Scinovex
article Open AccessTop 1% cited

eBURST: Inferring Patterns of Evolutionary Descent among Clusters of Related Bacterial Genotypes from Multilocus Sequence Typing Data

Journal of Bacteriology · 2004 · Vol. 186(5) · pp. 1518–1530
Edward J. FeilBao C. LiDavid M. AanensenWilliam P. HanageBrian G. Spratt

Abstract

The introduction of multilocus sequence typing (MLST) for the precise characterization of isolates of bacterial pathogens has had a marked impact on both routine epidemiological surveillance and microbial population biology. In both fields, a key prerequisite for exploiting this resource is the ability to discern the relatedness and patterns of evolutionary descent among isolates with similar genotypes. Traditional clustering techniques, such as dendrograms, provide a very poor representation of recent evolutionary events, as they attempt to reconstruct relationships in the absence of a realistic model of the way in which bacterial clones emerge and diversify to form clonal complexes. An increasingly popular approach, called BURST, has been used as an alternative, but present implementations are unable to cope with very large data sets and offer crude graphical outputs. Here we present a new implementation of this algorithm, eBURST, which divides an MLST data set of any size into groups of related isolates and clonal complexes, predicts the founding (ancestral) genotype of each clonal complex, and computes the bootstrap support for the assignment. The most parsimonious patterns of descent of all isolates in each clonal complex from the predicted founder(s) are then displayed. The advantages of eBURST for exploring patterns of evolutionary descent are demonstrated with a number of examples, including the simple Spain(23F)-1 clonal complex of Streptococcus pneumoniae, "population snapshots" of the entire S. pneumoniae and Staphylococcus aureus MLST databases, and the more complicated clonal complexes observed for Campylobacter jejuni and Neisseria meningitidis.

Genomics and Phylogenetic StudiesAntimicrobial Resistance in StaphylococcusPneumonia and Respiratory InfectionsMultilocus sequence typingBiologyGeneticsPopulationTypingGenotypeMicroevolutionEvolutionary biologyComputational biologyGene

MeSH terms

AlgorithmsBacteriaBacterial InfectionsGenotypeHumansNeisseria meningitidisSoftwareStaphylococcus aureusStreptococcus pneumoniaeBacterial Typing TechniquesMethicillin ResistanceCampylobacter jejuniEvolution, MolecularDrug Resistance, Multiple, Bacterial

Funding

  • Wellcome Trust
  • Imperial College London
  • University of Oxford
  • Medical Research Council
Citations
1,859
FWCI
25.70
field-weighted impact
References
37
Percentile
100%
vs. same field & year
Citations per year
Cited by
Multilocus Sequence Typing of <i>Klebsiella pneumoniae</i> Nosocomial Isolates
Journal of Clinical Microbiology · 2005 · 1,346 citations
The microbiome of uncontacted Amerindians
Science Advances · 2015 · 842 citations
Sex and virulence in <i>Escherichia coli</i>: an evolutionary perspective
Molecular Microbiology · 2006 · 2,003 citations
Waves of resistance: Staphylococcus aureus in the antibiotic era
Nature Reviews Microbiology · 2009 · 2,642 citations
The role of nasal carriage in Staphylococcus aureus infections
The Lancet Infectious Diseases · 2005 · 2,663 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.