Evidence map›Paper›PMID 41366737›Full record

ArticleBMC infectious diseases2025

Analytical and data-driven fractional-order malaria transmission model with vector and non-vector pathways.

Queeneth Ojoma Ahman, Patrick Agwu Okpara, Benedict Celestine Agbata, Emmanuel Olorunfemi Senewo, Ndidiamaka Edith Didigwu

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Article in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 citing paper in PubMed.

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5 · Who and what money

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5 authors.

Queeneth Ojoma AhmanDepartment of Mathematics, Enugu State University of Science and Technology, Enugu, Nigeria.
Patrick Agwu OkparaDepartment of Industrial Mathematics and Health Statistics, David Umahi Federal University of Health Sciences, Uburu, Nigeria.
Benedict Celestine AgbataDepartment of Mathematics/Statistics, Confluence University of Science and Technology, Osara, Nigeria.
Emmanuel Olorunfemi SenewoDepartment of Mathematics/Statistics, Confluence University of Science and Technology, Osara, Nigeria.
Ndidiamaka Edith DidigwuDepartment of Mathematics, Enugu State University of Science and Technology, Enugu, Nigeria. ndidiamakaedithdidigwu@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClassical malaria models often focus solely on vector-borne transmission and employ integer-order dynamics that neglect memory effects. Yet malaria spread can also occur through non-vector exposure routes, and its progression is influenced by historical infection and immunity patterns. To capture these effects, a fractional-order modeling approach is required.

methodsWe develop a Caputo fractional-order malaria model of order [Formula: see text] that integrates both vector and non-vector transmission pathways while embedding memory effects in human and mosquito dynamics. Analytical properties—including positivity, boundedness, disease-free equilibrium, and fractional local stability—are derived. The Adams–Bashforth–Moulton (ABM) predictor–corrector scheme is implemented for numerical simulation and validated against the classical case (q = 1) to ensure accuracy and convergence.

resultsNumerical experiments reveal that decreasing the fractional order q substantially modifies malaria dynamics: epidemic peaks are delayed, oscillatory persistence is prolonged, and long-term infection memory is amplified. Incorporating non-vector exposure pathways increases infection persistence and improves correspondence with field data. Parameter estimation and data fitting using weekly malaria incidence from the Nigeria Centre for Disease Control (NCDC) confirm the model’s reliability in reproducing outbreak patterns.

conclusionThe proposed fractional-order malaria model provides a unified analytical and computational framework that captures both memory-dependent and multi-route transmission effects. The ABM scheme proves efficient and accurate for fractional epidemic systems, and the accompanying MATLAB implementation supports reproducibility and application to malaria forecasting and control strategies.

Indexed as

Epidemiological ModelsMalariaMosquito VectorsAnimalsComputer SimulationHumansNigeriaAdams–bashforth–moulton methodCaputo derivativeData fittingFractional differential equationsMalaria transmission modelMemory effectsParameter estimationVector and non-vector pathways

Identifiers

PMID41366737
PMCPMC12801622

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