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Resensitization of methicillin-resistant Staphylococcus aureus by amoxapine, an FDA-approved antidepressant

The rapid increase in bacterial resistance to antibiotics is a global healthcare crisis. Non-antibiotic pharmaceuticals that have attained approval by the United States Food and Drug Administration have the potential to be repurposed as bacterial resistance-modifying agents and therefore could becom...

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Detalles Bibliográficos
Autores principales: Wilson, Tyler J., Blackledge, Meghan S., Vigueira, Patrick A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767979/
https://www.ncbi.nlm.nih.gov/pubmed/29349359
http://dx.doi.org/10.1016/j.heliyon.2017.e00501
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author Wilson, Tyler J.
Blackledge, Meghan S.
Vigueira, Patrick A.
author_facet Wilson, Tyler J.
Blackledge, Meghan S.
Vigueira, Patrick A.
author_sort Wilson, Tyler J.
collection PubMed
description The rapid increase in bacterial resistance to antibiotics is a global healthcare crisis. Non-antibiotic pharmaceuticals that have attained approval by the United States Food and Drug Administration have the potential to be repurposed as bacterial resistance-modifying agents and therefore could become valuable resources in our battle against antibiotic-resistant microbes. Amoxapine is a tetracyclic antidepressant used in the treatment of major depressive disorder. Here we demonstrate the ability of amoxapine to resensitize methicillin-resistant Staphylococcus aureus strain ATCC 43300 to oxacillin in both agar diffusion and broth microdilution assays. Amoxapine also reduced the bacterial cleavage of nitrocefin in a dose-dependent manner, suggesting that it may exert its adjuvant effects through reduction of beta-lactamase activity.
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spelling pubmed-57679792018-01-18 Resensitization of methicillin-resistant Staphylococcus aureus by amoxapine, an FDA-approved antidepressant Wilson, Tyler J. Blackledge, Meghan S. Vigueira, Patrick A. Heliyon Article The rapid increase in bacterial resistance to antibiotics is a global healthcare crisis. Non-antibiotic pharmaceuticals that have attained approval by the United States Food and Drug Administration have the potential to be repurposed as bacterial resistance-modifying agents and therefore could become valuable resources in our battle against antibiotic-resistant microbes. Amoxapine is a tetracyclic antidepressant used in the treatment of major depressive disorder. Here we demonstrate the ability of amoxapine to resensitize methicillin-resistant Staphylococcus aureus strain ATCC 43300 to oxacillin in both agar diffusion and broth microdilution assays. Amoxapine also reduced the bacterial cleavage of nitrocefin in a dose-dependent manner, suggesting that it may exert its adjuvant effects through reduction of beta-lactamase activity. Elsevier 2018-01-12 /pmc/articles/PMC5767979/ /pubmed/29349359 http://dx.doi.org/10.1016/j.heliyon.2017.e00501 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Wilson, Tyler J.
Blackledge, Meghan S.
Vigueira, Patrick A.
Resensitization of methicillin-resistant Staphylococcus aureus by amoxapine, an FDA-approved antidepressant
title Resensitization of methicillin-resistant Staphylococcus aureus by amoxapine, an FDA-approved antidepressant
title_full Resensitization of methicillin-resistant Staphylococcus aureus by amoxapine, an FDA-approved antidepressant
title_fullStr Resensitization of methicillin-resistant Staphylococcus aureus by amoxapine, an FDA-approved antidepressant
title_full_unstemmed Resensitization of methicillin-resistant Staphylococcus aureus by amoxapine, an FDA-approved antidepressant
title_short Resensitization of methicillin-resistant Staphylococcus aureus by amoxapine, an FDA-approved antidepressant
title_sort resensitization of methicillin-resistant staphylococcus aureus by amoxapine, an fda-approved antidepressant
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767979/
https://www.ncbi.nlm.nih.gov/pubmed/29349359
http://dx.doi.org/10.1016/j.heliyon.2017.e00501
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