A comprehensive and high-quality collection of Escherichia coli genomes and their genes

Author:

Horesh Gal1ORCID,Blackwell Grace A.21ORCID,Tonkin-Hill Gerry1ORCID,Corander Jukka341ORCID,Heinz Eva5ORCID,Thomson Nicholas R.61ORCID

Affiliation:

1. Parasites and Microbes, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire CB10 1RQ, UK

2. EMBL-EBI, Wellcome Genome Campus, Hinxton, Cambridgeshire, UK

3. Department of Biostatistics, University of Oslo, Oslo, Norway

4. Department of Mathematics and Statistics, Helsinki Institute for Information Technology (HIIT), University of Helsinki, Helsinki, Finland

5. Department of Vector Biology and Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool L3 5QA, UK

6. Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London WC1E 7HT, UK

Abstract

Escherichia coli is a highly diverse organism that includes a range of commensal and pathogenic variants found across a range of niches and worldwide. In addition to causing severe intestinal and extraintestinal disease, E. coli is considered a priority pathogen due to high levels of observed drug resistance. The diversity in the E. coli population is driven by high genome plasticity and a very large gene pool. All these have made E. coli one of the most well-studied organisms, as well as a commonly used laboratory strain. Today, there are thousands of sequenced E. coli genomes stored in public databases. While data is widely available, accessing the information in order to perform analyses can still be a challenge. Collecting relevant available data requires accessing different sources, where data may be stored in a range of formats, and often requires further manipulation and processing to apply various analyses and extract useful information. In this study, we collated and intensely curated a collection of over 10 000 E. coli and Shigella genomes to provide a single, uniform, high-quality dataset. Shigella were included as they are considered specialized pathovars of E. coli . We provide these data in a number of easily accessible formats that can be used as the foundation for future studies addressing the biological differences between E. coli lineages and the distribution and flow of genes in the E. coli population at a high resolution. The analysis we present emphasizes our lack of understanding of the true diversity of the E. coli species, and the biased nature of our current understanding of the genetic diversity of such a key pathogen.

Funder

Wellcome Sanger Institute

Wellcome Sanger Institute PhD Studentship

Wellcome Trust PhD Scholarship Grant

European Research Council

Publisher

Microbiology Society

Subject

General Medicine

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