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Activity of Chitosan and Its Derivatives against Leishmania major and Leishmania mexicana In Vitro
There is an urgent need for safe, efficacious, affordable, and field-adapted drugs for the treatment of cutaneous leishmaniasis, which newly affects around 1.5 million people worldwide annually. Chitosan, a biodegradable cationic polysaccharide, has previously been reported to have antimicrobial, an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038302/ https://www.ncbi.nlm.nih.gov/pubmed/31871082 http://dx.doi.org/10.1128/AAC.01772-19 |
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author | Riezk, Alaa Raynes, John G. Yardley, Vanessa Murdan, Sudaxshina Croft, Simon L. |
author_facet | Riezk, Alaa Raynes, John G. Yardley, Vanessa Murdan, Sudaxshina Croft, Simon L. |
author_sort | Riezk, Alaa |
collection | PubMed |
description | There is an urgent need for safe, efficacious, affordable, and field-adapted drugs for the treatment of cutaneous leishmaniasis, which newly affects around 1.5 million people worldwide annually. Chitosan, a biodegradable cationic polysaccharide, has previously been reported to have antimicrobial, antileishmanial, and immunostimulatory activities. We investigated the in vitro activity of chitosan and several of its derivatives and showed that the pH of the culture medium plays a critical role in antileishmanial activity of chitosan against both extracellular promastigotes and intracellular amastigotes of Leishmania major and Leishmania mexicana. Chitosan and its derivatives were approximately 7 to 20 times more active at pH 6.5 than at pH 7.5, with high-molecular-weight chitosan being the most potent. High-molecular-weight chitosan stimulated the production of nitric oxide and reactive oxygen species by uninfected and Leishmania-infected macrophages in a time- and dose-dependent manner at pH 6.5. Despite the in vitro activation of bone marrow macrophages by chitosan to produce nitric oxide and reactive oxygen species, we showed that the antileishmanial activity of chitosan was not mediated by these metabolites. Finally, we showed that rhodamine-labeled chitosan is taken up by pinocytosis and accumulates in the parasitophorous vacuole of Leishmania-infected macrophages. |
format | Online Article Text |
id | pubmed-7038302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-70383022020-03-06 Activity of Chitosan and Its Derivatives against Leishmania major and Leishmania mexicana In Vitro Riezk, Alaa Raynes, John G. Yardley, Vanessa Murdan, Sudaxshina Croft, Simon L. Antimicrob Agents Chemother Experimental Therapeutics There is an urgent need for safe, efficacious, affordable, and field-adapted drugs for the treatment of cutaneous leishmaniasis, which newly affects around 1.5 million people worldwide annually. Chitosan, a biodegradable cationic polysaccharide, has previously been reported to have antimicrobial, antileishmanial, and immunostimulatory activities. We investigated the in vitro activity of chitosan and several of its derivatives and showed that the pH of the culture medium plays a critical role in antileishmanial activity of chitosan against both extracellular promastigotes and intracellular amastigotes of Leishmania major and Leishmania mexicana. Chitosan and its derivatives were approximately 7 to 20 times more active at pH 6.5 than at pH 7.5, with high-molecular-weight chitosan being the most potent. High-molecular-weight chitosan stimulated the production of nitric oxide and reactive oxygen species by uninfected and Leishmania-infected macrophages in a time- and dose-dependent manner at pH 6.5. Despite the in vitro activation of bone marrow macrophages by chitosan to produce nitric oxide and reactive oxygen species, we showed that the antileishmanial activity of chitosan was not mediated by these metabolites. Finally, we showed that rhodamine-labeled chitosan is taken up by pinocytosis and accumulates in the parasitophorous vacuole of Leishmania-infected macrophages. American Society for Microbiology 2020-02-21 /pmc/articles/PMC7038302/ /pubmed/31871082 http://dx.doi.org/10.1128/AAC.01772-19 Text en Copyright © 2020 Riezk et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Experimental Therapeutics Riezk, Alaa Raynes, John G. Yardley, Vanessa Murdan, Sudaxshina Croft, Simon L. Activity of Chitosan and Its Derivatives against Leishmania major and Leishmania mexicana In Vitro |
title | Activity of Chitosan and Its Derivatives against Leishmania major and Leishmania mexicana
In Vitro |
title_full | Activity of Chitosan and Its Derivatives against Leishmania major and Leishmania mexicana
In Vitro |
title_fullStr | Activity of Chitosan and Its Derivatives against Leishmania major and Leishmania mexicana
In Vitro |
title_full_unstemmed | Activity of Chitosan and Its Derivatives against Leishmania major and Leishmania mexicana
In Vitro |
title_short | Activity of Chitosan and Its Derivatives against Leishmania major and Leishmania mexicana
In Vitro |
title_sort | activity of chitosan and its derivatives against leishmania major and leishmania mexicana
in vitro |
topic | Experimental Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038302/ https://www.ncbi.nlm.nih.gov/pubmed/31871082 http://dx.doi.org/10.1128/AAC.01772-19 |
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