Repurposing Clinical Molecule Ebselen to Combat Drug Resistant Pathogens.

Without a doubt, our current antimicrobials are losing the battle in the fight against newly-emerged multidrug-resistant pathogens. There is a pressing, unmet need for novel antimicrobials and novel approaches to develop them; however, it is becoming increasingly difficult and costly to develop new...

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Main Authors: Shankar Thangamani, Waleed Younis, Mohamed N Seleem
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4519285?pdf=render
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spelling doaj-17c1eab1b5c9453d88eab204b8db71f22020-11-25T02:47:03ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01107e013387710.1371/journal.pone.0133877Repurposing Clinical Molecule Ebselen to Combat Drug Resistant Pathogens.Shankar ThangamaniWaleed YounisMohamed N SeleemWithout a doubt, our current antimicrobials are losing the battle in the fight against newly-emerged multidrug-resistant pathogens. There is a pressing, unmet need for novel antimicrobials and novel approaches to develop them; however, it is becoming increasingly difficult and costly to develop new antimicrobials. One strategy to reduce the time and cost associated with antimicrobial innovation is drug repurposing, which is to find new applications outside the scope of the original medical indication of the drug. Ebselen, an organoselenium clinical molecule, possesses potent antimicrobial activity against clinical multidrug-resistant Gram-positive pathogens, including Staphylococcus, Streptococcus, and Enterococcus, but not against Gram-negative pathogens. Moreover, the activity of ebselen against Gram-positive pathogens exceeded those activities determined for vancomycin and linezolid, drugs of choice for treatment of Enterococcus and Staphylococcus infections. The minimum inhibitory concentrations of ebselen at which 90% of clinical isolates of Enterococcus and Staphylococcus were inhibited (MIC90) were found to be 0.5 and 0.25 mg/L, respectively. Ebselen showed significant clearance of intracellular methicillin-resistant S. aureus (MRSA) in comparison to vancomycin and linezolid. We demonstrated that ebselen inhibits the bacterial translation process without affecting mitochondrial biogenesis. Additionally, ebselen was found to exhibit excellent activity in vivo in a Caenorhabditis elegans MRSA-infected whole animal model. Finally, ebselen showed synergistic activities with conventional antimicrobials against MRSA. Taken together, our results demonstrate that ebselen, with its potent antimicrobial activity and safety profiles, can be potentially used to treat multidrug resistant Gram-positive bacterial infections alone or in combination with other antibiotics and should be further clinically evaluated.http://europepmc.org/articles/PMC4519285?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Shankar Thangamani
Waleed Younis
Mohamed N Seleem
spellingShingle Shankar Thangamani
Waleed Younis
Mohamed N Seleem
Repurposing Clinical Molecule Ebselen to Combat Drug Resistant Pathogens.
PLoS ONE
author_facet Shankar Thangamani
Waleed Younis
Mohamed N Seleem
author_sort Shankar Thangamani
title Repurposing Clinical Molecule Ebselen to Combat Drug Resistant Pathogens.
title_short Repurposing Clinical Molecule Ebselen to Combat Drug Resistant Pathogens.
title_full Repurposing Clinical Molecule Ebselen to Combat Drug Resistant Pathogens.
title_fullStr Repurposing Clinical Molecule Ebselen to Combat Drug Resistant Pathogens.
title_full_unstemmed Repurposing Clinical Molecule Ebselen to Combat Drug Resistant Pathogens.
title_sort repurposing clinical molecule ebselen to combat drug resistant pathogens.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Without a doubt, our current antimicrobials are losing the battle in the fight against newly-emerged multidrug-resistant pathogens. There is a pressing, unmet need for novel antimicrobials and novel approaches to develop them; however, it is becoming increasingly difficult and costly to develop new antimicrobials. One strategy to reduce the time and cost associated with antimicrobial innovation is drug repurposing, which is to find new applications outside the scope of the original medical indication of the drug. Ebselen, an organoselenium clinical molecule, possesses potent antimicrobial activity against clinical multidrug-resistant Gram-positive pathogens, including Staphylococcus, Streptococcus, and Enterococcus, but not against Gram-negative pathogens. Moreover, the activity of ebselen against Gram-positive pathogens exceeded those activities determined for vancomycin and linezolid, drugs of choice for treatment of Enterococcus and Staphylococcus infections. The minimum inhibitory concentrations of ebselen at which 90% of clinical isolates of Enterococcus and Staphylococcus were inhibited (MIC90) were found to be 0.5 and 0.25 mg/L, respectively. Ebselen showed significant clearance of intracellular methicillin-resistant S. aureus (MRSA) in comparison to vancomycin and linezolid. We demonstrated that ebselen inhibits the bacterial translation process without affecting mitochondrial biogenesis. Additionally, ebselen was found to exhibit excellent activity in vivo in a Caenorhabditis elegans MRSA-infected whole animal model. Finally, ebselen showed synergistic activities with conventional antimicrobials against MRSA. Taken together, our results demonstrate that ebselen, with its potent antimicrobial activity and safety profiles, can be potentially used to treat multidrug resistant Gram-positive bacterial infections alone or in combination with other antibiotics and should be further clinically evaluated.
url http://europepmc.org/articles/PMC4519285?pdf=render
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AT mohamednseleem repurposingclinicalmoleculeebselentocombatdrugresistantpathogens
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