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In Vitro Activity and In Vivo Efficacy of Cefiderocol against Stenotrophomonas maltophilia

Cefiderocol is a novel siderophore cephalosporin antibiotic with broad coverage against difficult-to-treat Gram-negative bacteria, including those resistant to carbapenems. Its activity against Stenotrophomonas maltophilia was investigated in vitro against clinical isolates and in lung infection mod...

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Autores principales: Nakamura, Rio, Oota, Merime, Matsumoto, Shuhei, Sato, Takafumi, Yamano, Yoshinori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097474/
https://www.ncbi.nlm.nih.gov/pubmed/33526491
http://dx.doi.org/10.1128/AAC.01436-20
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author Nakamura, Rio
Oota, Merime
Matsumoto, Shuhei
Sato, Takafumi
Yamano, Yoshinori
author_facet Nakamura, Rio
Oota, Merime
Matsumoto, Shuhei
Sato, Takafumi
Yamano, Yoshinori
author_sort Nakamura, Rio
collection PubMed
description Cefiderocol is a novel siderophore cephalosporin antibiotic with broad coverage against difficult-to-treat Gram-negative bacteria, including those resistant to carbapenems. Its activity against Stenotrophomonas maltophilia was investigated in vitro against clinical isolates and in lung infection models using strains either resistant (SR202006) or susceptible (SR201934, SR200614) to trimethoprim-sulfamethoxazole. Cefiderocol demonstrated potent in vitro activity against all 217 S. maltophilia clinical isolates tested (MIC(50), 0.063 μg/ml; MIC(90), 0.25 μg/ml). Cefiderocol also demonstrated low MICs against the trimethoprim-sulfamethoxazole-resistant S. maltophilia strains (i.e., SR202006; MIC, 0.125 μg/ml). In a neutropenic mouse lung infection model, cefiderocol (30 mg/kg body weight and 100 mg/kg) demonstrated a significant, dose-dependent reduction in the lung viable bacteria cell count compared with untreated controls in S. maltophilia infection and was the only antibiotic tested to show a similar significant effect in a trimethoprim-sulfamethoxazole-resistant S. maltophilia infection. In immunocompetent rat lung infection models of S. maltophilia, humanized dosing of cefiderocol (2 g every 8 h) and meropenem (1 g every 8 h) revealed pharmacokinetic profiles similar to those in human subjects, and the humanized cefiderocol dosing significantly reduced the lung viable bacteria cell count compared with baseline controls, which received no intervention. Together, the results from these studies suggest that cefiderocol could provide an effective alternative treatment option for S. maltophilia infections in the lower respiratory tract, particularly strains resistant to empirical antibiotics, such as trimethoprim-sulfamethoxazole or minocycline.
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spelling pubmed-80974742021-05-10 In Vitro Activity and In Vivo Efficacy of Cefiderocol against Stenotrophomonas maltophilia Nakamura, Rio Oota, Merime Matsumoto, Shuhei Sato, Takafumi Yamano, Yoshinori Antimicrob Agents Chemother Experimental Therapeutics Cefiderocol is a novel siderophore cephalosporin antibiotic with broad coverage against difficult-to-treat Gram-negative bacteria, including those resistant to carbapenems. Its activity against Stenotrophomonas maltophilia was investigated in vitro against clinical isolates and in lung infection models using strains either resistant (SR202006) or susceptible (SR201934, SR200614) to trimethoprim-sulfamethoxazole. Cefiderocol demonstrated potent in vitro activity against all 217 S. maltophilia clinical isolates tested (MIC(50), 0.063 μg/ml; MIC(90), 0.25 μg/ml). Cefiderocol also demonstrated low MICs against the trimethoprim-sulfamethoxazole-resistant S. maltophilia strains (i.e., SR202006; MIC, 0.125 μg/ml). In a neutropenic mouse lung infection model, cefiderocol (30 mg/kg body weight and 100 mg/kg) demonstrated a significant, dose-dependent reduction in the lung viable bacteria cell count compared with untreated controls in S. maltophilia infection and was the only antibiotic tested to show a similar significant effect in a trimethoprim-sulfamethoxazole-resistant S. maltophilia infection. In immunocompetent rat lung infection models of S. maltophilia, humanized dosing of cefiderocol (2 g every 8 h) and meropenem (1 g every 8 h) revealed pharmacokinetic profiles similar to those in human subjects, and the humanized cefiderocol dosing significantly reduced the lung viable bacteria cell count compared with baseline controls, which received no intervention. Together, the results from these studies suggest that cefiderocol could provide an effective alternative treatment option for S. maltophilia infections in the lower respiratory tract, particularly strains resistant to empirical antibiotics, such as trimethoprim-sulfamethoxazole or minocycline. American Society for Microbiology 2021-03-18 /pmc/articles/PMC8097474/ /pubmed/33526491 http://dx.doi.org/10.1128/AAC.01436-20 Text en Copyright © 2021 Nakamura et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Experimental Therapeutics
Nakamura, Rio
Oota, Merime
Matsumoto, Shuhei
Sato, Takafumi
Yamano, Yoshinori
In Vitro Activity and In Vivo Efficacy of Cefiderocol against Stenotrophomonas maltophilia
title In Vitro Activity and In Vivo Efficacy of Cefiderocol against Stenotrophomonas maltophilia
title_full In Vitro Activity and In Vivo Efficacy of Cefiderocol against Stenotrophomonas maltophilia
title_fullStr In Vitro Activity and In Vivo Efficacy of Cefiderocol against Stenotrophomonas maltophilia
title_full_unstemmed In Vitro Activity and In Vivo Efficacy of Cefiderocol against Stenotrophomonas maltophilia
title_short In Vitro Activity and In Vivo Efficacy of Cefiderocol against Stenotrophomonas maltophilia
title_sort in vitro activity and in vivo efficacy of cefiderocol against stenotrophomonas maltophilia
topic Experimental Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097474/
https://www.ncbi.nlm.nih.gov/pubmed/33526491
http://dx.doi.org/10.1128/AAC.01436-20
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