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

dc.contributor.authorKazutoyo Miuraen_US
dc.contributor.authorBruce J. Swiharten_US
dc.contributor.authorMichael P. Fayen_US
dc.contributor.authorChalermpon Kumpitaken_US
dc.contributor.authorKirakorn Kiattibutren_US
dc.contributor.authorJetsumon Sattabongkoten_US
dc.contributor.authorCarole A. Longen_US
dc.contributor.otherNational Institute of Allergy and Infectious Diseases (NIAID)en_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2020-08-25T12:00:44Z
dc.date.available2020-08-25T12:00:44Z
dc.date.issued2020-12-01en_US
dc.description.abstract© 2020, The Author(s). 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.en_US
dc.identifier.citationScientific Reports. Vol.10, No.1 (2020)en_US
dc.identifier.doi10.1038/s41598-020-69513-xen_US
dc.identifier.issn20452322en_US
dc.identifier.other2-s2.0-85088654147en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/58394
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85088654147&origin=inwarden_US
dc.subjectMultidisciplinaryen_US
dc.titleEvaluation and modeling of direct membrane-feeding assay with Plasmodium vivax to support development of transmission blocking vaccinesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85088654147&origin=inwarden_US

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