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High-Throughput Assay and Discovery of Small Molecules that Interrupt Malaria Transmission
Preventing transmission is an important element of malaria control. However, most of the current available methods to assay for malaria transmission blocking are relatively low throughput and cannot be applied to large chemical libraries. We have developed a high-throughput and cost-effective assay,...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4723716/ https://www.ncbi.nlm.nih.gov/pubmed/26749441 http://dx.doi.org/10.1016/j.chom.2015.12.001 |
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author | Plouffe, David M. Wree, Melanie Du, Alan Y. Meister, Stephan Li, Fengwu Patra, Kailash Lubar, Aristea Okitsu, Shinji L. Flannery, Erika L. Kato, Nobutaka Tanaseichuk, Olga Comer, Eamon Zhou, Bin Kuhen, Kelli Zhou, Yingyao Leroy, Didier Schreiber, Stuart L. Scherer, Christina A. Vinetz, Joseph Winzeler, Elizabeth A. |
author_facet | Plouffe, David M. Wree, Melanie Du, Alan Y. Meister, Stephan Li, Fengwu Patra, Kailash Lubar, Aristea Okitsu, Shinji L. Flannery, Erika L. Kato, Nobutaka Tanaseichuk, Olga Comer, Eamon Zhou, Bin Kuhen, Kelli Zhou, Yingyao Leroy, Didier Schreiber, Stuart L. Scherer, Christina A. Vinetz, Joseph Winzeler, Elizabeth A. |
author_sort | Plouffe, David M. |
collection | PubMed |
description | Preventing transmission is an important element of malaria control. However, most of the current available methods to assay for malaria transmission blocking are relatively low throughput and cannot be applied to large chemical libraries. We have developed a high-throughput and cost-effective assay, the Saponin-lysis Sexual Stage Assay (SaLSSA), for identifying small molecules with transmission-blocking capacity. SaLSSA analysis of 13,983 unique compounds uncovered that >90% of well-characterized antimalarials, including endoperoxides and 4-aminoquinolines, as well as compounds active against asexual blood stages, lost most of their killing activity when parasites developed into metabolically quiescent stage V gametocytes. On the other hand, we identified compounds with consistent low nanomolar transmission-blocking activity, some of which showed cross-reactivity against asexual blood and liver stages. The data clearly emphasize substantial physiological differences between sexual and asexual parasites and provide a tool and starting points for the discovery and development of transmission-blocking drugs. |
format | Online Article Text |
id | pubmed-4723716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47237162016-02-18 High-Throughput Assay and Discovery of Small Molecules that Interrupt Malaria Transmission Plouffe, David M. Wree, Melanie Du, Alan Y. Meister, Stephan Li, Fengwu Patra, Kailash Lubar, Aristea Okitsu, Shinji L. Flannery, Erika L. Kato, Nobutaka Tanaseichuk, Olga Comer, Eamon Zhou, Bin Kuhen, Kelli Zhou, Yingyao Leroy, Didier Schreiber, Stuart L. Scherer, Christina A. Vinetz, Joseph Winzeler, Elizabeth A. Cell Host Microbe Resource Preventing transmission is an important element of malaria control. However, most of the current available methods to assay for malaria transmission blocking are relatively low throughput and cannot be applied to large chemical libraries. We have developed a high-throughput and cost-effective assay, the Saponin-lysis Sexual Stage Assay (SaLSSA), for identifying small molecules with transmission-blocking capacity. SaLSSA analysis of 13,983 unique compounds uncovered that >90% of well-characterized antimalarials, including endoperoxides and 4-aminoquinolines, as well as compounds active against asexual blood stages, lost most of their killing activity when parasites developed into metabolically quiescent stage V gametocytes. On the other hand, we identified compounds with consistent low nanomolar transmission-blocking activity, some of which showed cross-reactivity against asexual blood and liver stages. The data clearly emphasize substantial physiological differences between sexual and asexual parasites and provide a tool and starting points for the discovery and development of transmission-blocking drugs. Cell Press 2016-01-13 /pmc/articles/PMC4723716/ /pubmed/26749441 http://dx.doi.org/10.1016/j.chom.2015.12.001 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Resource Plouffe, David M. Wree, Melanie Du, Alan Y. Meister, Stephan Li, Fengwu Patra, Kailash Lubar, Aristea Okitsu, Shinji L. Flannery, Erika L. Kato, Nobutaka Tanaseichuk, Olga Comer, Eamon Zhou, Bin Kuhen, Kelli Zhou, Yingyao Leroy, Didier Schreiber, Stuart L. Scherer, Christina A. Vinetz, Joseph Winzeler, Elizabeth A. High-Throughput Assay and Discovery of Small Molecules that Interrupt Malaria Transmission |
title | High-Throughput Assay and Discovery of Small Molecules that Interrupt Malaria Transmission |
title_full | High-Throughput Assay and Discovery of Small Molecules that Interrupt Malaria Transmission |
title_fullStr | High-Throughput Assay and Discovery of Small Molecules that Interrupt Malaria Transmission |
title_full_unstemmed | High-Throughput Assay and Discovery of Small Molecules that Interrupt Malaria Transmission |
title_short | High-Throughput Assay and Discovery of Small Molecules that Interrupt Malaria Transmission |
title_sort | high-throughput assay and discovery of small molecules that interrupt malaria transmission |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4723716/ https://www.ncbi.nlm.nih.gov/pubmed/26749441 http://dx.doi.org/10.1016/j.chom.2015.12.001 |
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