Abstract
BACKGROUND: Mathematical models are essential for understanding viral dynamics, with the basic viral model widely used to describe infection kinetics. Quasi-steady-state approximation (QSSA) is often applied to improve computational efficiency and simplify the system. However, the existing viral QSSA model incorrectly assumes that infected cells evolve on the same fast timescale as the virus, leading to biologically invalid simplifications. RESULTS: In this study, we resolved this issue by developing a revised QSSA viral model that correctly accounts for timescale separation and prevents the erroneous loss of infected cell initial values during model reduction. We introduce a mathematical method to estimate the initial condition of infected cells and define a validity condition ( Cv = δ/c ), under which QSSA is accurate only when Cv ≪ 1 , ensuring proper timescale separation. Comparative analysis shows that the revised QSSA model retains biological fidelity while improving predictive accuracy and computational efficiency. Sensitivity analysis confirmed that it preserves key dynamic responses to parameter changes, further validating its robustness. Parameter estimation demonstrated that the revised QSSA model more accurately recovers true parameter values under strong timescale separation. CONCLUSIONS: This work resolves a key flaw in existing QSSA models, enabling more accurate and consistent modeling of viral dynamics. By correcting the infected cell loss issue, our findings provide a robust framework for virological applications, particularly useful when experimental data are limited.