Lasekan Akinleye Emmanuel, Oluwasegun Agbomola Joshua, Idowu Kabir Oluwatobi, Kannike Babatunde Ademola, Mulero Esther Oluwatoyin, Senami Gandonu Temitope, Elee Solari Myrjuari
Department of Mathematics, Lagos State University, Ojo, Lagos, Nigeria.
Department of Mathematics, Tulane University, New Orleans, Louisiana, USA.
F1000Res. 2025 Sep 2;14:857. doi: 10.12688/f1000research.168361.1. eCollection 2025.
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.
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 ) 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 = 1, while Hopf bifurcation analysis determines when delays trigger oscillatory epidemics. Sensitivity analysis identifies parameters most influencing R , and numerical simulations are performed using the fourth-order Runge-Kutta method.
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 < 1, the disease-free equilibrium is locally asymptotically stable; for R > 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.
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.
埃博拉病毒病(EVD)是一种严重且往往致命的疾病,具有高传播潜力且疫情反复爆发。传统的 compartmental 模型常常忽略生物学上重要的延迟,例如感染个体具有传染性之前的潜伏期,这限制了它们捕捉现实世界疫情模式的能力。纳入此类延迟能够更准确地理解疫情的持续情况和控制策略。
在本研究中,我们开发并分析了一种新型确定性 SIRR 模型,该模型通过将非线性发病率与延迟微分方程框架明确结合,捕捉埃博拉复杂的传播动态。与传统模型不同,此方法纳入了一个基于生物学的延迟来表示传染性出现之前的潜伏期,从而对疾病传播进行更现实的描述。使用下一代矩阵推导基本再生数(R ),并建立无病和地方病平衡点的局部稳定性。利用中心流形理论,我们研究 R = 1 时的跨临界分岔,同时通过霍普夫分岔分析确定延迟何时引发振荡疫情。敏感性分析确定了对 R 影响最大的参数,并使用四阶龙格 - 库塔方法进行数值模拟。
这项工作的主要新颖之处在于详细研究了延迟如何影响疫情持续情况并能引发振荡疫情,这些模式在实际中经常观察到,但经典模型很少能捕捉到。对于 R < 1,无病平衡点是局部渐近稳定的;对于 R > 1,出现地方病平衡点。延迟增加会使系统不稳定,放大感染峰值,延长疫情爆发时间并产生持续振荡。康复个体的隔离率(c)显著降低 R_0,而传播率(β)、招募率(Λ)和隔离转变率(ρ)被确定为最敏感的参数。
考虑延迟恢复动态对于准确预测疫情模式和设计有效干预措施至关重要。这种基于延迟的非线性发病率模型为指导公共卫生策略提供了一个强大的分析和计算框架,对减少传播、缩短疫情持续时间和防止疫情再次爆发具有直接意义。