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基于表面等离子体共振的磺胺类药物与群体感应抑制剂对大肠杆菌联合毒性的机制研究

A SAR-based mechanistic study on the combined toxicities of sulfonamides and quorum sensing inhibitors on Escherichia coli.

作者信息

Chen C, Wang D, Wang H, Lin Z, Fang Z

机构信息

a State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering , Tongji University , Shanghai , China.

b Post-doctoral Research Station, College of Civil Engineering , Tongji University , Shanghai , China.

出版信息

SAR QSAR Environ Res. 2017 Jul;28(7):595-608. doi: 10.1080/1062936X.2017.1354914.

Abstract

Quorum sensing inhibitors (QSIs) are promising alternatives to antibiotics, but they are discharged into the environment after their use cycle. This poses joint effects on the organisms in the environment. Therefore, it is of great importance to study the combined toxicities of QSIs and antibiotics. In this study, we investigated the single and combined toxicities of four potential QSIs and 11 sulfonamides (SAs) on Escherichia coli. The results revealed that the single toxicities of SAs were greater than those of QSIs, and the toxicities were found positively related to the binding energies (E) with their target proteins, for both antibiotics and QSIs. The combined toxicities of the binary mixtures were observed to be either antagonism or addition. The antagonism could be explained by the phenomenon that QSIs changed SAs molecules into ionic forms, preventing the SA molecules entering the bacteria. Furthermore, it was found that the ratios of the effective concentration (the actual concentration involved in the interaction with the proteins) in the antagonistic cases were higher than those in the additive cases. This study would benefit both rational use of the drug combination and ecological risk assessment of antibiotics and QSIs in the real environment.

摘要

群体感应抑制剂(QSIs)是抗生素的有前景的替代品,但在其使用周期结束后会排放到环境中。这对环境中的生物产生联合效应。因此,研究QSIs与抗生素的联合毒性非常重要。在本研究中,我们调查了四种潜在QSIs和11种磺胺类药物(SAs)对大肠杆菌的单一毒性和联合毒性。结果表明,SAs的单一毒性大于QSIs,并且发现无论是抗生素还是QSIs,其毒性都与它们与靶蛋白的结合能(E)呈正相关。二元混合物的联合毒性观察到为拮抗或相加作用。拮抗作用可以用QSIs将SAs分子转变为离子形式,阻止SA分子进入细菌这一现象来解释。此外,发现拮抗情况下有效浓度(与蛋白质相互作用中涉及的实际浓度)的比值高于相加情况下的比值。本研究将有助于合理使用药物组合以及对实际环境中抗生素和QSIs进行生态风险评估。

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