Evolution of the pheV-tRNA integrated genomic island in Escherichia coli.


Journal

PLoS genetics
ISSN: 1553-7404
Titre abrégé: PLoS Genet
Pays: United States
ID NLM: 101239074

Informations de publication

Date de publication:
24 Oct 2024
Historique:
received: 12 05 2024
accepted: 14 10 2024
medline: 25 10 2024
pubmed: 25 10 2024
entrez: 24 10 2024
Statut: aheadofprint

Résumé

Escherichia coli exhibit extensive genetic diversity at the genome level, particularly within their accessory genome. The tRNA integrated genomic islands (GIs), a part of the E. coli accessory genome, play an important role in pathogenicity. However, studies examining the evolution of GIs have been challenging due to their large size, considerable gene content variation and fragmented assembly in draft genomes. Here we examined the evolution of the GI integrated at pheV-tRNA (GI-pheV), with a primary focus on uropathogenic E. coli (UPEC) and the globally disseminated multidrug resistant ST131 clone. We show the gene content of GI-pheV is highly diverse and arranged in a modular configuration, with the P4 integrase encoding gene intP4 the only conserved gene. Despite this diversity, the GI-pheV gene content displayed conserved features among strains from the same pathotype. In ST131, GI-pheV corresponding to the reference strain EC958 (EC958_GI-pheV) was found in ~90% of strains. Phylogenetic analyses suggested that GI-pheV in ST131 has evolved together with the core genome, with the loss/gain of specific modules (or the entire GI) linked to strain specific events. Overall, we show GI-pheV exhibits a dynamic evolutionary pathway, in which modules and genes have evolved through multiple events including insertions, deletions and recombination.

Identifiants

pubmed: 39446883
doi: 10.1371/journal.pgen.1011459
pii: PGENETICS-D-24-00527
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1011459

Informations de copyright

Copyright: © 2024 Nhu 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.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Nguyen Thi Khanh Nhu (NTK)

Institute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Queensland, Australia.
Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Queensland, Australia.

Brian M Forde (BM)

Institute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Queensland, Australia.
Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Queensland, Australia.
UQ Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.

Nouri L Ben Zakour (NL)

School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Queensland, Australia.

Minh-Duy Phan (MD)

Institute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Queensland, Australia.
Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Queensland, Australia.

Leah W Roberts (LW)

UQ Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.

Scott A Beatson (SA)

Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Queensland, Australia.
School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Queensland, Australia.

Mark A Schembri (MA)

Institute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Queensland, Australia.
Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Queensland, Australia.
School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Queensland, Australia.

Classifications MeSH