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

Author

Listed:
  • Haibo Wang

    (The University of Hong Kong)

  • Minji Wang

    (The University of Hong Kong
    East China Normal University)

  • Xiaohan Xu

    (The University of Hong Kong)

  • Peng Gao

    (The University of Hong Kong)

  • Zeling Xu

    (The University of Hong Kong)

  • Qi Zhang

    (The University of Hong Kong)

  • Hongyan Li

    (The University of Hong Kong)

  • Aixin Yan

    (The University of Hong Kong)

  • Richard Yi-Tsun Kao

    (The University of Hong Kong)

  • Hongzhe Sun

    (The University of Hong Kong)

Abstract

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.

Suggested Citation

  • Haibo Wang & Minji Wang & Xiaohan Xu & Peng Gao & Zeling Xu & Qi Zhang & Hongyan Li & Aixin Yan & Richard Yi-Tsun Kao & Hongzhe Sun, 2021. "Multi-target mode of action of silver against Staphylococcus aureus endows it with capability to combat antibiotic resistance," Nature Communications, Nature, vol. 12(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-23659-y
    DOI: 10.1038/s41467-021-23659-y
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    Cited by:

    1. Xueqin Shu & Yingying Shi & Yi Huang & Dan Yu & Baolin Sun, 2023. "Transcription tuned by S-nitrosylation underlies a mechanism for Staphylococcus aureus to circumvent vancomycin killing," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    2. Bang Lin Li & Jun Jiang Luo & Hao Lin Zou & Qing-Meng Zhang & Liu-Bin Zhao & Hang Qian & Hong Qun Luo & David Tai Leong & Nian Bing Li, 2022. "Chiral nanocrystals grown from MoS2 nanosheets enable photothermally modulated enantioselective release of antimicrobial drugs," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    3. Chenyuan Wang & Yushan Xia & Runming Wang & Jingru Li & Chun-Lung Chan & Richard Yi-Tsun Kao & Patrick H. Toy & Pak-Leung Ho & Hongyan Li & Hongzhe Sun, 2023. "Metallo-sideromycin as a dual functional complex for combating antimicrobial resistance," Nature Communications, Nature, vol. 14(1), pages 1-11, December.

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