| Literature DB >> 25887947 |
Roman Biek1, Oliver G Pybus2, James O Lloyd-Smith3, Xavier Didelot4.
Abstract
Current sequencing technologies have created unprecedented opportunities for studying microbial populations. For pathogens with comparatively low per-site mutation rates, such as DNA viruses and bacteria, whole-genome sequencing can reveal the accumulation of novel genetic variation between population samples taken at different times. The concept of 'measurably evolving populations' and related analytical approaches have provided powerful insights for fast-evolving RNA viruses, but their application to other pathogens is still in its infancy. We argue that previous distinctions between slow- and fast-evolving pathogens become blurred once evolution is assessed at a genome-wide scale, and we highlight important analytical challenges to be overcome to infer pathogen population dynamics from genomic data.Entities:
Keywords: DNA virus; bacteria; epidemiological models; evolutionary rate; infectious disease; phylodynamics
Mesh:
Year: 2015 PMID: 25887947 PMCID: PMC4457702 DOI: 10.1016/j.tree.2015.03.009
Source DB: PubMed Journal: Trends Ecol Evol ISSN: 0169-5347 Impact factor: 17.712