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Cefiderocol is an effective topical monotherapy for experimental extensively-drug resistant Pseudomonas aeruginosa keratitis

PURPOSE: To test cefiderocol, a siderophore-cephalosporin antibiotic for topical monotherapy treatment of experimental extensively drug resistant (XDR) Pseudomonas aeruginosa keratitis. DESIGN: Preclinical study. SUBJECTS AND CONTROLS: Deidentified P. aeruginosa keratitis isolates, XDR P. aeruginosa...

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Autores principales: Romanowski, Eric G., Mumper, Sonya M., Shanks, Hazel Q., Yates, Kathleen A., Mandell, Jonathan B., Zegans, Michael E., Shanks, Robert M. Q.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491197/
https://www.ncbi.nlm.nih.gov/pubmed/37693441
http://dx.doi.org/10.1101/2023.08.31.555778
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author Romanowski, Eric G.
Mumper, Sonya M.
Shanks, Hazel Q.
Yates, Kathleen A.
Mandell, Jonathan B.
Zegans, Michael E.
Shanks, Robert M. Q.
author_facet Romanowski, Eric G.
Mumper, Sonya M.
Shanks, Hazel Q.
Yates, Kathleen A.
Mandell, Jonathan B.
Zegans, Michael E.
Shanks, Robert M. Q.
author_sort Romanowski, Eric G.
collection PubMed
description PURPOSE: To test cefiderocol, a siderophore-cephalosporin antibiotic for topical monotherapy treatment of experimental extensively drug resistant (XDR) Pseudomonas aeruginosa keratitis. DESIGN: Preclinical study. SUBJECTS AND CONTROLS: Deidentified P. aeruginosa keratitis isolates, XDR P. aeruginosa from eye drop outbreak, rabbits, saline, cefiderocol 50 mg/ml, ciprofloxacin 0.3%, and tobramycin 14 mg/ml. METHODS, INTERVENTION, OR TESTING: Cefiderocol antibacterial activity against P. aeruginosa keratitis isolates (n=135) was evaluated by minimum inhibitory concentration (MIC) testing. Ocular toxicity/tolerability and antibacterial efficacy were tested in vivo with experimental rabbit models. Corneal concentrations and stability were assessed using a bioassay. MAIN OUTCOME MEASURES: MIC analysis for susceptibility, graded tests for ocular toxicity/tolerability, CFU analysis for bacterial burden, corneal cefiderocol concentrations. RESULTS: 100% of P. aeruginosa keratitis isolates were susceptible to cefiderocol (n=135), the MIC(90) was 0.125 μg/ml including the XDR isolate (MIC = 0.125 μg/ml). Topical cefiderocol 50 mg/ml was minimally toxic to the ocular surface and was well tolerated. For the XDR P. aeruginosa isolate, topical cefiderocol 50 mg/ml, significantly decreased corneal CFU compared to ciprofloxacin 0.3%, tobramycin 14 mg/ml, and saline. In addition, tobramycin 14 mg/ml was more effective than the saline control. Mean cefiderocol corneal concentrations were 191x greater than the MIC(90) of the P. aeruginosa keratitis isolates. Refrigerated cefiderocol maintained antimicrobial activity over a one-month period. CONCLUSIONS: These results demonstrate that cefiderocol is well tolerated on rabbit corneas and is effective against P. aeruginosa keratitis isolates in vitro and was effective in vivo against an XDR isolate in a rabbit keratitis model. Given the recent outbreak of keratitis caused by this XDR P. aeruginosa, cefiderocol is a promising additional antibiotic that should be further evaluated for topical treatment of keratitis caused by antibiotic resistant P. aeruginosa.
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spelling pubmed-104911972023-09-09 Cefiderocol is an effective topical monotherapy for experimental extensively-drug resistant Pseudomonas aeruginosa keratitis Romanowski, Eric G. Mumper, Sonya M. Shanks, Hazel Q. Yates, Kathleen A. Mandell, Jonathan B. Zegans, Michael E. Shanks, Robert M. Q. bioRxiv Article PURPOSE: To test cefiderocol, a siderophore-cephalosporin antibiotic for topical monotherapy treatment of experimental extensively drug resistant (XDR) Pseudomonas aeruginosa keratitis. DESIGN: Preclinical study. SUBJECTS AND CONTROLS: Deidentified P. aeruginosa keratitis isolates, XDR P. aeruginosa from eye drop outbreak, rabbits, saline, cefiderocol 50 mg/ml, ciprofloxacin 0.3%, and tobramycin 14 mg/ml. METHODS, INTERVENTION, OR TESTING: Cefiderocol antibacterial activity against P. aeruginosa keratitis isolates (n=135) was evaluated by minimum inhibitory concentration (MIC) testing. Ocular toxicity/tolerability and antibacterial efficacy were tested in vivo with experimental rabbit models. Corneal concentrations and stability were assessed using a bioassay. MAIN OUTCOME MEASURES: MIC analysis for susceptibility, graded tests for ocular toxicity/tolerability, CFU analysis for bacterial burden, corneal cefiderocol concentrations. RESULTS: 100% of P. aeruginosa keratitis isolates were susceptible to cefiderocol (n=135), the MIC(90) was 0.125 μg/ml including the XDR isolate (MIC = 0.125 μg/ml). Topical cefiderocol 50 mg/ml was minimally toxic to the ocular surface and was well tolerated. For the XDR P. aeruginosa isolate, topical cefiderocol 50 mg/ml, significantly decreased corneal CFU compared to ciprofloxacin 0.3%, tobramycin 14 mg/ml, and saline. In addition, tobramycin 14 mg/ml was more effective than the saline control. Mean cefiderocol corneal concentrations were 191x greater than the MIC(90) of the P. aeruginosa keratitis isolates. Refrigerated cefiderocol maintained antimicrobial activity over a one-month period. CONCLUSIONS: These results demonstrate that cefiderocol is well tolerated on rabbit corneas and is effective against P. aeruginosa keratitis isolates in vitro and was effective in vivo against an XDR isolate in a rabbit keratitis model. Given the recent outbreak of keratitis caused by this XDR P. aeruginosa, cefiderocol is a promising additional antibiotic that should be further evaluated for topical treatment of keratitis caused by antibiotic resistant P. aeruginosa. Cold Spring Harbor Laboratory 2023-09-02 /pmc/articles/PMC10491197/ /pubmed/37693441 http://dx.doi.org/10.1101/2023.08.31.555778 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Romanowski, Eric G.
Mumper, Sonya M.
Shanks, Hazel Q.
Yates, Kathleen A.
Mandell, Jonathan B.
Zegans, Michael E.
Shanks, Robert M. Q.
Cefiderocol is an effective topical monotherapy for experimental extensively-drug resistant Pseudomonas aeruginosa keratitis
title Cefiderocol is an effective topical monotherapy for experimental extensively-drug resistant Pseudomonas aeruginosa keratitis
title_full Cefiderocol is an effective topical monotherapy for experimental extensively-drug resistant Pseudomonas aeruginosa keratitis
title_fullStr Cefiderocol is an effective topical monotherapy for experimental extensively-drug resistant Pseudomonas aeruginosa keratitis
title_full_unstemmed Cefiderocol is an effective topical monotherapy for experimental extensively-drug resistant Pseudomonas aeruginosa keratitis
title_short Cefiderocol is an effective topical monotherapy for experimental extensively-drug resistant Pseudomonas aeruginosa keratitis
title_sort cefiderocol is an effective topical monotherapy for experimental extensively-drug resistant pseudomonas aeruginosa keratitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491197/
https://www.ncbi.nlm.nih.gov/pubmed/37693441
http://dx.doi.org/10.1101/2023.08.31.555778
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