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A new coumarin compound DCH combats methicillin-resistant Staphylococcus aureus biofilm by targeting arginine repressor.


ABSTRACT: Staphylococcus aureus infection is difficult to eradicate because of biofilm formation and antibiotic resistance. The increasing prevalence of methicillin-resistant Staphylococcus aureus (MRSA) infection necessitates the development of a new agent against bacterial biofilms. We report a new coumarin compound, termed DCH, that effectively combats MRSA in vitro and in vivo and exhibits potent antibiofilm activity without detectable resistance. Cellular proteome analysis suggests that the molecular mechanism of action of DCH involves the arginine catabolic pathway. Using molecular docking and binding affinity assays of DCH, and comparison of the properties of wild-type and ArgR-deficient MRSA strains, we demonstrate that the arginine repressor ArgR, an essential regulator of the arginine catabolic pathway, is the target of DCH. These findings indicate that DCH is a promising lead compound and validate bacterial ArgR as a potential target in the development of new drugs against MRSA biofilms.

SUBMITTER: Qu D 

PROVIDER: S-EPMC7439407 | biostudies-literature | 2020 Jul

REPOSITORIES: biostudies-literature

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A new coumarin compound DCH combats methicillin-resistant <i>Staphylococcus aureus</i> biofilm by targeting arginine repressor.

Qu Di D   Hou Zheng Z   Li Jing J   Luo Liyang L   Su Shan S   Ye Zichen Z   Bai Yinlan Y   Zhang Xinlei X   Chen Guanghui G   Li Zhoupeng Z   Wang Yikun Y   Xue Xiaoyan X   Luo Xiaoxing X   Li Mingkai M  

Science advances 20200722 30


<i>Staphylococcus aureus</i> infection is difficult to eradicate because of biofilm formation and antibiotic resistance. The increasing prevalence of methicillin-resistant <i>Staphylococcus aureus</i> (MRSA) infection necessitates the development of a new agent against bacterial biofilms. We report a new coumarin compound, termed DCH, that effectively combats MRSA in vitro and in vivo and exhibits potent antibiofilm activity without detectable resistance. Cellular proteome analysis suggests that  ...[more]

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