Time Clustered Sampling Can Inflate the Inferred Substitution Rate in Foot-And-Mouth Disease Virus Analyses

PLoS One. 2015 Dec 2;10(12):e0143605. doi: 10.1371/journal.pone.0143605. eCollection 2015.

Abstract

With the emergence of analytical software for the inference of viral evolution, a number of studies have focused on estimating important parameters such as the substitution rate and the time to the most recent common ancestor (tMRCA) for rapidly evolving viruses. Coupled with an increasing abundance of sequence data sampled under widely different schemes, an effort to keep results consistent and comparable is needed. This study emphasizes commonly disregarded problems in the inference of evolutionary rates in viral sequence data when sampling is unevenly distributed on a temporal scale through a study of the foot-and-mouth (FMD) disease virus serotypes SAT 1 and SAT 2. Our study shows that clustered temporal sampling in phylogenetic analyses of FMD viruses will strongly bias the inferences of substitution rates and tMRCA because the inferred rates in such data sets reflect a rate closer to the mutation rate rather than the substitution rate. Estimating evolutionary parameters from viral sequences should be performed with due consideration of the differences in short-term and longer-term evolutionary processes occurring within sets of temporally sampled viruses, and studies should carefully consider how samples are combined.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Africa / epidemiology
  • Animals
  • Disease Outbreaks / veterinary
  • Evolution, Molecular*
  • Foot-and-Mouth Disease / epidemiology
  • Foot-and-Mouth Disease / virology
  • Foot-and-Mouth Disease Virus / classification
  • Foot-and-Mouth Disease Virus / genetics*
  • Foot-and-Mouth Disease Virus / isolation & purification
  • Models, Genetic
  • Phylogeny
  • RNA, Viral / genetics
  • Recombination, Genetic
  • Selection, Genetic
  • Sequence Alignment
  • Serotyping
  • Time Factors

Substances

  • RNA, Viral

Grant support

This work was supported by the Danish International Development Agency (DANIDA) under the Transboundary Animal Diseases in East Africa (TADEA) project, DFC no. 10-006KU. NJK and JW were partially funded by the Department for Environment, Food and Rural Affairs (Defra), UK (contract numbers SE2939 and SE2940). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.