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Anti-Helicobacter pylori activity of ethoxzolamide
Ethoxzolamide (EZA), acetazolamide, and methazolamide are clinically used sulphonamide drugs designed to treat non-bacteria-related illnesses (e.g. glaucoma), but they also show antimicrobial activity against the gastric pathogen Helicobacter pylori. EZA showed the highest activity, and was effectiv...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759998/ https://www.ncbi.nlm.nih.gov/pubmed/31530039 http://dx.doi.org/10.1080/14756366.2019.1663416 |
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author | Modak, Joyanta K. Tikhomirova, Alexandra Gorrell, Rebecca J. Rahman, Mohammad M. Kotsanas, Despina Korman, Tony M. Garcia-Bustos, Jose Kwok, Terry Ferrero, Richard L. Supuran, Claudiu T. Roujeinikova, Anna |
author_facet | Modak, Joyanta K. Tikhomirova, Alexandra Gorrell, Rebecca J. Rahman, Mohammad M. Kotsanas, Despina Korman, Tony M. Garcia-Bustos, Jose Kwok, Terry Ferrero, Richard L. Supuran, Claudiu T. Roujeinikova, Anna |
author_sort | Modak, Joyanta K. |
collection | PubMed |
description | Ethoxzolamide (EZA), acetazolamide, and methazolamide are clinically used sulphonamide drugs designed to treat non-bacteria-related illnesses (e.g. glaucoma), but they also show antimicrobial activity against the gastric pathogen Helicobacter pylori. EZA showed the highest activity, and was effective against clinical isolates resistant to metronidazole, clarithromycin, and/or amoxicillin, suggesting that EZA kills H. pylori via mechanisms different from that of these antibiotics. The frequency of single-step spontaneous resistance acquisition by H. pylori was less than 5 × 10(−9), showing that resistance to EZA does not develop easily. Resistance was associated with mutations in three genes, including the one that encodes undecaprenyl pyrophosphate synthase, a known target of sulphonamides. The data indicate that EZA impacts multiple targets in killing H. pylori. Our findings suggest that developing the approved anti-glaucoma drug EZA into a more effective anti-H. pylori agent may offer a faster and cost-effective route towards new antimicrobials with a novel mechanism of action. |
format | Online Article Text |
id | pubmed-6759998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-67599982019-10-02 Anti-Helicobacter pylori activity of ethoxzolamide Modak, Joyanta K. Tikhomirova, Alexandra Gorrell, Rebecca J. Rahman, Mohammad M. Kotsanas, Despina Korman, Tony M. Garcia-Bustos, Jose Kwok, Terry Ferrero, Richard L. Supuran, Claudiu T. Roujeinikova, Anna J Enzyme Inhib Med Chem Research Paper Ethoxzolamide (EZA), acetazolamide, and methazolamide are clinically used sulphonamide drugs designed to treat non-bacteria-related illnesses (e.g. glaucoma), but they also show antimicrobial activity against the gastric pathogen Helicobacter pylori. EZA showed the highest activity, and was effective against clinical isolates resistant to metronidazole, clarithromycin, and/or amoxicillin, suggesting that EZA kills H. pylori via mechanisms different from that of these antibiotics. The frequency of single-step spontaneous resistance acquisition by H. pylori was less than 5 × 10(−9), showing that resistance to EZA does not develop easily. Resistance was associated with mutations in three genes, including the one that encodes undecaprenyl pyrophosphate synthase, a known target of sulphonamides. The data indicate that EZA impacts multiple targets in killing H. pylori. Our findings suggest that developing the approved anti-glaucoma drug EZA into a more effective anti-H. pylori agent may offer a faster and cost-effective route towards new antimicrobials with a novel mechanism of action. Taylor & Francis 2019-09-17 /pmc/articles/PMC6759998/ /pubmed/31530039 http://dx.doi.org/10.1080/14756366.2019.1663416 Text en & 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Modak, Joyanta K. Tikhomirova, Alexandra Gorrell, Rebecca J. Rahman, Mohammad M. Kotsanas, Despina Korman, Tony M. Garcia-Bustos, Jose Kwok, Terry Ferrero, Richard L. Supuran, Claudiu T. Roujeinikova, Anna Anti-Helicobacter pylori activity of ethoxzolamide |
title | Anti-Helicobacter pylori activity of ethoxzolamide |
title_full | Anti-Helicobacter pylori activity of ethoxzolamide |
title_fullStr | Anti-Helicobacter pylori activity of ethoxzolamide |
title_full_unstemmed | Anti-Helicobacter pylori activity of ethoxzolamide |
title_short | Anti-Helicobacter pylori activity of ethoxzolamide |
title_sort | anti-helicobacter pylori activity of ethoxzolamide |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759998/ https://www.ncbi.nlm.nih.gov/pubmed/31530039 http://dx.doi.org/10.1080/14756366.2019.1663416 |
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