Cargando…

The Activities of Current Antimalarial Drugs on the Life Cycle Stages of Plasmodium: A Comparative Study with Human and Rodent Parasites

BACKGROUND: Malaria remains a disease of devastating global impact, killing more than 800,000 people every year—the vast majority being children under the age of 5. While effective therapies are available, if malaria is to be eradicated a broader range of small molecule therapeutics that are able to...

Descripción completa

Detalles Bibliográficos
Autores principales: Delves, Michael, Plouffe, David, Scheurer, Christian, Meister, Stephan, Wittlin, Sergio, Winzeler, Elizabeth A., Sinden, Robert E., Leroy, Didier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283556/
https://www.ncbi.nlm.nih.gov/pubmed/22363211
http://dx.doi.org/10.1371/journal.pmed.1001169
_version_ 1782224209449058304
author Delves, Michael
Plouffe, David
Scheurer, Christian
Meister, Stephan
Wittlin, Sergio
Winzeler, Elizabeth A.
Sinden, Robert E.
Leroy, Didier
author_facet Delves, Michael
Plouffe, David
Scheurer, Christian
Meister, Stephan
Wittlin, Sergio
Winzeler, Elizabeth A.
Sinden, Robert E.
Leroy, Didier
author_sort Delves, Michael
collection PubMed
description BACKGROUND: Malaria remains a disease of devastating global impact, killing more than 800,000 people every year—the vast majority being children under the age of 5. While effective therapies are available, if malaria is to be eradicated a broader range of small molecule therapeutics that are able to target the liver and the transmissible sexual stages are required. These new medicines are needed both to meet the challenge of malaria eradication and to circumvent resistance. METHODS AND FINDINGS: Little is known about the wider stage-specific activities of current antimalarials that were primarily designed to alleviate symptoms of malaria in the blood stage. To overcome this critical gap, we developed assays to measure activity of antimalarials against all life stages of malaria parasites, using a diverse set of human and nonhuman parasite species, including male gamete production (exflagellation) in Plasmodium falciparum, ookinete development in P. berghei, oocyst development in P. berghei and P. falciparum, and the liver stage of P. yoelii. We then compared 50 current and experimental antimalarials in these assays. We show that endoperoxides such as OZ439, a stable synthetic molecule currently in clinical phase IIa trials, are strong inhibitors of gametocyte maturation/gamete formation and impact sporogony; lumefantrine impairs development in the vector; and NPC-1161B, a new 8-aminoquinoline, inhibits sporogony. CONCLUSIONS: These data enable objective comparisons of the strengths and weaknesses of each chemical class at targeting each stage of the lifecycle. Noting that the activities of many compounds lie within achievable blood concentrations, these results offer an invaluable guide to decisions regarding which drugs to combine in the next-generation of antimalarial drugs. This study might reveal the potential of life-cycle–wide analyses of drugs for other pathogens with complex life cycles. Please see later in the article for the Editors' Summary
format Online
Article
Text
id pubmed-3283556
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-32835562012-02-23 The Activities of Current Antimalarial Drugs on the Life Cycle Stages of Plasmodium: A Comparative Study with Human and Rodent Parasites Delves, Michael Plouffe, David Scheurer, Christian Meister, Stephan Wittlin, Sergio Winzeler, Elizabeth A. Sinden, Robert E. Leroy, Didier PLoS Med Research Article BACKGROUND: Malaria remains a disease of devastating global impact, killing more than 800,000 people every year—the vast majority being children under the age of 5. While effective therapies are available, if malaria is to be eradicated a broader range of small molecule therapeutics that are able to target the liver and the transmissible sexual stages are required. These new medicines are needed both to meet the challenge of malaria eradication and to circumvent resistance. METHODS AND FINDINGS: Little is known about the wider stage-specific activities of current antimalarials that were primarily designed to alleviate symptoms of malaria in the blood stage. To overcome this critical gap, we developed assays to measure activity of antimalarials against all life stages of malaria parasites, using a diverse set of human and nonhuman parasite species, including male gamete production (exflagellation) in Plasmodium falciparum, ookinete development in P. berghei, oocyst development in P. berghei and P. falciparum, and the liver stage of P. yoelii. We then compared 50 current and experimental antimalarials in these assays. We show that endoperoxides such as OZ439, a stable synthetic molecule currently in clinical phase IIa trials, are strong inhibitors of gametocyte maturation/gamete formation and impact sporogony; lumefantrine impairs development in the vector; and NPC-1161B, a new 8-aminoquinoline, inhibits sporogony. CONCLUSIONS: These data enable objective comparisons of the strengths and weaknesses of each chemical class at targeting each stage of the lifecycle. Noting that the activities of many compounds lie within achievable blood concentrations, these results offer an invaluable guide to decisions regarding which drugs to combine in the next-generation of antimalarial drugs. This study might reveal the potential of life-cycle–wide analyses of drugs for other pathogens with complex life cycles. Please see later in the article for the Editors' Summary Public Library of Science 2012-02-21 /pmc/articles/PMC3283556/ /pubmed/22363211 http://dx.doi.org/10.1371/journal.pmed.1001169 Text en Delves et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Delves, Michael
Plouffe, David
Scheurer, Christian
Meister, Stephan
Wittlin, Sergio
Winzeler, Elizabeth A.
Sinden, Robert E.
Leroy, Didier
The Activities of Current Antimalarial Drugs on the Life Cycle Stages of Plasmodium: A Comparative Study with Human and Rodent Parasites
title The Activities of Current Antimalarial Drugs on the Life Cycle Stages of Plasmodium: A Comparative Study with Human and Rodent Parasites
title_full The Activities of Current Antimalarial Drugs on the Life Cycle Stages of Plasmodium: A Comparative Study with Human and Rodent Parasites
title_fullStr The Activities of Current Antimalarial Drugs on the Life Cycle Stages of Plasmodium: A Comparative Study with Human and Rodent Parasites
title_full_unstemmed The Activities of Current Antimalarial Drugs on the Life Cycle Stages of Plasmodium: A Comparative Study with Human and Rodent Parasites
title_short The Activities of Current Antimalarial Drugs on the Life Cycle Stages of Plasmodium: A Comparative Study with Human and Rodent Parasites
title_sort activities of current antimalarial drugs on the life cycle stages of plasmodium: a comparative study with human and rodent parasites
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283556/
https://www.ncbi.nlm.nih.gov/pubmed/22363211
http://dx.doi.org/10.1371/journal.pmed.1001169
work_keys_str_mv AT delvesmichael theactivitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT plouffedavid theactivitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT scheurerchristian theactivitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT meisterstephan theactivitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT wittlinsergio theactivitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT winzelerelizabetha theactivitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT sindenroberte theactivitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT leroydidier theactivitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT delvesmichael activitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT plouffedavid activitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT scheurerchristian activitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT meisterstephan activitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT wittlinsergio activitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT winzelerelizabetha activitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT sindenroberte activitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites
AT leroydidier activitiesofcurrentantimalarialdrugsonthelifecyclestagesofplasmodiumacomparativestudywithhumanandrodentparasites