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Preclinical development of Ramizol, an antibiotic belonging to a new class, for the treatment of Clostridium difficile colitis
Antibiotic-resistant bacteria is a major threat to human health and is predicted to become the leading cause of death from disease by 2050. Despite the recent resurgence of research and development in the area, few antibiotics have reached the market, with most of the recently approved antibiotics c...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399159/ https://www.ncbi.nlm.nih.gov/pubmed/27189122 http://dx.doi.org/10.1038/ja.2016.45 |
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author | Rao, Shasha Prestidge, Clive A Miesel, Lynn Sweeney, Deb Shinabarger, Dean L Boulos, Ramiz A |
author_facet | Rao, Shasha Prestidge, Clive A Miesel, Lynn Sweeney, Deb Shinabarger, Dean L Boulos, Ramiz A |
author_sort | Rao, Shasha |
collection | PubMed |
description | Antibiotic-resistant bacteria is a major threat to human health and is predicted to become the leading cause of death from disease by 2050. Despite the recent resurgence of research and development in the area, few antibiotics have reached the market, with most of the recently approved antibiotics corresponding to new uses for old antibiotics, or structurally similar derivatives thereof. We have recently reported an in silico approach that led to the design of an entirely new class of antibiotics for the bacteria-specific mechanosensitive ion channel of large conductance: MscL. Here, we present the preclinical development of one such antibiotic, Ramizol, a first generation antibiotic belonging to that class. We present the lack of interaction between Ramizol and other mammalian channels adding credibility to its MscL selectivity. We determine the pharmacokinetic profile in a rat model and show <0.1% of Ramizol is absorbed systemically. We show this non-systemic nature of the antibiotic translates to over 70% survival of hamsters in a Clostridium difficile colitis model. Lastly, initial in vitro data indicate that resistance to Ramizol occurs at a low frequency. In conclusion, we establish the potential of Ramizol as an effective new treatment for C. difficile associated disease. |
format | Online Article Text |
id | pubmed-5399159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53991592017-05-09 Preclinical development of Ramizol, an antibiotic belonging to a new class, for the treatment of Clostridium difficile colitis Rao, Shasha Prestidge, Clive A Miesel, Lynn Sweeney, Deb Shinabarger, Dean L Boulos, Ramiz A J Antibiot (Tokyo) Original Article Antibiotic-resistant bacteria is a major threat to human health and is predicted to become the leading cause of death from disease by 2050. Despite the recent resurgence of research and development in the area, few antibiotics have reached the market, with most of the recently approved antibiotics corresponding to new uses for old antibiotics, or structurally similar derivatives thereof. We have recently reported an in silico approach that led to the design of an entirely new class of antibiotics for the bacteria-specific mechanosensitive ion channel of large conductance: MscL. Here, we present the preclinical development of one such antibiotic, Ramizol, a first generation antibiotic belonging to that class. We present the lack of interaction between Ramizol and other mammalian channels adding credibility to its MscL selectivity. We determine the pharmacokinetic profile in a rat model and show <0.1% of Ramizol is absorbed systemically. We show this non-systemic nature of the antibiotic translates to over 70% survival of hamsters in a Clostridium difficile colitis model. Lastly, initial in vitro data indicate that resistance to Ramizol occurs at a low frequency. In conclusion, we establish the potential of Ramizol as an effective new treatment for C. difficile associated disease. Nature Publishing Group 2016-12 2016-05-18 /pmc/articles/PMC5399159/ /pubmed/27189122 http://dx.doi.org/10.1038/ja.2016.45 Text en Copyright © 2016 Japan Antibiotics Research Association http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Original Article Rao, Shasha Prestidge, Clive A Miesel, Lynn Sweeney, Deb Shinabarger, Dean L Boulos, Ramiz A Preclinical development of Ramizol, an antibiotic belonging to a new class, for the treatment of Clostridium difficile colitis |
title | Preclinical development of Ramizol, an antibiotic belonging to a new class, for the treatment of Clostridium difficile colitis |
title_full | Preclinical development of Ramizol, an antibiotic belonging to a new class, for the treatment of Clostridium difficile colitis |
title_fullStr | Preclinical development of Ramizol, an antibiotic belonging to a new class, for the treatment of Clostridium difficile colitis |
title_full_unstemmed | Preclinical development of Ramizol, an antibiotic belonging to a new class, for the treatment of Clostridium difficile colitis |
title_short | Preclinical development of Ramizol, an antibiotic belonging to a new class, for the treatment of Clostridium difficile colitis |
title_sort | preclinical development of ramizol, an antibiotic belonging to a new class, for the treatment of clostridium difficile colitis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399159/ https://www.ncbi.nlm.nih.gov/pubmed/27189122 http://dx.doi.org/10.1038/ja.2016.45 |
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