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Metallo-sideromycin as a dual functional complex for combating antimicrobial resistance

Author

Listed:
  • Chenyuan Wang

    (The University of Hong Kong)

  • Yushan Xia

    (The University of Hong Kong)

  • Runming Wang

    (The University of Hong Kong)

  • Jingru Li

    (The University of Hong Kong
    Chemistry and Chemical Engineering Guangdong Laboratory)

  • Chun-Lung Chan

    (The University of Hong Kong)

  • Richard Yi-Tsun Kao

    (The University of Hong Kong)

  • Patrick H. Toy

    (The University of Hong Kong)

  • Pak-Leung Ho

    (The University of Hong Kong
    The University of Hong Kong)

  • Hongyan Li

    (The University of Hong Kong
    The University of Hong Kong)

  • Hongzhe Sun

    (The University of Hong Kong
    The University of Hong Kong)

Abstract

The rapid emergence of antimicrobial resistance (AMR) pathogens highlights the urgent need to approach this global burden with alternative strategies. Cefiderocol (Fetroja®) is a clinically-used sideromycin, that is utilized for the treatment of severe drug-resistant infections, caused by Gram-negative bacteria; there is evidence of cefiderocol-resistance occurring in bacterial strains however. To increase the efficacy and extend the life-span of sideromycins, we demonstrate strong synergisms between cefiderocol and metallodrugs (e.g., colloidal bismuth citrate (CBS)), against Pseudomonas aeruginosa and Burkholderia cepacia. Moreover, CBS enhances cefiderocol efficacy against biofilm formation, suppresses the resistance development in P. aeruginosa and resensitizes clinically isolated resistant P. aeruginosa to cefiderocol. Notably, the co-therapy of CBS and cefiderocol significantly increases the survival rate of mice and decreases bacterial loads in the lung in a murine acute pneumonia model. The observed phenomena are partially attributable to the competitive binding of Bi3+ to cefiderocol with Fe3+, leading to enhanced uptake of Bi3+ and reduced levels of Fe3+ in cells. Our studies provide insight into the antimicrobial potential of metallo-sideromycins.

Suggested Citation

  • 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.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-40828-3
    DOI: 10.1038/s41467-023-40828-3
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    References listed on IDEAS

    as
    1. Haibo Wang & Minji Wang & Xiaohan Xu & Peng Gao & Zeling Xu & Qi Zhang & Hongyan Li & Aixin Yan & Richard Yi-Tsun Kao & Hongzhe Sun, 2021. "Author Correction: 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 1-1, December.
    2. 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.
    3. Runming Wang & Tsz-Pui Lai & Peng Gao & Hongmin Zhang & Pak-Leung Ho & Patrick Chiu-Yat Woo & Guixing Ma & Richard Yi-Tsun Kao & Hongyan Li & Hongzhe Sun, 2018. "Bismuth antimicrobial drugs serve as broad-spectrum metallo-β-lactamase inhibitors," Nature Communications, Nature, vol. 9(1), pages 1-12, December.
    4. Eric D. Brown & Gerard D. Wright, 2016. "Antibacterial drug discovery in the resistance era," Nature, Nature, vol. 529(7586), pages 336-343, January.
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