Evidence map›Paper›PMID 39446883›Full record

ArticlePLoS genetics2024

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

Nguyen Thi Khanh Nhu, Brian M Forde, Nouri L Ben Zakour, Minh-Duy Phan, Leah W Roberts, Scott A Beatson, Mark A Schembri

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Article in PLoS genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Nguyen Thi Khanh NhuInstitute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Queensland, Australia.ORCID https://orcid.org/0000-0002-0158-850X
Brian M FordeInstitute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Queensland, Australia.ORCID https://orcid.org/0000-0002-2264-4785
Nouri L Ben ZakourSchool of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Queensland, Australia.ORCID https://orcid.org/0000-0002-6949-1755
Minh-Duy PhanInstitute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Queensland, Australia.ORCID https://orcid.org/0000-0002-3426-1044
Leah W RobertsUQ Centre for Clinical Research, Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.ORCID https://orcid.org/0000-0002-1024-0564
Scott A BeatsonAustralian Infectious Diseases Research Centre, The University of Queensland, Brisbane, Queensland, Australia.ORCID https://orcid.org/0000-0002-1806-3283
Mark A SchembriInstitute for Molecular Bioscience (IMB), The University of Queensland, Brisbane, Queensland, Australia.ORCID https://orcid.org/0000-0003-4863-9260

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Escherichia coliEvolution, MolecularGenomic IslandsPhylogenyDrug Resistance, Multiple, BacterialGenetic VariationGenome, BacterialRNA, TransferUropathogenic Escherichia coliRNA, Transfer

Identifiers

PMID39446883
PMCPMC11537424

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.