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体外延迟抗生素诱导的大肠杆菌裂解与脂多糖释放增加相关。

Delayed antibiotic-induced lysis of Escherichia coli in vitro is correlated with enhancement of LPS release.

作者信息

Van Den Berg C, de Neeling A J, Schot C S, Hustinx W N, Wemer J, de Wildt D J

机构信息

Laboratory for Medicines and Medical Devices, National Institute of Public Health and Environmental Protection, Bilthoven, The Netherlands.

出版信息

Scand J Infect Dis. 1992;24(5):619-27. doi: 10.3109/00365549209054648.

Abstract

A kinetic turbidimetric Limulus amebocyte lysate (LAL) assay was used to study the effects of gentamicin, amoxycillin and ciprofloxacin (16 x MIC) upon release of lipopolysaccharide at different stages of a growing Escherichia coli 055:B5:H culture in vitro. In this model a linear correlation was present between the logarithms of colony counts and free LAL activities. Untreated E. coli grew from log values of 4.9 +/- 0.15 (low inoculum) and 6.8 +/- 0.08 cfu/ml (high inoculum) at t = 0 to 8.9 +/- 0.05 and 9.1 +/- 0.13 cfu/ml at t = 6 h, respectively. The log values of basal free LAL activities at low and high inoculum sizes were 1.9 +/- 0.07 and 3.3 +/- 0.14 endotoxin units/ml, increasing 2100- and 69-fold, respectively during a 6-h growth. Amoxycillin-induced lysis was not significantly associated with an increase in free LAL activity. Efficacy of bacterial killing by gentamicin was high, but free LAL activity increased only 3.2- and 7.7-fold at the low and high inoculum experiments, respectively. Ciprofloxacin induced cell filamentation during the experiments. At low and high inoculum conditions exposure to ciprofloxacin induced a 43- and 68-fold increase in free LAL activities, respectively. Our data indicate that (a) LPS is released as long as E. coli remain structurally intact; (b) LPS release is enhanced when bacterial biomass increases; and (c) are taken as evidence against the concept of lysis-correlated LPS release.

摘要

采用动态比浊法鲎试剂检测,研究庆大霉素、阿莫西林和环丙沙星(16倍最低抑菌浓度)对体外培养的大肠杆菌055:B5:H不同生长阶段脂多糖释放的影响。在该模型中,菌落计数的对数与游离鲎试剂活性之间呈线性相关。未处理的大肠杆菌在t = 0时,低接种量时对数数值为4.9±0.15 cfu/ml,高接种量时为6.8±0.08 cfu/ml,在t = 6 h时分别增长至8.9±0.05和9.1±0.13 cfu/ml。低接种量和高接种量时基础游离鲎试剂活性的对数数值分别为1.9±0.07和3.3±0.14内毒素单位/ml,在6小时的生长过程中分别增加了2100倍和69倍。阿莫西林诱导的裂解与游离鲎试剂活性的增加无显著相关性。庆大霉素杀菌效果良好,但在低接种量和高接种量实验中,游离鲎试剂活性仅分别增加了3.2倍和7.7倍。环丙沙星在实验过程中诱导细胞丝状化。在低接种量和高接种量条件下,暴露于环丙沙星分别使游离鲎试剂活性增加了43倍和68倍。我们的数据表明:(a)只要大肠杆菌结构保持完整,脂多糖就会释放;(b)细菌生物量增加时,脂多糖释放会增强;(c)这些数据作为反对脂多糖释放与裂解相关概念的证据。

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