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Understanding bacterial population genetics is vital for interpreting the response of bacterial populations to selection pressures such as antibiotic treatment or vaccines targeted at only a subset of strains. The evolution of transmissible bacteria occurs by mutation and localized recombination and is influenced by epidemiological as well as molecular processes. We demonstrate that the observed population genetic structure of three important human pathogens, Streptococcus pneumoniae, Neisseria meningitidis, and Staphylococcus aureus, can be explained by using a simple evolutionary model that is based on neutral mutational drift, modulated by recombination, and which incorporates the impact of epidemic transmission in local populations. The predictions of this neutral "microepidemic" model are found to closely fit observed genetic relatedness distributions of bacteria sampled from their natural population, and it provides estimates of the relative rate of recombination that agree well with empirical estimates. The analysis suggests the emergence of neutral bacterial population structure from overlapping microepidemics within clustered host populations and provides insight into the nature and size distribution of these clusters. These findings challenge the assumption that strains of bacterial pathogens differ markedly in relative fitness.

Original publication

DOI

10.1073/pnas.0406993102

Type

Journal article

Journal

Proceedings of the National Academy of Sciences of the United States of America

Publication Date

02/2005

Volume

102

Pages

1968 - 1973

Addresses

Department of Infectious Disease Epidemiology, St. Mary's Hospital Campus, Imperial College London, Norfolk Place, London W2 1PG, United Kingdom. c.fraser@imperial.ac.uk

Keywords

Humans, Neisseria meningitidis, Staphylococcus aureus, Streptococcus pneumoniae, Bacterial Infections, Genetics, Population, Recombination, Genetic, Alleles, Models, Biological, Selection, Genetic, Biological Evolution