Abstract

Phylodynamics - the field aiming to quantitatively integrate the ecological and evolutionary dynamics of rapidly evolving populations like those of RNA viruses – increasingly relies upon coalescent approaches to infer past population dynamics from reconstructed genealogies. As sequence data have become more abundant, these approaches are beginning to be used on populations undergoing rapid and rather complex dynamics. In such cases, the simple demographic models that current phylodynamic methods employ can be limiting. First, these models are not ideal for yielding biological insight into the processes that drive the dynamics of the populations of interest. Second, these models differ in form from mechanistic and often stochastic population dynamic models that are currently widely used when fitting models to time series data. As such, their use does not allow for both genealogical data and time series data to be considered in tandem when conducting inference. Here, we present a flexible statistical framework for phylodynamic inference that goes beyond these current limitations. The framework we present employs a recently developed method known as particle MCMC to fit stochastic, nonlinear mechanistic models for complex population dynamics to gene genealogies and time series data in a Bayesian framework. We demonstrate our approach using a nonlinear Susceptible-Infected-Recovered (SIR) model for the transmission dynamics of an infectious disease and show through simulations that it provides accurate estimates of past disease dynamics and key epidemiological parameters from genealogies with or without accompanying time series data.

Highlights

  • Epidemiologists increasingly rely on the ability to fit mechanistic models of disease transmission to data in order to estimate key parameters and elucidate the underlying processes driving disease dynamics

  • There has been great interest in developing statistical methods for inferring past population dynamics from gene genealogies reconstructed from molecular sequences

  • We show how current phylodynamic methods can be extended to allow a much wider class of models to be fit to genealogies and illustrate our approach using an epidemiological model for the transmission of an infectious disease

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Summary

Introduction

Epidemiologists increasingly rely on the ability to fit mechanistic models of disease transmission to data in order to estimate key parameters and elucidate the underlying processes driving disease dynamics. The nature of epidemiological data makes model fitting statistically challenging. Case report data such as time series of disease incidence are often incomplete or subject to severe biases like underreporting. Gene genealogies can be reconstructed from sequence data and the times of coalescence events (i.e. branching events) can be used as a proxy for the timing of a subset of transmission events in the population. Using coalescent-based ‘‘phylodynamic’’ methods, it is possible to infer the past dynamics of a disease from the lineages present in the genealogy, opening up the possibility of fitting models directly to genealogies

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