In vivo efficacy of auranofin in a hamster model of Clostridioides difficile infection

Abstract Clostridioides difficile infections (CDIs) are an urgent public health threat worldwide and are a leading cause of morbidity and mortality in healthcare settings. The increasing incidence and severity of infections combined with the scarcity of effective anti-CDI agents has made treatment o...

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Autores principales: Nader S. Abutaleb, Mohamed N. Seleem
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:0da84e67d61c438098f83388cd1043052021-12-02T14:23:13ZIn vivo efficacy of auranofin in a hamster model of Clostridioides difficile infection10.1038/s41598-021-86595-32045-2322https://doaj.org/article/0da84e67d61c438098f83388cd1043052021-03-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-86595-3https://doaj.org/toc/2045-2322Abstract Clostridioides difficile infections (CDIs) are an urgent public health threat worldwide and are a leading cause of morbidity and mortality in healthcare settings. The increasing incidence and severity of infections combined with the scarcity of effective anti-CDI agents has made treatment of CDI very challenging. Therefore, development of new, effective anticlostridial agents remains a high priority. The current study investigated the in vivo efficacy of auranofin in a CDI hamster model. All hamsters treated with auranofin (5 mg/kg) survived a lethal challenge with C. difficile. Furthermore, auranofin (5 mg/kg) was as effective as vancomycin, the drug of choice for treatment of CDIs, against relapsing CDI. Furthermore, auranofin (5 mg/kg) generated a 3.15-log10 reduction (99.97%) in C. difficile count in the cecal contents of hamsters. These results indicate that auranofin warrants further investigation as a new agent to replenish the pipeline of anti-CDI therapeutics.Nader S. AbutalebMohamed N. SeleemNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Nader S. Abutaleb
Mohamed N. Seleem
In vivo efficacy of auranofin in a hamster model of Clostridioides difficile infection
description Abstract Clostridioides difficile infections (CDIs) are an urgent public health threat worldwide and are a leading cause of morbidity and mortality in healthcare settings. The increasing incidence and severity of infections combined with the scarcity of effective anti-CDI agents has made treatment of CDI very challenging. Therefore, development of new, effective anticlostridial agents remains a high priority. The current study investigated the in vivo efficacy of auranofin in a CDI hamster model. All hamsters treated with auranofin (5 mg/kg) survived a lethal challenge with C. difficile. Furthermore, auranofin (5 mg/kg) was as effective as vancomycin, the drug of choice for treatment of CDIs, against relapsing CDI. Furthermore, auranofin (5 mg/kg) generated a 3.15-log10 reduction (99.97%) in C. difficile count in the cecal contents of hamsters. These results indicate that auranofin warrants further investigation as a new agent to replenish the pipeline of anti-CDI therapeutics.
format article
author Nader S. Abutaleb
Mohamed N. Seleem
author_facet Nader S. Abutaleb
Mohamed N. Seleem
author_sort Nader S. Abutaleb
title In vivo efficacy of auranofin in a hamster model of Clostridioides difficile infection
title_short In vivo efficacy of auranofin in a hamster model of Clostridioides difficile infection
title_full In vivo efficacy of auranofin in a hamster model of Clostridioides difficile infection
title_fullStr In vivo efficacy of auranofin in a hamster model of Clostridioides difficile infection
title_full_unstemmed In vivo efficacy of auranofin in a hamster model of Clostridioides difficile infection
title_sort in vivo efficacy of auranofin in a hamster model of clostridioides difficile infection
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/0da84e67d61c438098f83388cd104305
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AT mohamednseleem invivoefficacyofauranofininahamstermodelofclostridioidesdifficileinfection
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