Evidence map›Paper›PMID 37165325›Full record

ArticleBMC infectious diseases2023

Influence of the sickle cell trait on Plasmodium falciparum infectivity from naturally infected gametocyte carriers.

Christelle M Ngou, Albert N Bayibéki, Luc Abate, Olesula S Makinde, Lionel B Feufack-Donfack, Elangwe M Sarah-Matio, Aline G Bouopda-Tuedom, Paul Taconet, Nicolas Moiroux, Parfait H Awono-Ambéné and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Sickle Trait Hemoglobin Does Not Influence Anopheles Biting Rates.The American journal of tropical medicine and hygiene · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Sickle-trait hemoglobin does not influencemedRxiv : the preprint server for health sciences · 2025
    Article
  8. Human genetic variations conferring resistance to malaria.Journal of translational medicine · 2025
    Review
  9. Article
  10. Review
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

15 authors at 10 institutions in 4 countries.

Christelle M NgouInstitut de Recherche pour le Développement, MIVEGEC, Univ. Montpellier, CNRS, IRD, 91 Avenue Agropolis, BP 64501, 34394, Montpellier, France.
Albert N BayibékiUniversité Catholique d'Afrique Centrale, Yaoundé, Cameroon.
Luc AbateInstitut de Recherche pour le Développement, MIVEGEC, Univ. Montpellier, CNRS, IRD, 91 Avenue Agropolis, BP 64501, 34394, Montpellier, France.
Olesula S MakindeDepartment of Statistics, Federal University of Technology, P.M.B 704, Akure, Nigeria.
Lionel B Feufack-DonfackMalaria Research Unit, Centre Pasteur du Cameroun, Yaoundé, Cameroon.
Elangwe M Sarah-MatioInstitut de Recherche pour le Développement, MIVEGEC, Univ. Montpellier, CNRS, IRD, 91 Avenue Agropolis, BP 64501, 34394, Montpellier, France.
Aline G Bouopda-TuedomMalaria Research Unit, Centre Pasteur du Cameroun, Yaoundé, Cameroon.
Paul TaconetInstitut de Recherche pour le Développement, MIVEGEC, Univ. Montpellier, CNRS, IRD, 91 Avenue Agropolis, BP 64501, 34394, Montpellier, France.
Nicolas MoirouxInstitut de Recherche pour le Développement, MIVEGEC, Univ. Montpellier, CNRS, IRD, 91 Avenue Agropolis, BP 64501, 34394, Montpellier, France.
Parfait H Awono-AmbénéLaboratoire d'Entomologie Médicale, OCEAC, BP288, Yaoundé, Cameroon.
Arthur TalmanInstitut de Recherche pour le Développement, MIVEGEC, Univ. Montpellier, CNRS, IRD, 91 Avenue Agropolis, BP 64501, 34394, Montpellier, France.
Lawrence S AyongMalaria Research Unit, Centre Pasteur du Cameroun, Yaoundé, Cameroon.
Antoine BerryInstitut Toulousain des Maladies Infectieuses et Inflammatoires (Infinity), Université Toulouse, CNRS UMR5051, INSERM UMR1291, UPS, Toulouse, France.
Sandrine E Nsango *Malaria Research Unit, Centre Pasteur du Cameroun, Yaoundé, Cameroon.
Isabelle Morlais *Institut de Recherche pour le Développement, MIVEGEC, Univ. Montpellier, CNRS, IRD, 91 Avenue Agropolis, BP 64501, 34394, Montpellier, France. isabelle.morlais@ird.fr.
Centre National de la Recherche Scientifique · FRCentre Pasteur du Cameroun · CMMaladies Infectieuses et Vecteurs: Écologie, Génétique, Évolution et Contrôle · FRUniversité de Montpellier · FRUniversity of Douala · CMCatholic University of Central Africa · CMFederal University of Technology · NGInstitut de Recherche pour le Développement · FROrganisation de Coordination pour la lutte contre les Endémies en Afrique Centrale · CMUniversité Toulouse III - Paul Sabatier · FR

Funding

Département Soutien et Formation, Institut de Recherche pour le Développement ARTS programmeInstitut de Recherche pour le Développement JEAI IMPALA
6 · The paper itself

Abstract

backgroundSickle cell trait (SCT) refers to the carriage of one abnormal copy of the β-globin gene, the HbS allele. SCT offers protection against malaria, controlling parasite density and preventing progression to symptomatic malaria. However, it remains unclear whether SCT also affects transmission stages and mosquito infection parameters. Deciphering the impact of the SCT on human to mosquito malaria transmission is key to understanding mechanisms that maintain the trait in malaria endemic areas.

methodsThe study was conducted from June to July 2017 among asymptomatic children living in the locality of Mfou, Cameroon. Blood samples were collected from asymptomatic children to perform malaria diagnosis by microscopy, Plasmodium species by PCR and hemoglobin typing by RFLP. Infectiousness of gametocytes to mosquitoes was assessed by membrane feeding assays using blood from gametocyte carriers of HbAA and HbAS genotypes. A zero-inflated model was fitted to predict distribution of oocysts in mosquitoes according to hemoglobin genotype of the gametocyte source.

resultsAmong the 1557 children enrolled in the study, 314 (20.16%) were of the HbAS genotype. The prevalence of children with P. falciparum gametocytes was 18.47% in HbAS individuals and 13.57% in HbAA, and the difference is significant (χ

conclusionPlasmodium transmission stages were more prevalent in SCT individuals. This may reflect the parasite's enhanced investment in the sexual stage to increase their survival rate when asexual replication is impeded. The public health impact of our results points the need for intensive malaria control interventions in areas with high prevalence of HbAS. The similar infection parameters in feeding experiments where mosquitoes received the original serum from the blood donor indicated that immune responses to gametocyte surface proteins occur in both HbAS and HbAA individuals. The higher risk of infection in mosquitoes fed on HbAS blood depleted of immune factors suggests that changes in the membrane properties in HbAS erythrocytes may impact on the maturation process of gametocytes within circulating red blood cells.

Indexed as

AnophelesMalaria, FalciparumSickle Cell TraitAnimalsChildHemoglobinsHumansPlasmodium falciparumHemoglobinsAsymptomatic carriersGametocytesMalaria transmissionMosquito infectivitySickle cell trait

Identifiers

PMID37165325
PMCPMC10173526
OpenAlexW4376131061

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.