Modeling and Analysis of SIRR Model (Ebola Transmission Dynamics Model) with Delay Differential Equation.

Q2 Pharmacology, Toxicology and Pharmaceutics
F1000Research Pub Date : 2025-09-02 eCollection Date: 2025-01-01 DOI:10.12688/f1000research.168361.1
Akinleye Emmanuel Lasekan, Joshua Oluwasegun Agbomola, Kabir Oluwatobi Idowu, Babatunde Ademola Kannike, Esther Oluwatoyin Mulero, Temitope Senami Gandonu, Solari Myrjuari Elee
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引用次数: 0

Abstract

Background: Ebola virus disease (EVD) is a severe and often fatal illness with high transmission potential and recurring outbreaks. Traditional compartmental models often neglect biologically important delays, such as the latent period before an infected individual becomes infectious, limiting their ability to capture real-world epidemic patterns. Including such delays can provide a more accurate understanding of outbreak persistence and control strategies.

Methods: In this study, we develop and analyze a novel deterministic SIRR model that captures the complex transmission dynamics of Ebola by explicitly combining nonlinear incidence rates with a delay differential equation framework. Unlike traditional models, this approach integrates a biologically motivated delay to represent the latent period before infectiousness, providing a more realistic depiction of disease spread. The basic reproduction number (R 0) is derived using the next-generation matrix, and local stability for disease-free and endemic equilibria is established. Using center manifold theory, we investigate transcritical bifurcation at R 0 = 1, while Hopf bifurcation analysis determines when delays trigger oscillatory epidemics. Sensitivity analysis identifies parameters most influencing R 0, and numerical simulations are performed using the fourth-order Runge-Kutta method.

Results: The main novelty of this work lies in its detailed investigation of how delays influence outbreak persistence and can trigger oscillatory epidemics, patterns often observed in practice but rarely captured by classic models. For R 0< 1, the disease-free equilibrium is locally asymptotically stable; for R 0> 1, an endemic equilibrium emerges. Increasing delays destabilizes the system, amplifying peak infections, prolonging outbreaks, and producing sustained oscillations. Isolation of recovered individuals (c) significantly reduces R_0, while transmission rate (β), recruitment rate (Λ), and isolation transition rate (ρ) are identified as the most sensitive parameters.

Conclusions: Accounting for delayed recovery dynamics is crucial for accurately predicting outbreak patterns and designing effective interventions. This delay-based, nonlinear-incidence model offers a robust analytical and computational framework for guiding public health strategies, with direct implications for reducing transmission, shortening outbreak duration, and preventing epidemic resurgence.

埃博拉病毒传播动力学模型的时滞微分方程建模与分析
背景:埃博拉病毒病(EVD)是一种严重且往往致命的疾病,具有高传播潜力和反复暴发。传统的区室模型往往忽略了生物学上重要的延迟,例如受感染个体变得具有传染性之前的潜伏期,从而限制了它们捕捉现实世界流行病模式的能力。包括这种延迟可以更准确地了解爆发的持久性和控制策略。方法:在本研究中,我们开发并分析了一种新的确定性SIRR模型,该模型通过明确地将非线性发病率与延迟微分方程框架结合起来,捕捉了埃博拉病毒的复杂传播动力学。与传统模型不同,这种方法整合了生物学动机延迟来表示感染前的潜伏期,提供了更真实的疾病传播描述。利用新一代矩阵导出了基本繁殖数r0,并建立了无病平衡点和地方性平衡点的局部稳定性。利用中心流形理论,我们研究了r0 = 1处的跨临界分岔,而Hopf分岔分析确定了延迟何时触发振荡流行病。灵敏度分析找出了影响r0最大的参数,并采用四阶龙格-库塔方法进行了数值模拟。结果:这项工作的主要新颖之处在于它详细调查了延迟如何影响爆发的持久性,并可能引发振荡流行病,这种模式在实践中经常观察到,但很少被经典模型捕获。当r0 < 1时,无病平衡点是局部渐近稳定的;对于r0和r0,出现地方性平衡。不断增加的延迟会破坏系统的稳定,放大感染高峰,延长疫情爆发时间,并产生持续的振荡。分离恢复个体(c)可显著降低R_0,而传播率(β)、招募率(Λ)和分离转移率(ρ)被认为是最敏感的参数。结论:考虑延迟恢复动力学对于准确预测爆发模式和设计有效的干预措施至关重要。这种基于延迟的非线性发病率模型为指导公共卫生战略提供了强大的分析和计算框架,对减少传播、缩短爆发持续时间和防止流行病再次发生具有直接意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
F1000Research
F1000Research Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
5.00
自引率
0.00%
发文量
1646
审稿时长
1 weeks
期刊介绍: F1000Research publishes articles and other research outputs reporting basic scientific, scholarly, translational and clinical research across the physical and life sciences, engineering, medicine, social sciences and humanities. F1000Research is a scholarly publication platform set up for the scientific, scholarly and medical research community; each article has at least one author who is a qualified researcher, scholar or clinician actively working in their speciality and who has made a key contribution to the article. Articles must be original (not duplications). All research is suitable irrespective of the perceived level of interest or novelty; we welcome confirmatory and negative results, as well as null studies. F1000Research publishes different type of research, including clinical trials, systematic reviews, software tools, method articles, and many others. Reviews and Opinion articles providing a balanced and comprehensive overview of the latest discoveries in a particular field, or presenting a personal perspective on recent developments, are also welcome. See the full list of article types we accept for more information.
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