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

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-negat...

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Autores principales: Wang, Chenyuan, Xia, Yushan, Wang, Runming, Li, Jingru, Chan, Chun-Lung, Kao, Richard Yi-Tsun, Toy, Patrick H., Ho, Pak-Leung, Li, Hongyan, Sun, Hongzhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474269/
https://www.ncbi.nlm.nih.gov/pubmed/37658047
http://dx.doi.org/10.1038/s41467-023-40828-3
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author Wang, Chenyuan
Xia, Yushan
Wang, Runming
Li, Jingru
Chan, Chun-Lung
Kao, Richard Yi-Tsun
Toy, Patrick H.
Ho, Pak-Leung
Li, Hongyan
Sun, Hongzhe
author_facet Wang, Chenyuan
Xia, Yushan
Wang, Runming
Li, Jingru
Chan, Chun-Lung
Kao, Richard Yi-Tsun
Toy, Patrick H.
Ho, Pak-Leung
Li, Hongyan
Sun, Hongzhe
author_sort Wang, Chenyuan
collection PubMed
description 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 Bi(3+) to cefiderocol with Fe(3+), leading to enhanced uptake of Bi(3+) and reduced levels of Fe(3+) in cells. Our studies provide insight into the antimicrobial potential of metallo-sideromycins.
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spelling pubmed-104742692023-09-03 Metallo-sideromycin as a dual functional complex for combating antimicrobial resistance Wang, Chenyuan Xia, Yushan Wang, Runming Li, Jingru Chan, Chun-Lung Kao, Richard Yi-Tsun Toy, Patrick H. Ho, Pak-Leung Li, Hongyan Sun, Hongzhe Nat Commun Article 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 Bi(3+) to cefiderocol with Fe(3+), leading to enhanced uptake of Bi(3+) and reduced levels of Fe(3+) in cells. Our studies provide insight into the antimicrobial potential of metallo-sideromycins. Nature Publishing Group UK 2023-09-01 /pmc/articles/PMC10474269/ /pubmed/37658047 http://dx.doi.org/10.1038/s41467-023-40828-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Chenyuan
Xia, Yushan
Wang, Runming
Li, Jingru
Chan, Chun-Lung
Kao, Richard Yi-Tsun
Toy, Patrick H.
Ho, Pak-Leung
Li, Hongyan
Sun, Hongzhe
Metallo-sideromycin as a dual functional complex for combating antimicrobial resistance
title Metallo-sideromycin as a dual functional complex for combating antimicrobial resistance
title_full Metallo-sideromycin as a dual functional complex for combating antimicrobial resistance
title_fullStr Metallo-sideromycin as a dual functional complex for combating antimicrobial resistance
title_full_unstemmed Metallo-sideromycin as a dual functional complex for combating antimicrobial resistance
title_short Metallo-sideromycin as a dual functional complex for combating antimicrobial resistance
title_sort metallo-sideromycin as a dual functional complex for combating antimicrobial resistance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474269/
https://www.ncbi.nlm.nih.gov/pubmed/37658047
http://dx.doi.org/10.1038/s41467-023-40828-3
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