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Evaluation of the Anti-Leishmanial Effect of Recombinant Clostridium α-Toxin
BACKGROUND: Leishmaniasis is an infectious disease common in tropical and subtropical regions caused by the genus Leishmania, which is transmitted by the bite of female sandflies. In this study, we evaluate the anti-leishmanial effect of recombinant Clostridium α-toxin protein alone and the combinat...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7369417/ https://www.ncbi.nlm.nih.gov/pubmed/32765010 http://dx.doi.org/10.2147/IDR.S257561 |
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author | Namdar, Fatemeh Khanahmad, Hossein Ghayour, Zahra Mirzaei, Farzaneh Namdar, Azam Aghaei, Maryam Izadi, Shahrokh Khamesipour, Faham Hejazi, Seyed Hossein |
author_facet | Namdar, Fatemeh Khanahmad, Hossein Ghayour, Zahra Mirzaei, Farzaneh Namdar, Azam Aghaei, Maryam Izadi, Shahrokh Khamesipour, Faham Hejazi, Seyed Hossein |
author_sort | Namdar, Fatemeh |
collection | PubMed |
description | BACKGROUND: Leishmaniasis is an infectious disease common in tropical and subtropical regions caused by the genus Leishmania, which is transmitted by the bite of female sandflies. In this study, we evaluate the anti-leishmanial effect of recombinant Clostridium α-toxin protein alone and the combination with glucantime through in vitro and in vivo. MATERIALS AND METHODS: Production, expression, and purification of recombinant α-toxin were evaluated by SDS-PAGE and Western blotting techniques. The antileishmanial activities of the purified α-toxin plus and without glucantime were examined in vitro and in vivo. RESULTS: The results indicated successful expression of α-toxin as a 48 kDa band on SDS-PAGE and Western blot methods. Also, evaluation of α-toxin IC(50) showed the strong fatal effect of it, and glucantime on medium proliferated Leishmania promastigotes at lower concentrations compared with glucantime or α-toxin alone. Moreover, in vivo surveys showed that at the end of treatment courses, the mean of lesion size diminished in glucantime plus α-toxin treated mice versus negative control groups (p < 0.001). Also, there was a significant difference in the parasite burden of the spleen and liver of the control versus the test groups (p < 0.001). CONCLUSION: The results showed recombinant α-toxin has synergistic effects with glucantime in destroying Leishmania parasites. |
format | Online Article Text |
id | pubmed-7369417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-73694172020-08-05 Evaluation of the Anti-Leishmanial Effect of Recombinant Clostridium α-Toxin Namdar, Fatemeh Khanahmad, Hossein Ghayour, Zahra Mirzaei, Farzaneh Namdar, Azam Aghaei, Maryam Izadi, Shahrokh Khamesipour, Faham Hejazi, Seyed Hossein Infect Drug Resist Original Research BACKGROUND: Leishmaniasis is an infectious disease common in tropical and subtropical regions caused by the genus Leishmania, which is transmitted by the bite of female sandflies. In this study, we evaluate the anti-leishmanial effect of recombinant Clostridium α-toxin protein alone and the combination with glucantime through in vitro and in vivo. MATERIALS AND METHODS: Production, expression, and purification of recombinant α-toxin were evaluated by SDS-PAGE and Western blotting techniques. The antileishmanial activities of the purified α-toxin plus and without glucantime were examined in vitro and in vivo. RESULTS: The results indicated successful expression of α-toxin as a 48 kDa band on SDS-PAGE and Western blot methods. Also, evaluation of α-toxin IC(50) showed the strong fatal effect of it, and glucantime on medium proliferated Leishmania promastigotes at lower concentrations compared with glucantime or α-toxin alone. Moreover, in vivo surveys showed that at the end of treatment courses, the mean of lesion size diminished in glucantime plus α-toxin treated mice versus negative control groups (p < 0.001). Also, there was a significant difference in the parasite burden of the spleen and liver of the control versus the test groups (p < 0.001). CONCLUSION: The results showed recombinant α-toxin has synergistic effects with glucantime in destroying Leishmania parasites. Dove 2020-07-15 /pmc/articles/PMC7369417/ /pubmed/32765010 http://dx.doi.org/10.2147/IDR.S257561 Text en © 2020 Namdar et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Namdar, Fatemeh Khanahmad, Hossein Ghayour, Zahra Mirzaei, Farzaneh Namdar, Azam Aghaei, Maryam Izadi, Shahrokh Khamesipour, Faham Hejazi, Seyed Hossein Evaluation of the Anti-Leishmanial Effect of Recombinant Clostridium α-Toxin |
title | Evaluation of the Anti-Leishmanial Effect of Recombinant Clostridium α-Toxin |
title_full | Evaluation of the Anti-Leishmanial Effect of Recombinant Clostridium α-Toxin |
title_fullStr | Evaluation of the Anti-Leishmanial Effect of Recombinant Clostridium α-Toxin |
title_full_unstemmed | Evaluation of the Anti-Leishmanial Effect of Recombinant Clostridium α-Toxin |
title_short | Evaluation of the Anti-Leishmanial Effect of Recombinant Clostridium α-Toxin |
title_sort | evaluation of the anti-leishmanial effect of recombinant clostridium α-toxin |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7369417/ https://www.ncbi.nlm.nih.gov/pubmed/32765010 http://dx.doi.org/10.2147/IDR.S257561 |
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