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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
Abstract:
Multistrain diseases have multiple distinct coexisting serotypes (strains). For some diseases, such as dengue fever, the serotypes interact by antibody-dependent enhancement (ADE), in which infection with a single serotype is asymptomatic, but contact with a second serotype leads to higher viral load and greater infectivity. We present and analyze a dynamic compartmental model for multiple serotypes exhibiting ADE. Using center manifold techniques, we show how the dynamics rapidly collapses to a lower dimensional system. Using the constructed reduced model, we can explain previously observed synchrony between certain classes of primary and secondary infectives (Schwartz et al. in Phys Rev E 72:066201, 2005). Additionally, we show numerically that the center manifold equations apply even to noisy systems. Both deterministic and stochastic versions of the model enable prediction of asymptomatic individuals that are difficult to track during an epidemic. We also show how this technique may be applicable to other multistrain disease models, such as those with cross-immunity.
Insights
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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