In vivo efficacy of auranofin in a hamster model of Clostridioides difficile infection
dc.contributor.author | Abutaleb, Nader S. | en |
dc.contributor.author | Seleem, Mohamed N. | en |
dc.contributor.department | Biomedical Sciences and Pathobiology | en |
dc.date.accessioned | 2021-08-18T18:59:26Z | en |
dc.date.available | 2021-08-18T18:59:26Z | en |
dc.date.issued | 2021-03-29 | en |
dc.date.updated | 2021-08-18T18:59:23Z | en |
dc.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. | en |
dc.description.version | Published version | en |
dc.format.extent | 7 page(s) | en |
dc.format.mimetype | application/pdf | en |
dc.identifier | ARTN 7093 (Article number) | en |
dc.identifier.doi | https://doi.org/10.1038/s41598-021-86595-3 | en |
dc.identifier.eissn | 2045-2322 | en |
dc.identifier.issn | 2045-2322 | en |
dc.identifier.issue | 1 | en |
dc.identifier.orcid | Seleem, Mohamed [0000-0003-0939-0458] | en |
dc.identifier.other | 10.1038/s41598-021-86595-3 (PII) | en |
dc.identifier.pmid | 33782498 (pubmed) | en |
dc.identifier.uri | http://hdl.handle.net/10919/104672 | en |
dc.identifier.volume | 11 | en |
dc.language.iso | en | en |
dc.publisher | Nature Research | en |
dc.relation.uri | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000636358400036&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=930d57c9ac61a043676db62af60056c1 | en |
dc.rights | Creative Commons Attribution 4.0 International | en |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | en |
dc.subject | TREATMENT FAILURE | en |
dc.subject | 1ST RECURRENCE | en |
dc.subject | FIDAXOMICIN | en |
dc.subject | DIARRHEA | en |
dc.subject | METRONIDAZOLE | en |
dc.subject | VANCOMYCIN | en |
dc.subject | AGENT | en |
dc.subject | EPIDEMIOLOGY | en |
dc.subject | GUIDELINES | en |
dc.subject | RESISTANCE | en |
dc.title | In vivo efficacy of auranofin in a hamster model of Clostridioides difficile infection | en |
dc.title.serial | Scientific Reports | en |
dc.type | Article - Refereed | en |
dc.type.dcmitype | Text | en |
dc.type.other | Article | en |
dc.type.other | Journal | en |
dcterms.dateAccepted | 2021-03-10 | en |
pubs.organisational-group | /Virginia Tech | en |
pubs.organisational-group | /Virginia Tech/Veterinary Medicine | en |
pubs.organisational-group | /Virginia Tech/Veterinary Medicine/Biomedical Sciences and Pathobiology | en |
pubs.organisational-group | /Virginia Tech/Faculty of Health Sciences | en |
pubs.organisational-group | /Virginia Tech/All T&R Faculty | en |
pubs.organisational-group | /Virginia Tech/Veterinary Medicine/CVM T&R Faculty | en |
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