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Rapid and Specific Action of Methylene Blue against Plasmodium Transmission Stages

Methylene blue (MB) is the oldest synthetic anti-infective. Its high potency against asexual and sexual stages of malaria parasites is well documented. This study aimed to investigate possible additional activities of MB in interfering with parasite transmission and determine target stages in Anophe...

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Autores principales: Saison, Nathanaël, Franetich, Jean-François, Pinilla, Yudi T., Hoffmann, Anton, Boussougou-Sambe, Stravensky T., Ngossanga, Barclaye, Tefit, Maurel, Ashraf, Kutub, Amanzougaghene, Nadia, Tajeri, Shahin, Adegnika, Ayola A., Mazier, Dominique, Borrmann, Steffen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9786052/
https://www.ncbi.nlm.nih.gov/pubmed/36559287
http://dx.doi.org/10.3390/pharmaceutics14122794
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author Saison, Nathanaël
Franetich, Jean-François
Pinilla, Yudi T.
Hoffmann, Anton
Boussougou-Sambe, Stravensky T.
Ngossanga, Barclaye
Tefit, Maurel
Ashraf, Kutub
Amanzougaghene, Nadia
Tajeri, Shahin
Adegnika, Ayola A.
Mazier, Dominique
Borrmann, Steffen
author_facet Saison, Nathanaël
Franetich, Jean-François
Pinilla, Yudi T.
Hoffmann, Anton
Boussougou-Sambe, Stravensky T.
Ngossanga, Barclaye
Tefit, Maurel
Ashraf, Kutub
Amanzougaghene, Nadia
Tajeri, Shahin
Adegnika, Ayola A.
Mazier, Dominique
Borrmann, Steffen
author_sort Saison, Nathanaël
collection PubMed
description Methylene blue (MB) is the oldest synthetic anti-infective. Its high potency against asexual and sexual stages of malaria parasites is well documented. This study aimed to investigate possible additional activities of MB in interfering with parasite transmission and determine target stages in Anopheles vectors and humans. MB’s transmission-blocking activity was first evaluated by an ex vivo direct membrane feeding assay (DMFA) using Plasmodium falciparum field isolates. To investigate anti-mosquito stage activity, Plasmodium berghei-infected Anopheles stephensi mosquitoes were fed a second blood meal on mice that had been treated with methylene blue, 3, 6- and 15-days after the initial infectious blood meal. Anti-sporozoite and liver stage activities were evaluated in vitro and in vivo via sporozoite invasion and liver stage development assays, respectively. MB exhibited a robust inhibition of P. falciparum transmission in An. gambiae, even when added shortly before the DMFA but only a moderate effect against P. berghei oocyst development. Exposure of mature P. berghei and P. falciparum sporozoites to MB blocked hepatocyte invasion, yet P. berghei liver stage development was unaffected by MB. Our results indicate previously underappreciated rapid specific activities of methylene blue against Plasmodium transmission stages, preventing the establishment of both mosquito midgut and liver infections as the first essential steps in both hosts.
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spelling pubmed-97860522022-12-24 Rapid and Specific Action of Methylene Blue against Plasmodium Transmission Stages Saison, Nathanaël Franetich, Jean-François Pinilla, Yudi T. Hoffmann, Anton Boussougou-Sambe, Stravensky T. Ngossanga, Barclaye Tefit, Maurel Ashraf, Kutub Amanzougaghene, Nadia Tajeri, Shahin Adegnika, Ayola A. Mazier, Dominique Borrmann, Steffen Pharmaceutics Article Methylene blue (MB) is the oldest synthetic anti-infective. Its high potency against asexual and sexual stages of malaria parasites is well documented. This study aimed to investigate possible additional activities of MB in interfering with parasite transmission and determine target stages in Anopheles vectors and humans. MB’s transmission-blocking activity was first evaluated by an ex vivo direct membrane feeding assay (DMFA) using Plasmodium falciparum field isolates. To investigate anti-mosquito stage activity, Plasmodium berghei-infected Anopheles stephensi mosquitoes were fed a second blood meal on mice that had been treated with methylene blue, 3, 6- and 15-days after the initial infectious blood meal. Anti-sporozoite and liver stage activities were evaluated in vitro and in vivo via sporozoite invasion and liver stage development assays, respectively. MB exhibited a robust inhibition of P. falciparum transmission in An. gambiae, even when added shortly before the DMFA but only a moderate effect against P. berghei oocyst development. Exposure of mature P. berghei and P. falciparum sporozoites to MB blocked hepatocyte invasion, yet P. berghei liver stage development was unaffected by MB. Our results indicate previously underappreciated rapid specific activities of methylene blue against Plasmodium transmission stages, preventing the establishment of both mosquito midgut and liver infections as the first essential steps in both hosts. MDPI 2022-12-14 /pmc/articles/PMC9786052/ /pubmed/36559287 http://dx.doi.org/10.3390/pharmaceutics14122794 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Saison, Nathanaël
Franetich, Jean-François
Pinilla, Yudi T.
Hoffmann, Anton
Boussougou-Sambe, Stravensky T.
Ngossanga, Barclaye
Tefit, Maurel
Ashraf, Kutub
Amanzougaghene, Nadia
Tajeri, Shahin
Adegnika, Ayola A.
Mazier, Dominique
Borrmann, Steffen
Rapid and Specific Action of Methylene Blue against Plasmodium Transmission Stages
title Rapid and Specific Action of Methylene Blue against Plasmodium Transmission Stages
title_full Rapid and Specific Action of Methylene Blue against Plasmodium Transmission Stages
title_fullStr Rapid and Specific Action of Methylene Blue against Plasmodium Transmission Stages
title_full_unstemmed Rapid and Specific Action of Methylene Blue against Plasmodium Transmission Stages
title_short Rapid and Specific Action of Methylene Blue against Plasmodium Transmission Stages
title_sort rapid and specific action of methylene blue against plasmodium transmission stages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9786052/
https://www.ncbi.nlm.nih.gov/pubmed/36559287
http://dx.doi.org/10.3390/pharmaceutics14122794
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