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A Flow Cytometry-Based Quantitative Drug Sensitivity Assay for All Plasmodium falciparum Gametocyte Stages

BACKGROUND: Malaria elimination/eradication campaigns emphasize interruption of parasite transmission as a priority strategy. Screening for new drugs and vaccines against gametocytes is therefore urgently needed. However, current methods for sexual stage drug assays, usually performed by counting or...

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Autores principales: Wang, Zenglei, Liu, Min, Liang, Xiaoying, Siriwat, Salil, Li, Xiaolian, Chen, Xiaoguang, Parker, Daniel M., Miao, Jun, Cui, Liwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988044/
https://www.ncbi.nlm.nih.gov/pubmed/24736563
http://dx.doi.org/10.1371/journal.pone.0093825
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author Wang, Zenglei
Liu, Min
Liang, Xiaoying
Siriwat, Salil
Li, Xiaolian
Chen, Xiaoguang
Parker, Daniel M.
Miao, Jun
Cui, Liwang
author_facet Wang, Zenglei
Liu, Min
Liang, Xiaoying
Siriwat, Salil
Li, Xiaolian
Chen, Xiaoguang
Parker, Daniel M.
Miao, Jun
Cui, Liwang
author_sort Wang, Zenglei
collection PubMed
description BACKGROUND: Malaria elimination/eradication campaigns emphasize interruption of parasite transmission as a priority strategy. Screening for new drugs and vaccines against gametocytes is therefore urgently needed. However, current methods for sexual stage drug assays, usually performed by counting or via fluorescent markers are either laborious or restricted to a certain stage. Here we describe the use of a transgenic parasite line for assaying drug sensitivity in all gametocyte stages. METHODS: A transgenic parasite line expressing green fluorescence protein (GFP) under the control of the gametocyte-specific gene α-tubulin II promoter was generated. This parasite line expresses GFP in all gametocyte stages. Using this transgenic line, we developed a flow cytometry-based assay to determine drug sensitivity of all gametocyte stages, and tested the gametocytocidal activities of four antimalarial drugs. FINDINGS: This assay proved to be suitable for determining drug sensitivity of all sexual stages and can be automated. A Z’ factor of 0.79±0.02 indicated that this assay could be further optimized for high-throughput screening. The daily sensitivity of gametocytes to three antimalarial drugs (chloroquine, dihydroartemisinin and pyronaridine) showed a drastic decrease from stage III on, whereas it remained relatively steady for primaquine. CONCLUSIONS: A drug assay was developed to use a single transgenic parasite line for determining drug susceptibility of all gametocyte stages. This assay may be further automated into a high-throughput platform for screening compound libraries against P. falciparum gametocytes.
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spelling pubmed-39880442014-04-21 A Flow Cytometry-Based Quantitative Drug Sensitivity Assay for All Plasmodium falciparum Gametocyte Stages Wang, Zenglei Liu, Min Liang, Xiaoying Siriwat, Salil Li, Xiaolian Chen, Xiaoguang Parker, Daniel M. Miao, Jun Cui, Liwang PLoS One Research Article BACKGROUND: Malaria elimination/eradication campaigns emphasize interruption of parasite transmission as a priority strategy. Screening for new drugs and vaccines against gametocytes is therefore urgently needed. However, current methods for sexual stage drug assays, usually performed by counting or via fluorescent markers are either laborious or restricted to a certain stage. Here we describe the use of a transgenic parasite line for assaying drug sensitivity in all gametocyte stages. METHODS: A transgenic parasite line expressing green fluorescence protein (GFP) under the control of the gametocyte-specific gene α-tubulin II promoter was generated. This parasite line expresses GFP in all gametocyte stages. Using this transgenic line, we developed a flow cytometry-based assay to determine drug sensitivity of all gametocyte stages, and tested the gametocytocidal activities of four antimalarial drugs. FINDINGS: This assay proved to be suitable for determining drug sensitivity of all sexual stages and can be automated. A Z’ factor of 0.79±0.02 indicated that this assay could be further optimized for high-throughput screening. The daily sensitivity of gametocytes to three antimalarial drugs (chloroquine, dihydroartemisinin and pyronaridine) showed a drastic decrease from stage III on, whereas it remained relatively steady for primaquine. CONCLUSIONS: A drug assay was developed to use a single transgenic parasite line for determining drug susceptibility of all gametocyte stages. This assay may be further automated into a high-throughput platform for screening compound libraries against P. falciparum gametocytes. Public Library of Science 2014-04-15 /pmc/articles/PMC3988044/ /pubmed/24736563 http://dx.doi.org/10.1371/journal.pone.0093825 Text en © 2014 Wang 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
Wang, Zenglei
Liu, Min
Liang, Xiaoying
Siriwat, Salil
Li, Xiaolian
Chen, Xiaoguang
Parker, Daniel M.
Miao, Jun
Cui, Liwang
A Flow Cytometry-Based Quantitative Drug Sensitivity Assay for All Plasmodium falciparum Gametocyte Stages
title A Flow Cytometry-Based Quantitative Drug Sensitivity Assay for All Plasmodium falciparum Gametocyte Stages
title_full A Flow Cytometry-Based Quantitative Drug Sensitivity Assay for All Plasmodium falciparum Gametocyte Stages
title_fullStr A Flow Cytometry-Based Quantitative Drug Sensitivity Assay for All Plasmodium falciparum Gametocyte Stages
title_full_unstemmed A Flow Cytometry-Based Quantitative Drug Sensitivity Assay for All Plasmodium falciparum Gametocyte Stages
title_short A Flow Cytometry-Based Quantitative Drug Sensitivity Assay for All Plasmodium falciparum Gametocyte Stages
title_sort flow cytometry-based quantitative drug sensitivity assay for all plasmodium falciparum gametocyte stages
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3988044/
https://www.ncbi.nlm.nih.gov/pubmed/24736563
http://dx.doi.org/10.1371/journal.pone.0093825
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