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环丙沙星亚抑菌浓度对偶然分枝杆菌突变率的影响。

Effect of subinhibitory concentrations of ciprofloxacin on Mycobacterium fortuitum mutation rates.

作者信息

Gillespie Stephen H, Basu Shreya, Dickens Anne L, O'Sullivan Denise M, McHugh Timothy D

机构信息

Centre for Medical Microbiology, University College London, Hampstead Campus, Rowland Hill St., London NW3 2PF, UK.

出版信息

J Antimicrob Chemother. 2005 Aug;56(2):344-8. doi: 10.1093/jac/dki191. Epub 2005 Jun 14.

Abstract

OBJECTIVES

Fluoroquinolones have found a place in the management of mycobacterial diseases including tuberculosis. It has been previously shown that subinhibitory concentrations of quinolones increase the mutation rate in Escherichia coli and staphylococci. The purpose of this study is to extend this observation to mycobacteria and to quantify mutation rates.

METHODS

The mutation rate in Mycobacterium fortuitum to ciprofloxacin, levofloxacin, moxifloxacin, rifampicin, erythromycin and gentamicin resistance was determined when grown with and without various sub-MIC concentrations of ciprofloxacin.

RESULTS

M. fortuitum exposed to 1/2 MIC ciprofloxacin had an increase in the mutation rate of between 72- and 120-fold when selected on quinolones or other antimycobacterial antibiotics. Smaller, but significant increases in mutation rate were seen when the organism was exposed to lower concentrations (1/4 MIC and 1/8 MIC).

CONCLUSIONS

These data show that sub-MIC concentrations of fluoroquinolone significantly increase mutation rates and these data suggest that care must be taken to ensure that bacteria are not exposed to subinhibitory concentrations when adding quinolones to a regimen used to treat mycobacterial infection.

摘要

目的

氟喹诺酮类药物在包括结核病在内的分枝杆菌疾病治疗中已占有一席之地。先前已有研究表明,喹诺酮类药物的亚抑菌浓度会增加大肠杆菌和葡萄球菌的突变率。本研究的目的是将这一观察结果扩展至分枝杆菌,并对突变率进行量化。

方法

在有和没有各种亚最低抑菌浓度(sub-MIC)的环丙沙星存在的情况下培养偶然分枝杆菌,测定其对环丙沙星、左氧氟沙星、莫西沙星、利福平、红霉素和庆大霉素耐药的突变率。

结果

当在喹诺酮类药物或其他抗分枝杆菌抗生素上进行选择时,暴露于1/2 MIC环丙沙星的偶然分枝杆菌的突变率增加了72至120倍。当该菌暴露于较低浓度(1/4 MIC和1/8 MIC)时,突变率也有较小但显著的增加。

结论

这些数据表明,氟喹诺酮类药物的亚MIC浓度会显著增加突变率,这些数据提示,在将喹诺酮类药物添加到用于治疗分枝杆菌感染的方案中时,必须注意确保细菌不暴露于亚抑菌浓度。

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