Evidence map›Paper›PMID 33903595›Full record

ArticleNature communications2021

Higher gametocyte production and mosquito infectivity in chronic compared to incident Plasmodium falciparum infections.

Aissata Barry, John Bradley, Will Stone, Moussa W Guelbeogo, Kjerstin Lanke, Alphonse Ouedraogo, Issiaka Soulama, Issa Nébié, Samuel S Serme, Lynn Grignard and 14 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
14.9field-weighted citation impact, top 1% of its field
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

60 citing papers in PubMed, 94 citations in OpenAlex.

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  8. Prevalence ofPathogens (Basel, Switzerland) · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors at 5 institutions in 4 countries.

Aissata Barry *Centre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou 01, Burkina Faso.
John Bradley *MRC International Statistics and Epidemiology Group, London School of Hygiene and Tropical Medicine, London, UK.ORCID 0000-0002-9449-4608
Will Stone *Department of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, UK.
Moussa W GuelbeogoCentre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou 01, Burkina Faso.
Kjerstin LankeRadboud Institute for Health Sciences and Radboud Center for Infectious Diseases, Radboud University Medical Centre, Nijmegen, The Netherlands.
Alphonse OuedraogoCentre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou 01, Burkina Faso.
Issiaka SoulamaCentre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou 01, Burkina Faso.ORCID 0000-0002-0993-0525
Issa NébiéCentre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou 01, Burkina Faso.
Samuel S SermeCentre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou 01, Burkina Faso.
Lynn GrignardDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, UK.ORCID 0000-0001-8305-3981
Catriona PattersonDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, UK.ORCID 0000-0002-4500-7199
Lindsey WuDepartment of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, UK.
Jessica J BriggsDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0002-8078-3898
Owen JansonDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA.
Shehu S AwanduRadboud Institute for Health Sciences and Radboud Center for Infectious Diseases, Radboud University Medical Centre, Nijmegen, The Netherlands.
Mireille OuedraogoCentre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou 01, Burkina Faso.
Casimire W TaramaCentre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou 01, Burkina Faso.ORCID 0000-0001-5228-7267
Désiré KargougouCentre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou 01, Burkina Faso.
Soumanaba ZongoCentre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou 01, Burkina Faso.
Sodiomon B SirimaCentre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou 01, Burkina Faso.
Matthias MartiWellcome Centre for Integrative Parasitology, University of Glasgow, Glasgow, UK.ORCID 0000-0003-1040-9566
Chris DrakeleyMRC International Statistics and Epidemiology Group, London School of Hygiene and Tropical Medicine, London, UK.ORCID 0000-0003-4863-075X
Alfred B TionoCentre National de Recherche et de Formation sur le Paludisme (CNRFP), Ouagadougou 01, Burkina Faso.
Teun BousemaRadboud Institute for Health Sciences and Radboud Center for Infectious Diseases, Radboud University Medical Centre, Nijmegen, The Netherlands. teun.bousema@radboudumc.nl.
Centre National de Recherche et de Formation sur le Paludisme · BFLondon School of Hygiene & Tropical Medicine · GBRadboud University Nijmegen · NLUniversity of California, San Francisco · USWellcome Centre for Molecular Parasitology · GB

Funding

Medical Research Council MR/R010161/1Wellcome TrustWellcome Trust 218676/Z/19/Z
6 · The paper itself

Abstract

Plasmodium falciparum gametocyte kinetics and infectivity may differ between chronic and incident infections. In the current study, we assess parasite kinetics and infectivity to mosquitoes among children (aged 5-10 years) from Burkina Faso with (a) incident infections following parasite clearance (n = 48) and (b) chronic asymptomatic infections (n = 60). In the incident infection cohort, 92% (44/48) of children develop symptoms within 35 days, compared to 23% (14/60) in the chronic cohort. All individuals with chronic infection carried gametocytes or developed them during follow-up, whereas only 35% (17/48) in the incident cohort produce gametocytes before becoming symptomatic and receiving treatment. Parasite multiplication rate (PMR) and the relative abundance of ap2-g and gexp-5 transcripts are positively associated with gametocyte production. Antibody responses are higher and PMR lower in chronic infections. The presence of symptoms and sexual stage immune responses are associated with reductions in gametocyte infectivity to mosquitoes. We observe that most incident infections require treatment before the density of mature gametocytes is sufficient to infect mosquitoes. In contrast, chronic, asymptomatic infections represent a significant source of mosquito infections. Our observations support the notion that malaria transmission reduction may be expedited by enhanced case management, involving both symptom-screening and infection detection.

Indexed as

AnimalsAnophelesBurkina FasoChildChild, PreschoolCohort StudiesFemaleHumansIncidenceInsect VectorsMalaria, FalciparumMalePlasmodium falciparumPopulation DensityTime Factors

Identifiers

PMID33903595
PMCPMC8076179
OpenAlexW3158066990

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.