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评价四十种新的吩噻嗪衍生物对参考大肠杆菌、肠炎沙门氏菌、粪肠球菌和金黄色葡萄球菌菌株固有外排泵系统的活性。

Evaluation of forty new phenothiazine derivatives for activity against intrinsic efflux pump systems of reference Escherichia coli, Salmonella Enteritidis, Enterococcus faecalis and Staphylococcus aureus strains.

机构信息

Unit of Mycobacteriology, Institute of Hygiene and Tropical Medicine, Rua da Junqueira 96, 1349-008 Lisboa, Portugal.

出版信息

In Vivo. 2011 Sep-Oct;25(5):719-24.

Abstract

BACKGROUND

Because phenothiazines inhibit efflux pumps of bacteria, forty new phenothiazine derivatives were tested for their inhibition of the efflux pump systems of Gram-positive and Gram-negative pathogenic bacteria.

MATERIALS AND METHODS

Detection of efflux pump activity was conducted by a previously described automated fluorimetric method.

RESULTS

Although many of the compounds significantly inhibited efflux by distinct bacteria, four compounds had exceptional activity against the efflux pump systems of the pathogenic wild type bacteria Escherichia coli, Salmonella Enteritidis, Enterococcus faecalis and Staphylococcus aureus. These four compounds were then evaluated for ability to reduce or reverse resistance of multi-drug resistant members of Escherichia coli, Salmonella and Staphylococcus aureus whose MDR phenotypes are mediated by specific over-expressed efflux pumps. One of the compounds, 2173, significantly reduced resistance of MDR Staphylococcus aureus.

CONCLUSION

These results suggest possible use of compound 2173 for therapy of infections caused by this organism.

摘要

背景

由于吩噻嗪类抑制细菌的外排泵,因此测试了 40 种新型吩噻嗪衍生物对革兰氏阳性和革兰氏阴性致病菌的外排泵系统的抑制作用。

材料与方法

通过先前描述的自动荧光法检测外排泵活性。

结果

尽管许多化合物可显著抑制不同细菌的外排作用,但有 4 种化合物对致病菌大肠杆菌、肠炎沙门氏菌、粪肠球菌和金黄色葡萄球菌的外排泵系统具有特殊的活性。然后,这四种化合物被评估了降低或逆转由特定过度表达的外排泵介导的多药耐药大肠杆菌、沙门氏菌和金黄色葡萄球菌的耐药性的能力。其中一种化合物 2173 可显著降低多药耐药性金黄色葡萄球菌的耐药性。

结论

这些结果表明,化合物 2173 可能可用于治疗由该病原体引起的感染。

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