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Published on: December 9, 2015
Resolving the impact of waiting time distributions on the persistence of measles
Andrew J K Conlan1, Pejman Rohani, Alun L Lloyd
1Department of Veterinary Medicine, University of Cambridge, Cambridge Infectious Diseases Consortium, Cambridge, UK. a.j.k.conlan@damtp.cam.ac.uk
Abstract:
Measles epidemics in human populations exhibit what is perhaps the best empirically characterized, and certainly the most studied, stochastic persistence threshold in population biology. A critical community size (CCS) of around 250,000-500,000 separates populations where measles is predominantly persistent from smaller communities where there are frequent extinctions of measles between major epidemics. The fundamental mechanisms contributing to this pattern of persistence, which are long-lasting immunity to re-infection, recruitment of susceptibles, seasonality in transmission, age dependence of transmission and the spatial coupling between communities, have all been quantified and, to a greater or lesser level of success, captured by theoretical models. Despite these successes there has not been a consensus over whether simple models can successfully predict the value of the CCS, or indeed which mechanisms determine the persistence of measles over a broader range of population sizes. Specifically, the level of the CCS has been thought to be particularly sensitive to the detailed stochastic dynamics generated by the waiting time distribution (WTD) in the infectious and latent periods. We show that the relative patterns of persistence between models with different WTDs are highly sensitive to the criterion of comparison-in particular, the statistical measure of persistence that is employed. To this end, we introduce two new statistical measures of persistence-fade-outs post epidemic and fade-outs post invasion. Contrary to previous reports, we demonstrate that, no matter the choice of persistence measure, appropriately parametrized models of measles demonstrate similar predictions for the level of the CCS.
Insights
Measles persistence in populations depends on community size, not just infection dynamics. New measures show models consistently predict the critical community size (CCS) for measles persistence.
Area of Science:
- Epidemiology
- Population Biology
- Mathematical Modeling
Background:
- Measles exhibits a well-defined stochastic persistence threshold, with a critical community size (CCS) around 250,000-500,000.
- Factors like immunity, susceptible recruitment, seasonality, age, and spatial coupling influence measles persistence.
- Previous models struggled to agree on CCS prediction and the mechanisms driving measles persistence.
Purpose of the Study:
- To investigate whether simple models can accurately predict the critical community size (CCS) for measles persistence.
- To determine which mechanisms are most crucial for measles persistence across various population sizes.
- To assess the impact of different waiting time distributions (WTDs) on measles persistence models.
Main Methods:
- Introduced two novel statistical measures for assessing persistence: fade-outs post-epidemic and fade-outs post-invasion.
- Compared persistence patterns between models with varying WTDs using different statistical criteria.
- Utilized appropriately parameterized measles models to analyze CCS predictions.
Main Results:
- The relative patterns of measles persistence across models are highly sensitive to the chosen statistical measure of persistence.
- Contrary to prior research, this study demonstrates that model predictions for CCS are consistent regardless of the persistence measure used.
- Appropriately parameterized models yield similar CCS predictions irrespective of WTD variations.
Conclusions:
- The critical community size for measles persistence is robust across different statistical measures and waiting time distributions.
- Simple, well-parameterized models can effectively predict the CCS for measles.
- Understanding the interplay of epidemiological factors and stochastic dynamics is key to predicting infectious disease persistence.
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