Abstract

Emerging and endemic animal viral diseases continue to impose substantial impacts on animal and human health. Most current and past molecular surveillance studies of animal diseases investigated spatio-temporal and evolutionary dynamics of the viruses in a disjointed analytical framework, ignoring many uncertainties and made joint conclusions from both analytical approaches. Phylodynamic methods offer a uniquely integrated platform capable of inferring complex epidemiological and evolutionary processes from the phylogeny of viruses in populations using a single Bayesian statistical framework. In this study, we reviewed and outlined basic concepts and aspects of phylodynamic methods and attempted to summarize essential components of the methodology in one analytical pipeline to facilitate the proper use of the methods by animal health researchers. Also, we challenged the robustness of the posterior evolutionary parameters, inferred by the commonly used phylodynamic models, using hemagglutinin (HA) and polymerase basic 2 (PB2) segments of the currently circulating human-like H3 swine influenza (SI) viruses isolated in the United States and multiple priors. Subsequently, we compared similarities and differences between the posterior parameters inferred from sequence data using multiple phylodynamic models. Our suggested phylodynamic approach attempts to reduce the impact of its inherent limitations to offer less biased and biologically plausible inferences about the pathogen evolutionary characteristics to properly guide intervention activities. We also pinpointed requirements and challenges for integrating phylodynamic methods in routine animal disease surveillance activities.

Highlights

  • In the past few decades, genetic analysis of rapidly evolving pathogens has become an integral part of animal disease surveillance systems worldwide [1,2,3,4]

  • We evaluated the fit of the 16 phylodynamic models to the HA and PB2 sequences using the BF comparisons of their MLL estimated by the PS and SS simulator in order to select the most realistic model and correctly interpret its posterior inferences

  • We challenged the robustness of the posterior evolutionary parameters, inferred by the commonly used phylodynamic models, using two gene segments, of the currently circulating human-like H3 SI viruses isolated in the United States, and multiple priors

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Summary

Introduction

In the past few decades, genetic analysis of rapidly evolving pathogens has become an integral part of animal disease surveillance systems worldwide [1,2,3,4]. Most current and past molecular surveillance studies of animal disease pathogens of both public health and economical importance such as influenza [5,6,7], foot-and-mouth disease (FMD) [8,9,10], and porcine reproductive

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