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XF-73,一种具有快速杀菌活性的新型抗葡萄球菌膜活性剂。

XF-73, a novel antistaphylococcal membrane-active agent with rapid bactericidal activity.

作者信息

Ooi Nicola, Miller Keith, Hobbs Joanne, Rhys-Williams William, Love William, Chopra Ian

机构信息

Antimicrobial Research Centre and Institute of Molecular and Cellular Biology, University of Leeds, Leeds, UK.

出版信息

J Antimicrob Chemother. 2009 Oct;64(4):735-40. doi: 10.1093/jac/dkp299. Epub 2009 Aug 18.

Abstract

OBJECTIVES

XF-73 is a novel porphyrin antibacterial agent previously reported to inhibit a range of gram-positive bacterial species, including Staphylococcus aureus. Its mode of action is unknown. Using S. aureus as a model organism we sought to examine the basis of its antibacterial activity.

METHODS

The effects of XF-73 on the growth and survival of S. aureus SH1000 were investigated by viable count and culture absorbance techniques. Inhibition of macromolecular synthesis and disruption of membrane integrity after exposure to XF-73 were examined by radiolabelling experiments, the BacLight fluorescent dye assay and measurement of K(+) and ATP leakage from the cell. The effect of XF-73 on a staphylococcal coupled transcription-translation system was also investigated.

RESULTS

XF-73 was rapidly bactericidal against S. aureus SH1000 and demonstrated more rapid killing kinetics than all other comparator agents when tested at an equivalent multiple (4x) of the MIC. Exposure of S. aureus to XF-73 for 10 min completely inhibited DNA, RNA and protein synthesis. XF-73 had no effect on transcription and translation in vitro. Cells exposed to XF-73 gave a positive response in the BacLight assay, which detects membrane damage. The drug also caused substantial loss of K(+) and ATP from the cell, but did not promote bacterial lysis.

CONCLUSIONS

XF-73 exhibited rapid membrane-perturbing activity, which is likely to be responsible for inhibition of macromolecular synthesis and the death of staphylococci exposed to the drug.

摘要

目的

XF - 73是一种新型卟啉类抗菌剂,此前报道其可抑制包括金黄色葡萄球菌在内的多种革兰氏阳性菌。其作用机制尚不清楚。我们以金黄色葡萄球菌作为模式生物,试图探究其抗菌活性的基础。

方法

通过活菌计数和培养物吸光度技术研究XF - 73对金黄色葡萄球菌SH1000生长和存活的影响。通过放射性标记实验、BacLight荧光染料测定以及测量细胞内钾离子(K⁺)和三磷酸腺苷(ATP)泄漏情况,检测暴露于XF - 73后大分子合成的抑制和膜完整性的破坏。还研究了XF - 73对葡萄球菌偶联转录 - 翻译系统的影响。

结果

XF - 73对金黄色葡萄球菌SH1000具有快速杀菌作用,在以最低抑菌浓度(MIC)的等效倍数(4倍)进行测试时,其杀菌动力学比所有其他对照剂都更快。将金黄色葡萄球菌暴露于XF - 73 10分钟可完全抑制DNA、RNA和蛋白质合成。XF - 73在体外对转录和翻译没有影响。暴露于XF - 73的细胞在检测膜损伤的BacLight测定中呈阳性反应。该药物还导致细胞内大量钾离子和ATP流失,但未促进细菌裂解。

结论

XF - 73表现出快速的膜扰动活性,这可能是抑制大分子合成以及导致暴露于该药物的葡萄球菌死亡的原因。

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