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Phylogenetic background and habitat drive the genetic diversification of Escherichia coli

dc.contributor.authorTouchon, Marie
dc.contributor.authorPerrin, Amandine
dc.contributor.authorde Sousa, Jorge Andre Moura
dc.contributor.authorVangchhia, Belinda
dc.contributor.authorBurn, Samantha
dc.contributor.authorO'Brien, Claire L.
dc.contributor.authorDenamur, Erick
dc.contributor.authorGordon, David
dc.contributor.authorRocha, Eduardo P.C.
dc.date.accessioned2020-12-10T05:08:30Z
dc.date.available2020-12-10T05:08:30Z
dc.date.issued2020
dc.date.updated2020-07-19T08:33:59Z
dc.description.abstractEscherichia coli is mostly a commensal of birds and mammals, including humans, where it can act as an opportunistic pathogen. It is also found in water and sediments. We investigated the phylogeny, genetic diversification, and habitat-association of 1,294 isolates representative of the phylogenetic diversity of more than 5,000 isolates from the Australian continent. Since many previous studies focused on clinical isolates, we investigated mostly other isolates originating from humans, poultry, wild animals and water. These strains represent the species genetic diversity and reveal widespread associations between phylogroups and isolation sources. The analysis of strains from the same sequence types revealed very rapid change of gene repertoires in the very early stages of divergence, driven by the acquisition of many different types of mobile genetic elements. These elements also lead to rapid variations in genome size, even if few of their genes rise to high frequency in the species. Variations in genome size are associated with phylogroup and isolation sources, but the latter determine the number of MGEs, a marker of recent transfer, suggesting that gene flow reinforces the association of certain genetic backgrounds with specific habitats. After a while, the divergence of gene repertoires becomes linear with phylogenetic distance, presumably reflecting the continuous turnover of mobile element and the occasional acquisition of adaptive genes. Surprisingly, the phylogroups with smallest genomes have the highest rates of gene repertoire diversification and fewer but more diverse mobile genetic elements. This suggests that smaller genomes are associated with higher, not lower, turnover of genetic information. Many of these genomes are from freshwater isolates and have peculiar traits, including a specific capsule, suggesting adaptation to this environment. Altogether, these data contribute to explain why epidemiological clones tend to emerge from specific phylogenetic groups in the presence of pervasive horizontal gene transfer across the species.en_AU
dc.description.sponsorship: This work was supported by in-house funding from Pasteur Institute and the CNRS (M.T., A.P., JAM.S. and EPC.R.) and was partially supported by grants from the Fondation pour la Recherche Me´dicale (https://www.frm.org/) [Equipe FRM 2016, grant DEQ20161136698 to E. D., and Equipe FRM: EQU201903007835 to EPC. R.], by the Laboratoire d’Excellence IBEID (https:// research.pasteur.fr/fr/program_project/integrativebiology-of-emerging-infectious-diseases/) [grant ANR-10-LABX-62-IBEID to EPC.R.), by the INCEPTION project (https://research.pasteur.fr/en/ program_project/inception/) [grant PIA/ANR-16- CONV-0005 to EPC.R.] and by an Australian Research Council Linkage Grant [grant LP120100327 to D.G., B.V., S.B.].en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1553-7390en_AU
dc.identifier.urihttp://hdl.handle.net/1885/216797
dc.language.isoen_AUen_AU
dc.provenance© 2020 Touchon et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_AU
dc.publisherPublic Library of Scienceen_AU
dc.relationhttp://purl.org/au-research/grants/arc/LP120100327en_AU
dc.rights© 2020 Touchon et al.en_AU
dc.sourcePLoS Geneticsen_AU
dc.titlePhylogenetic background and habitat drive the genetic diversification of Escherichia colien_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue6en_AU
local.bibliographicCitation.startpagee1008866en_AU
local.contributor.affiliationTouchon, Marie, Institut Pasteuren_AU
local.contributor.affiliationPerrin, Amandine, Institut Pasteuren_AU
local.contributor.affiliationde Sousa, Jorge Andre Moura, Institut Pasteuren_AU
local.contributor.affiliationVangchhia, Belinda, College of Science, ANUen_AU
local.contributor.affiliationBurn, Samantha, College of Science, ANUen_AU
local.contributor.affiliationO'Brien, Claire L., University of Wollongongen_AU
local.contributor.affiliationDenamur, Erick, Universite Parisen_AU
local.contributor.affiliationGordon, David, College of Science, ANUen_AU
local.contributor.affiliationRocha, Eduardo P.C., Institut Pasteuren_AU
local.contributor.authoruidVangchhia, Belinda, u5295100en_AU
local.contributor.authoruidBurn, Samantha, u4212902en_AU
local.contributor.authoruidGordon, David, u9308141en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor060504 - Microbial Ecologyen_AU
local.identifier.absseo970106 - Expanding Knowledge in the Biological Sciencesen_AU
local.identifier.ariespublicationu9511635xPUB2059en_AU
local.identifier.citationvolume16en_AU
local.identifier.doi10.1371/journal.pgen.1008866en_AU
local.publisher.urlhttp://www.plosgenetics.org/en_AU
local.type.statusPublished Versionen_AU

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