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Using dimension reduction to improve outbreak predictability of multistrain diseases.
Leah B Shaw1, Lora Billings, Ira B Schwartz
1Naval Research Laboratory, Plasma PhysicsDivision, Nonlinear Systems Dynamics Section, Washington, DC 20375, USA. lshaw@nls6.nrl.navy.mil
Journal of Mathematical Biology
|February 24, 2007
Summary
This study models multistrain diseases with antibody-dependent enhancement (ADE). Our dynamic model simplifies complex interactions, explaining disease synchrony and predicting asymptomatic cases during epidemics.
Area of Science:
- Epidemiology
- Mathematical Biology
- Infectious Disease Dynamics
Background:
- Multistrain diseases involve coexisting serotypes, complicating epidemiological modeling.
- Antibody-dependent enhancement (ADE) can increase viral load and infectivity upon secondary infection with a different serotype, as seen in dengue fever.
Purpose of the Study:
- To develop and analyze a dynamic compartmental model for multistrain diseases exhibiting ADE.
- To simplify the complex dynamics of ADE using mathematical techniques.
- To explain observed synchrony in disease progression and predict asymptomatic infections.
Main Methods:
- Development of a dynamic compartmental model for multiple serotypes with ADE.
- Application of center manifold techniques to reduce model dimensionality.
- Numerical analysis of both deterministic and stochastic model versions.
- Investigation of model applicability to noisy systems and cross-immunity.
Main Results:
- The complex multistrain dynamics rapidly collapse to a lower-dimensional system.
- The reduced model successfully explains previously observed synchrony between primary and secondary infectives.
- Center manifold equations remain valid in noisy systems.
- Both model versions predict asymptomatic individuals, crucial for epidemic tracking.
Conclusions:
- Center manifold techniques provide a powerful tool for analyzing and simplifying multistrain disease dynamics with ADE.
- The model offers valuable insights into disease synchrony and the prediction of asymptomatic cases.
- This approach is potentially applicable to other multistrain diseases, including those with cross-immunity.
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