Multi-target mode of action of silver against Staphylococcus aureus endows it with capability to combat antibiotic resistance

被引:126
|
作者
Wang, Haibo [1 ]
Wang, Minji [2 ,3 ]
Xu, Xiaohan [1 ]
Gao, Peng [4 ]
Xu, Zeling [2 ]
Zhang, Qi [1 ]
Li, Hongyan [1 ]
Yan, Aixin [2 ]
Kao, Richard Yi-Tsun [4 ]
Sun, Hongzhe [1 ]
机构
[1] Univ Hong Kong, Dept Chem, Hong Kong, Peoples R China
[2] Univ Hong Kong, Sch Biol Sci, Hong Kong, Peoples R China
[3] East China Normal Univ, Sch Chem & Mol Engn, Shanghai, Peoples R China
[4] Univ Hong Kong, Dept Microbiol, Hong Kong, Peoples R China
基金
美国国家科学基金会;
关键词
ANTIBACTERIAL ACTION; PROTEOMIC ANALYSIS; DEHYDROGENASE; NANOPARTICLES; MECHANISMS; PROTEINS; TARGETS; BINDING; CELLS; METALLOPROTEINS;
D O I
10.1038/s41467-021-23659-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The rapid emergence of drug resistant Staphylococcus aureus (S. aureus) poses a serious threat to public health globally. Silver (Ag)-based antimicrobials are promising to combat antibiotic resistant S. aureus, yet their molecular targets are largely elusive. Herein, we separate and identify 38 authentic Ag+-binding proteins in S. aureus at the whole-cell scale. We then capture the molecular snapshot on the dynamic action of Ag+ against S. aureus and further validate that Ag+ could inhibit a key target 6-phosphogluconate dehydrogenase through binding to catalytic His185 by X-ray crystallography. Significantly, the multi-target mode of action of Ag+ (and nanosilver) endows its sustainable antimicrobial efficacy, leading to enhanced efficacy of conventional antibiotics and resensitization of MRSA to antibiotics. Our study resolves the long-standing question of the molecular targets of silver in S. aureus and offers insights into the sustainable bacterial susceptibility of silver, providing a potential approach for combating antimicrobial resistance. Silver (Ag) has been used as an antimicrobial agent since a long time, but its molecular mechanism of action was not elucidated due to technical challenges. Here, the authors develop a mass spectrometric approach to identify the Ag-proteome in Staphylococcus aureus, and capture a molecular snapshot of the dynamic bactericidal mode of action of Ag through targeting multiple biological pathways.
引用
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页数:16
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