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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Veröffentlicht in:Nature communications 2023-09, Vol.14 (1), p.5311-5311, Article 5311
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung: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. Here, the authors utilise cefiderocol, a sideromycin, in complex with colloidal bismuth citrate, to demonstrate antimicrobial efficacy against Pseudomonas aeruginosa in vivo.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-023-40828-3