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Evaluation and modeling of direct membrane-feeding assay with Plasmodium vivax to support development of transmission blocking vaccines

Standard and direct membrane-feeding assays (SMFA and DMFA) are fundamental assays to evaluate efficacy of transmission-blocking intervention (TBI) candidates against Plasmodium falciparum and vivax. To compare different candidates precisely, it is crucial to understand the error range of measured a...

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Autores principales: Miura, Kazutoyo, Swihart, Bruce J., Fay, Michael P., Kumpitak, Chalermpon, Kiattibutr, Kirakorn, Sattabongkot, Jetsumon, Long, Carole A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387523/
https://www.ncbi.nlm.nih.gov/pubmed/32724063
http://dx.doi.org/10.1038/s41598-020-69513-x
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author Miura, Kazutoyo
Swihart, Bruce J.
Fay, Michael P.
Kumpitak, Chalermpon
Kiattibutr, Kirakorn
Sattabongkot, Jetsumon
Long, Carole A.
author_facet Miura, Kazutoyo
Swihart, Bruce J.
Fay, Michael P.
Kumpitak, Chalermpon
Kiattibutr, Kirakorn
Sattabongkot, Jetsumon
Long, Carole A.
author_sort Miura, Kazutoyo
collection PubMed
description Standard and direct membrane-feeding assays (SMFA and DMFA) are fundamental assays to evaluate efficacy of transmission-blocking intervention (TBI) candidates against Plasmodium falciparum and vivax. To compare different candidates precisely, it is crucial to understand the error range of measured activity, usually expressed as percent inhibition in either oocyst intensity (% transmission reducing activity, %TRA), or in prevalence of infected mosquitoes (% transmission blocking activity, %TBA). To this end, mathematical models have been proposed for P. falciparum SMFA (PfSMFA), but such study for DMFA is limited. In this study, we analyzed P. vivax DMFA (PvDMFA) data from 22,236 mosquitoes tested from 96 independent assays. While the two assays are quite different, a zero-inflated negative binomial (ZINB) model could reasonably explain the PvDMFA results, as it has for PfSMFA. Our simulation studies based on the ZINB model revealed it is better to report %TRA values with a proper error range, rather than observed %TBA both in SMFA and DMFA. Furthermore, the simulations help in designing a better assay and aid in estimating an error range of a %TRA value when the uncertainty is not reported. This study strongly supports future TBI development by providing a rational method to compare different candidates.
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spelling pubmed-73875232020-07-29 Evaluation and modeling of direct membrane-feeding assay with Plasmodium vivax to support development of transmission blocking vaccines Miura, Kazutoyo Swihart, Bruce J. Fay, Michael P. Kumpitak, Chalermpon Kiattibutr, Kirakorn Sattabongkot, Jetsumon Long, Carole A. Sci Rep Article Standard and direct membrane-feeding assays (SMFA and DMFA) are fundamental assays to evaluate efficacy of transmission-blocking intervention (TBI) candidates against Plasmodium falciparum and vivax. To compare different candidates precisely, it is crucial to understand the error range of measured activity, usually expressed as percent inhibition in either oocyst intensity (% transmission reducing activity, %TRA), or in prevalence of infected mosquitoes (% transmission blocking activity, %TBA). To this end, mathematical models have been proposed for P. falciparum SMFA (PfSMFA), but such study for DMFA is limited. In this study, we analyzed P. vivax DMFA (PvDMFA) data from 22,236 mosquitoes tested from 96 independent assays. While the two assays are quite different, a zero-inflated negative binomial (ZINB) model could reasonably explain the PvDMFA results, as it has for PfSMFA. Our simulation studies based on the ZINB model revealed it is better to report %TRA values with a proper error range, rather than observed %TBA both in SMFA and DMFA. Furthermore, the simulations help in designing a better assay and aid in estimating an error range of a %TRA value when the uncertainty is not reported. This study strongly supports future TBI development by providing a rational method to compare different candidates. Nature Publishing Group UK 2020-07-28 /pmc/articles/PMC7387523/ /pubmed/32724063 http://dx.doi.org/10.1038/s41598-020-69513-x Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2020 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Miura, Kazutoyo
Swihart, Bruce J.
Fay, Michael P.
Kumpitak, Chalermpon
Kiattibutr, Kirakorn
Sattabongkot, Jetsumon
Long, Carole A.
Evaluation and modeling of direct membrane-feeding assay with Plasmodium vivax to support development of transmission blocking vaccines
title Evaluation and modeling of direct membrane-feeding assay with Plasmodium vivax to support development of transmission blocking vaccines
title_full Evaluation and modeling of direct membrane-feeding assay with Plasmodium vivax to support development of transmission blocking vaccines
title_fullStr Evaluation and modeling of direct membrane-feeding assay with Plasmodium vivax to support development of transmission blocking vaccines
title_full_unstemmed Evaluation and modeling of direct membrane-feeding assay with Plasmodium vivax to support development of transmission blocking vaccines
title_short Evaluation and modeling of direct membrane-feeding assay with Plasmodium vivax to support development of transmission blocking vaccines
title_sort evaluation and modeling of direct membrane-feeding assay with plasmodium vivax to support development of transmission blocking vaccines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387523/
https://www.ncbi.nlm.nih.gov/pubmed/32724063
http://dx.doi.org/10.1038/s41598-020-69513-x
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