。使用了各种浓度(2 - 120 mg/l头孢呋辛和16 - 120 mg/l头孢乙腈)和不同暴露时间(在12小时的时间段内)。生长培养基为人血浆超滤物。以大肠杆菌培养物的杀灭率衡量,头孢呋辛的杀菌活性与浓度无关,在4 - 120 mg/l范围内保持恒定。头孢呋辛诱导的细菌细胞体积特征性变化是在暴露160 - 200分钟后体积显著增加,最大可达5倍,随后伴有轻度细菌溶解。与杀菌试验一致,头孢呋辛诱导的细菌体积变化几乎与浓度无关。相比之下,头孢乙腈的杀菌曲线强烈依赖于药物浓度。然而,这种作用是短暂的,随后大肠杆菌培养物会重新生长。典型的头孢乙腈诱导的体积分布曲线也高度依赖于浓度。随着药物水平的增加,细菌细胞体积增加高达20倍,并且在较低抗生素浓度下会出现持续细菌群体的重新生长。细菌溶解比头孢呋辛更早开始。头孢呋辛导致的活力丧失与细胞体积增加之间的关系比头孢乙腈更为明显。

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1
Bactericidal activity and induction of cell volume alterations of cephalosporins in Escherichia coli.头孢菌素对大肠杆菌的杀菌活性及细胞体积变化诱导作用
Chemotherapy. 1985;31(6):425-32. doi: 10.1159/000238370.
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Relationship between the bactericidal and bacteriolytic activity of cephalosporins and changes in the cell volumes of Escherichia coli cultures.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
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