Evidence map›Paper›PMID 42842607›Full record

ArticlePloS one2026

Spatial and genetic dynamics of Plasmodium falciparum histidine-rich protein2 in sub-Saharan Africa.

Kaothar O Lambe, Favour Adeloye, Jennifer A Oboh, Halima Abdulsalam, Martin M Meremikwu, Grant L Hughes, Eva Heinz, Mary A Oboh

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Article in PloS one, 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

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Kaothar O LambeMedical Research Council Unit, The Gambia at The London School of Hygiene and Tropical Medicine, Banjul, Gambia.ORCID https://orcid.org/0000-0003-1625-5609
Favour AdeloyeMedical Research Council Unit, The Gambia at The London School of Hygiene and Tropical Medicine, Banjul, Gambia.
Jennifer A ObohCell Biology and Genetics Department, University of Lagos, Akoka, Nigeria.
Halima AbdulsalamMedical Research Council Unit, The Gambia at The London School of Hygiene and Tropical Medicine, Banjul, Gambia.
Martin M MeremikwuUniversity of Calabar Teaching Hospital, Calabar, Nigeria.
Grant L HughesLiverpool School of Tropical Medicine, Liverpool, United Kingdom.
Eva HeinzUniversity of Strathclyde, Glasgow, United Kingdom.
Mary A ObohMedical Research Council Unit, The Gambia at The London School of Hygiene and Tropical Medicine, Banjul, Gambia.ORCID https://orcid.org/0000-0001-5720-8425

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMalaria rapid diagnosis tests (mRDTs) detecting Plasmodium falciparum histidine-rich protein 2 (Pfhrp2) are the most widely adopted diagnostic tool in malaria-endemic areas. However, extensive polymorphisms in Pfhrp2 could modify Pfhrp2 epitopes, rendering it undetectable by Pfhrp2-based mRDTs. This study investigates the spatial distribution and population dynamics of Pfhrp2 in sub-Saharan Africa (sSA).

methodPfhrp2 sequences (215) were retrieved from public repositories and analysed with MAFFT v7, DnaSP, and various packages in R. We computed genetic diversity metrics, neutrality tests, differentiation, haplotype networks, and phylogenetic analyses.

resultsVarying degrees of insertion-deletion with about 10 polymorphic repeat motif types that varied in frequencies were observed. Repeat types 2, 4 and 7 were the most prevalent types. Baker model prediction with mRDTs monoclonal antibodies indicated the prevalence of highly detected Pfhrp2 isolates in sSA. Significant diversity was recorded across the sSA region (Hd = 1; θw = 0.09585). The single most dominant haplotype was conserved across countries, and very low differentiation (FST: 0.00-0.04) suggested gene flow between countries.

conclusionOur findings imply that the dominant evolutionary pressure in sSA is promoting the parasite's biological fitness and the diversity of Pfhrp2.However, the impact of this genetic diversity on diagnostic performance was not assessed as we could not obtain relevant mRDT test data for each country.

Indexed as

Antigens, ProtozoanMalaria, FalciparumPlasmodium falciparumProtozoan ProteinsAfrica South of the SaharaGenetic VariationHaplotypesHumansPhylogenyPolymorphism, GeneticRapid Diagnostic TestsAntigens, ProtozoanHRP-2 antigen, Plasmodium falciparumProtozoan Proteins

Identifiers

PMID42842607
PMCPMC13645071

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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.