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A simple and predictive phenotypic High Content Imaging assay for Plasmodium falciparum mature gametocytes to identify malaria transmission blocking compounds

Plasmodium falciparum gametocytes, specifically the mature stages, are the only malaria parasite stage in humans transmissible to the mosquito vector. Anti-malarial drugs capable of killing these forms are considered essential for the eradication of malaria and tools allowing the screening of large...

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Autores principales: Lucantoni, Leonardo, Silvestrini, Francesco, Signore, Michele, Siciliano, Giulia, Eldering, Maarten, Dechering, Koen J., Avery, Vicky M., Alano, Pietro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4639769/
https://www.ncbi.nlm.nih.gov/pubmed/26553647
http://dx.doi.org/10.1038/srep16414
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author Lucantoni, Leonardo
Silvestrini, Francesco
Signore, Michele
Siciliano, Giulia
Eldering, Maarten
Dechering, Koen J.
Avery, Vicky M.
Alano, Pietro
author_facet Lucantoni, Leonardo
Silvestrini, Francesco
Signore, Michele
Siciliano, Giulia
Eldering, Maarten
Dechering, Koen J.
Avery, Vicky M.
Alano, Pietro
author_sort Lucantoni, Leonardo
collection PubMed
description Plasmodium falciparum gametocytes, specifically the mature stages, are the only malaria parasite stage in humans transmissible to the mosquito vector. Anti-malarial drugs capable of killing these forms are considered essential for the eradication of malaria and tools allowing the screening of large compound libraries with high predictive power are needed to identify new candidates. As gametocytes are not a replicative stage it is difficult to apply the same drug screening methods used for asexual stages. Here we propose an assay, based on high content imaging, combining “classic” gametocyte viability readout based on gametocyte counts with a functional viability readout, based on gametocyte activation and the discrimination of the typical gamete spherical morphology. This simple and rapid assay has been miniaturized to a 384-well format using acridine orange staining of wild type P. falciparum 3D7A sexual forms, and was validated by screening reference antimalarial drugs and the MMV Malaria Box. The assay demonstrated excellent robustness and ability to identify quality hits with high likelihood of confirmation of transmission reducing activity in subsequent mosquito membrane feeding assays.
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spelling pubmed-46397692015-11-16 A simple and predictive phenotypic High Content Imaging assay for Plasmodium falciparum mature gametocytes to identify malaria transmission blocking compounds Lucantoni, Leonardo Silvestrini, Francesco Signore, Michele Siciliano, Giulia Eldering, Maarten Dechering, Koen J. Avery, Vicky M. Alano, Pietro Sci Rep Article Plasmodium falciparum gametocytes, specifically the mature stages, are the only malaria parasite stage in humans transmissible to the mosquito vector. Anti-malarial drugs capable of killing these forms are considered essential for the eradication of malaria and tools allowing the screening of large compound libraries with high predictive power are needed to identify new candidates. As gametocytes are not a replicative stage it is difficult to apply the same drug screening methods used for asexual stages. Here we propose an assay, based on high content imaging, combining “classic” gametocyte viability readout based on gametocyte counts with a functional viability readout, based on gametocyte activation and the discrimination of the typical gamete spherical morphology. This simple and rapid assay has been miniaturized to a 384-well format using acridine orange staining of wild type P. falciparum 3D7A sexual forms, and was validated by screening reference antimalarial drugs and the MMV Malaria Box. The assay demonstrated excellent robustness and ability to identify quality hits with high likelihood of confirmation of transmission reducing activity in subsequent mosquito membrane feeding assays. Nature Publishing Group 2015-11-10 /pmc/articles/PMC4639769/ /pubmed/26553647 http://dx.doi.org/10.1038/srep16414 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 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/4.0/
spellingShingle Article
Lucantoni, Leonardo
Silvestrini, Francesco
Signore, Michele
Siciliano, Giulia
Eldering, Maarten
Dechering, Koen J.
Avery, Vicky M.
Alano, Pietro
A simple and predictive phenotypic High Content Imaging assay for Plasmodium falciparum mature gametocytes to identify malaria transmission blocking compounds
title A simple and predictive phenotypic High Content Imaging assay for Plasmodium falciparum mature gametocytes to identify malaria transmission blocking compounds
title_full A simple and predictive phenotypic High Content Imaging assay for Plasmodium falciparum mature gametocytes to identify malaria transmission blocking compounds
title_fullStr A simple and predictive phenotypic High Content Imaging assay for Plasmodium falciparum mature gametocytes to identify malaria transmission blocking compounds
title_full_unstemmed A simple and predictive phenotypic High Content Imaging assay for Plasmodium falciparum mature gametocytes to identify malaria transmission blocking compounds
title_short A simple and predictive phenotypic High Content Imaging assay for Plasmodium falciparum mature gametocytes to identify malaria transmission blocking compounds
title_sort simple and predictive phenotypic high content imaging assay for plasmodium falciparum mature gametocytes to identify malaria transmission blocking compounds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4639769/
https://www.ncbi.nlm.nih.gov/pubmed/26553647
http://dx.doi.org/10.1038/srep16414
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