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Novel bioinformatic methods and machine learning approaches reveal candidate biomarkers of the intensity and timing of past exposure to Plasmodium falciparum

Dados Bibliográficos

ID19590999
AutoresSophie Bérubé (0000-0001-9214-8624, Johns Hopkins University, autor correspondente), Tamaki Kobayashi (0000-0002-6908-4519, Johns Hopkins University, autor correspondente), Douglas E Norris (0000-0002-4631-2777, Johns Hopkins University, autor correspondente), Ingo Ruczinski (0000-0003-3278-6274, Johns Hopkins University, autor correspondente), William J Moss (0000-0001-6579-3513, Johns Hopkins University, autor correspondente), Amy Wesolowski (0000-0001-6320-3575, Johns Hopkins University, autor correspondente), Thomas A Louis (0000-0002-3592-6386, Johns Hopkins University, autor correspondente)
EditoresJanelisa Musaya (0000-0003-2928-0133)
Ano2023
Volume3
Fascículo8
Páginase0001840
Data de publicação2023-08-02
Peer ReviewedSim
Open AccessSim
TipoARTICLE
PeriódicoPLOS Global Public Health (JOURNAL)
Identificadores do periódicoISSN: 2767-3375 • E-ISSN: 2767-3375
EditoraPublic Library of Science (PLoS) (PUBLISHER)
DOI10.1371/journal.pgph.0001840
PMID37531325
OpenAlexW4385489445
IdiomaEN
Referências citadas30

Accurately quantifying the burden of malaria over time is an important goal of malaria surveillance efforts and can enable effective targeting and evaluation of interventions. Malaria surveillance methods capture active or recent infections which poses several challenges to achieving malaria surveillance goals. In high transmission settings, asymptomatic infections are common and therefore accurate measurement of malaria burden demands active surveillance; in low transmission regions where infections are rare accurate surveillance requires sampling large subsets of the population; and in any context monitoring malaria burden over time necessitates serial sampling. Antibody responses to Plasmodium falciparum parasites persist after infection and therefore measuring antibodies has the potential to overcome several of the current obstacles to accurate malaria surveillance. Identifying which antibody responses are markers of the timing and intensity of past exposure to P. falciparum remains challenging, particularly among adults who tend to be re-exposed multiple times over the course of their lifetime and therefore have similarly high antibody responses to many Plasmodium antigens. A previous analysis of 479 serum samples from individuals in three regions in southern Africa with different historical levels of P. falciparum malaria transmission (high, intermediate, and low) revealed regional differences in antibody responses to P. falciparum antigens among children under 5 years of age. Using a novel bioinformatic pipeline optimized for protein microarrays that minimizes between-sample technical variation, we used antibody responses to Plasmodium antigens as predictors in random forest models to classify samples from adults into these three regions of differing historical malaria transmission with high accuracy (AUC = 0.99). Many of the most important antigens for classification in these models do not overlap with previously published results and are therefore novel candidate markers for the timing and intensity of past exposure to P. falciparum . Measuring antibody responses to these antigens could lead to improved malaria surveillance

Biology · Environmental health · Malaria · Plasmodium falciparum · Population · Computational Drug Discovery Methods · Computer Science · Malaria Research and Control · Medicine · Immunology · Virology

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Velocidade de citaçãohistorical
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