Metallo-sideromycin as a dual functional complex for combating antimicrobial resistance.
Chenyuan WangYushan XiaRunming WangJingru LiChun-Lung ChanRichard Yi-Tsun KaoPatrick H ToyPak Leung HoHongyan LiHongzhe SunPublished in: Nature communications (2023)
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.
Keyphrases
- gram negative
- multidrug resistant
- antimicrobial resistance
- drug resistant
- pseudomonas aeruginosa
- acinetobacter baumannii
- biofilm formation
- staphylococcus aureus
- escherichia coli
- cystic fibrosis
- induced apoptosis
- candida albicans
- liver failure
- early onset
- cell cycle arrest
- type diabetes
- drug induced
- signaling pathway
- skeletal muscle
- cell proliferation
- risk assessment
- visible light
- binding protein
- bone marrow
- risk factors
- metal organic framework
- insulin resistance
- replacement therapy
- aortic dissection