Evidence map›Paper›PMID 37653544›Full record

ArticleParasites & vectors2023

Recent increase in low complexity polygenomic infections and sialic acid-independent invasion pathways in Plasmodium falciparum from Western Gambia.

Nora Nghochuzie Nganyewo, Fatoumata Bojang, Eniyou Cheryll Oriero, Ndey Fatou Drammeh, Olumide Ajibola, Haddijatou Mbye, Aminata Seedy Jawara, Simon Corea, Gordon Akanzuwine Awandare, Umberto D'Alessandro and 2 more

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 38% of its field
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

12 authors at 2 institutions in 2 countries.

Nora Nghochuzie NganyewoMedical Research Council Unit The Gambia at London, School of Hygiene and Tropical Medicine, Banjul, The Gambia.
Fatoumata BojangMedical Research Council Unit The Gambia at London, School of Hygiene and Tropical Medicine, Banjul, The Gambia.
Eniyou Cheryll OrieroMedical Research Council Unit The Gambia at London, School of Hygiene and Tropical Medicine, Banjul, The Gambia.
Ndey Fatou DrammehMedical Research Council Unit The Gambia at London, School of Hygiene and Tropical Medicine, Banjul, The Gambia.
Olumide AjibolaMedical Research Council Unit The Gambia at London, School of Hygiene and Tropical Medicine, Banjul, The Gambia.
Haddijatou MbyeMedical Research Council Unit The Gambia at London, School of Hygiene and Tropical Medicine, Banjul, The Gambia.
Aminata Seedy JawaraMedical Research Council Unit The Gambia at London, School of Hygiene and Tropical Medicine, Banjul, The Gambia.
Simon CoreaMedical Research Council Unit The Gambia at London, School of Hygiene and Tropical Medicine, Banjul, The Gambia.
Gordon Akanzuwine AwandareWest African Centre for Cell Biology of Infectious Pathogens (WACCBIP), University of Ghana, Accra, Ghana.
Umberto D'AlessandroMedical Research Council Unit The Gambia at London, School of Hygiene and Tropical Medicine, Banjul, The Gambia.
Lucas N Amenga-EtegoWest African Centre for Cell Biology of Infectious Pathogens (WACCBIP), University of Ghana, Accra, Ghana.
Alfred Amambua-NgwaMedical Research Council Unit The Gambia at London, School of Hygiene and Tropical Medicine, Banjul, The Gambia. alfred.ngwa@lshtm.ac.uk.
MRC Unit the Gambia · GMUniversity of Ghana · GH

Funding

Pan-African Malaria Genetic Epidemiology Network (PAMGEN) H3A/18/002
6 · The paper itself

Abstract

backgroundThe malaria parasite Plasmodium falciparum utilizes multiple alternative receptor-ligand interactions for the invasion of human erythrocytes. While some P. falciparum clones make use of sialic acid (SA) residues on the surface of the human glycophorin receptors to invade the erythrocyte, others use alternative receptors independent of sialic acid residues. We hypothesized that over the years, intensified malaria control interventions and declining prevalence in The Gambia have resulted in a selection of parasites with a dominant invasion pathways and ligand expression profiles.

methodsBlood samples were collected from 65 malaria-infected participants with uncomplicated malaria across 3 years (2015, 2016, and 2021). Genetic diversity was determined by genotyping the merozoite surface protein 2 (msp2) polymorphic gene of P. falciparum. Erythrocyte invasion phenotypes were determined using neuraminidase, trypsin, and chymotrypsin enzymes, known to cleave different receptors from the surface of the erythrocyte. Schizont-stage transcript levels were obtained for a panel of 6 P. falciparum invasion ligand genes (eba175, eba181, Rh2b, Rh4, Rh5, and clag2) using 48 successfully cultured isolates.

resultsThough the allelic heterozygosity of msp2 repeat region decreased as expected with reduced transmission, there was an increase in infections with more than a single msp2 allelotype from 2015 to 2021. The invasion phenotypes of these isolates were mostly SA independent with a continuous increase from 2015 to 2021. Isolates from 2021 were highly inhibited by chymotrypsin treatment compared to isolates from 2015 and 2016. Higher invasion inhibition for 2021 isolates was further obtained following erythrocyte treatment with a combination of chymotrypsin and trypsin. The transcript levels of invasion ligand genes varied across years. However, levels of clag2, a rhoptry-associated protein, were higher in 2015 and 2016 isolates than in 2021 isolates, while Rh5 levels were higher in 2021 compared to other years.

conclusionsOverall, these findings suggest increasing mixed infections with an increase in the use of sialic-acid independent invasion pathways by P. falciparum clinical isolates in the Western part of Gambia.

Indexed as

Malaria, FalciparumPlasmodium falciparumChymotrypsinGambiaHumansLigandsN-Acetylneuraminic AcidTrypsinChymotrypsinLigandsN-Acetylneuraminic AcidTrypsinErythrocyteExpressionInhibitionInvasionLigand genesMalariaP. falciparum

Identifiers

PMID37653544
PMCPMC10472613
OpenAlexW4386324975

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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.