Evidence map›Paper›PMID 42304683›Full record

ArticleThe Journal of infectious diseases2026

Characterizing the Circulation of Gametocytes and Mosquito Infectivity in Induced Blood Stage Malaria.

Louise Marquart-Wilson, Manon Alkema, Katharine A Collins, Kjerstin Lanke, Peter O'Rourke, Stacey Llewellyn, Lachlan Webb, Bridget E Barber, Teun Bousema, James S McCarthy

Abstract read
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Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Louise Marquart-WilsonSchool of Public Health, University of Queensland, Brisbane, Queensland,Australia.ORCID 0000-0003-4607-9060
Manon AlkemaDepartment of Medical Microbiology, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0002-8906-0047
Katharine A CollinsInfection and Inflammation Program, QIMR Berghofer, Brisbane, Queensland, Australia.
Kjerstin LankeDepartment of Medical Microbiology, Radboud University Medical Center, Nijmegen, The Netherlands.
Peter O'RourkeInfection and Inflammation Program, QIMR Berghofer, Brisbane, Queensland, Australia.
Stacey LlewellynPopulation Health Program, QIMR Berghofer, Brisbane, Queensland, Australia.ORCID 0000-0002-0564-947X
Lachlan WebbPopulation Health Program, QIMR Berghofer, Brisbane, Queensland, Australia.ORCID 0000-0002-5209-0314
Bridget E BarberInfection and Inflammation Program, QIMR Berghofer, Brisbane, Queensland, Australia.ORCID 0000-0003-1066-7960
Teun BousemaDepartment of Medical Microbiology, Radboud University Medical Center, Nijmegen, The Netherlands.
James S McCarthyInfection and Inflammation Program, QIMR Berghofer, Brisbane, Queensland, Australia.ORCID 0000-0001-6596-9718

Funding

European Research Council ERC-2014-StG 639776Gates FoundationGlobal Health Innovation and TechnologyNational Health and Medical Research Council 2016396National Health and Medical Research Council OPP1108403The Netherlands Organisation for Scientific Research 09150182210039Wellcome TrustWellcome Trust 095909/Z/11/Z
6 · The paper itself

Abstract

backgroundUnderstanding the influence of gametocyte dynamics on transmission of Plasmodium falciparum from humans to mosquitoes may support malaria elimination initiatives.

methodsLongitudinal parasitemia, gametocytemia, and mosquito transmission data from 91 participants in 9 controlled human malaria infection studies conducted in Brisbane, Australia (n = 8) and Nijmegen, the Netherlands (n = 1) were analyzed to explore the relationship of parasite and participant characteristics on gametocytes and transmission. Transmission potential estimated using Poisson probabilities was compared to transmission to Anopheles stephensi mosquitoes assessed using direct and membrane feeding assays across 5 clinical trials and 30 participants.

resultsMaximum gametocyte density over time per participant was positively correlated with asexual parasitemia at time of first treatment (ρ minimum = 0.44, maximum = 0.89). Median maximum gametocyte densities occurring 19-21 days postinoculation were 1087 gametocytes/mL for female and 219 gametocytes/mL for male gametocytes. Both female and male gametocyte densities were higher among individuals who infected mosquitoes, as were pretreatment parasite growth rates and parasite densities. Infectivity rates varied between 53% and 54% for direct skin, 29% and 33% for direct membrane, 54% and 100% for membrane after serum replacement, and 89% and 100% for enriched membrane feeding assays. Potential for transmission was correctly predicted for 71%-74% of direct feeding assays and 50%-78% of membrane after serum replacement feeding assays.

conclusionsThis study confirms that transmissible gametocyte densities can be consistently achieved in controlled infections. Higher asexual densities and growth rates were associated with higher gametocyte densities and higher transmission. Detailed understanding of how low-level gametocytemia contributes to transmission will guide both experimental infection studies and interventions to interrupt transmission.

Indexed as

AnophelesMalaria, FalciparumMosquito VectorsPlasmodium falciparumAdultAnimalsAustraliaFemaleHumansLongitudinal StudiesMaleNetherlandsParasitemiagametocytesinduced blood stage malariamosquito infectivityPlasmodium falciparumtransmission

Identifiers

PMID42304683
PMCPMC13668359

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.