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Simulation-based validation of a method to detect changes in SARS-CoV-2 reinfection risk
Belinda Lombard1, Harry Moultrie2, Juliet R C Pulliam1
1South African DSI-NRF Centre of Excellence in Epidemiological Modelling and Analysis (SACEMA), Stellenbosch University, Stellenbosch, South Africa.
Plos Computational Biology
|February 3, 2025
Summary
This study validates a catalytic model for tracking SARS-CoV-2 reinfection risk. The model accurately detects changes in reinfection risk but requires sufficient data, especially in smaller epidemics.
Area of Science:
- Epidemiology
- Mathematical Modeling
- Infectious Disease Dynamics
Background:
- High global seroprevalence of SARS-CoV-2 necessitates understanding reinfection risks.
- Models tracking reinfection trends must be robust against data biases.
Purpose of the Study:
- To perform simulation-based validation of a catalytic model for detecting changes in SARS-CoV-2 reinfection risk.
- To assess model robustness against biases from imperfect data observation and mortality.
Main Methods:
- Simulated primary and reinfection datasets based on South African SARS-CoV-2 epidemic data.
- Incorporated biases like imperfect observation and mortality into simulations.
- Employed a Bayesian approach with a negative binomial distribution to fit the catalytic model.
Main Results:
- The catalytic model successfully detected changes in reinfection risk when simulated.
- Model parameters converged in most scenarios, aligning with anticipated outcomes.
- Low observation probabilities (10%) led to poor convergence and low observed cases.
Conclusions:
- The catalytic model is robust to imperfect observation and mortality in most scenarios.
- Model performance may differ in settings with smaller epidemics; further validation is recommended.
- Ensuring model parameter convergence is crucial to avoid false positives in detecting reinfection risk shifts.

