Phylodynamics on local sexual contact networks

PLoS Comput Biol. 2017 Mar 28;13(3):e1005448. doi: 10.1371/journal.pcbi.1005448. eCollection 2017 Mar.

Abstract

Phylodynamic models are widely used in infectious disease epidemiology to infer the dynamics and structure of pathogen populations. However, these models generally assume that individual hosts contact one another at random, ignoring the fact that many pathogens spread through highly structured contact networks. We present a new framework for phylodynamics on local contact networks based on pairwise epidemiological models that track the status of pairs of nodes in the network rather than just individuals. Shifting our focus from individuals to pairs leads naturally to coalescent models that describe how lineages move through networks and the rate at which lineages coalesce. These pairwise coalescent models not only consider how network structure directly shapes pathogen phylogenies, but also how the relationship between phylogenies and contact networks changes depending on epidemic dynamics and the fraction of infected hosts sampled. By considering pathogen phylogenies in a probabilistic framework, these coalescent models can also be used to estimate the statistical properties of contact networks directly from phylogenies using likelihood-based inference. We use this framework to explore how much information phylogenies retain about the underlying structure of contact networks and to infer the structure of a sexual contact network underlying a large HIV-1 sub-epidemic in Switzerland.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Evolution
  • Computer Simulation
  • Disease Outbreaks / statistics & numerical data*
  • Genetic Variation / genetics
  • HIV Infections / epidemiology*
  • HIV Infections / virology*
  • HIV-1 / genetics*
  • Humans
  • Models, Statistical*
  • Phylogeny
  • Prevalence
  • Sexual Partners*
  • Switzerland / epidemiology

Grants and funding

DAR is funded by the ETH Zürich Postdoctoral Fellowship Program and the Marie Curie Actions for People COFUND Program. RK is supported by Swiss National Science Foundation (SNF, grant BSSGI0_155851). TS is supported in part by the European Research Council under the Seventh Framework Programme of the European Commission (PhyPD: grant agreement number 335529). In addition, the Swiss HIV Cohort and the SHCS resistance database were supported by the SNF (grant 33CS30_148522, grant 320030_159868 to HFG, and grant PZ00P3-142411 to RK); the Swiss HIV Cohort Study (SHCS; projects 470, 528, 569, and 683); the SHCS Research Foundation; the Yvonne-Jacob Foundation; Gilead, Switzerland (one unrestricted grant to the SHCS Research Foundation and one unrestricted grant to HFG); and the University of Zürich’s Clinical Research Priority Program (Viral infectious diseases: Zürich Primary HIV Infection Study; to HFG). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.