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分子拓扑学:一种新的抗菌药物耐药性控制策略。

Molecular topology: A new strategy for antimicrobial resistance control.

机构信息

Department of Physical Chemistry, University of Valencia, Avenida V.A. Estelles s/n, 46100 Burjassot, Valencia, Spain.

Department of Physical Chemistry, University of Valencia, Avenida V.A. Estelles s/n, 46100 Burjassot, Valencia, Spain.

出版信息

Eur J Med Chem. 2017 Sep 8;137:233-246. doi: 10.1016/j.ejmech.2017.05.055. Epub 2017 May 30.

Abstract

The control of antimicrobial resistance (AMR) seems to have come to an impasse. The use and abuse of antibacterial drugs has had major consequences on the genetic mutability of both pathogenic and nonpathogenic microorganisms, leading to the development of new highly resistant strains. Because of the complexity of this situation, an in silico strategy based on QSAR molecular topology was devised to identify synthetic molecules as antimicrobial agents not susceptible to one or several mechanisms of resistance such as: biofilms formation (BF), ionophore (IA) activity, epimerase (EI) activity or SOS system (RecA inhibition). After selecting a group of 19 compounds, five of them showed significant antimicrobial activity against several strains of Staphylococcus (2 S. aureus, including 1 methicillin resistant, and 1 S. epidermidis), with MIC values between 16 and 32 mg/L. Among the compounds active on RecA, one showed a marked activity in decreasing RecA gene expression in Escherichia coli.

摘要

抗菌药物的使用和滥用对致病菌和非致病菌的遗传可变性产生了重大影响,导致新的高度耐药菌株的出现。由于这种情况非常复杂,我们设计了一种基于定量构效关系(QSAR)分子拓扑学的计算机模拟策略,以鉴定出不易受生物膜形成(BF)、离子载体(IA)活性、差向异构酶(EI)活性或 SOS 系统(RecA 抑制)等一种或多种耐药机制影响的合成分子作为抗菌剂。在选择了一组 19 种化合物后,其中 5 种对几种金黄色葡萄球菌(包括 1 种耐甲氧西林金黄色葡萄球菌和 1 种表皮葡萄球菌)表现出显著的抗菌活性,MIC 值在 16 至 32mg/L 之间。在对 RecA 有活性的化合物中,有 1 种在降低大肠杆菌 RecA 基因表达方面表现出显著的活性。

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