Evidence map›Paper›PMID 37267422›Full record

ArticlePLoS pathogens2023

Targeted IS-element sequencing uncovers transposition dynamics during selective pressure in enterococci.

Joshua M Kirsch, Shannon Ely, Madison E Stellfox, Karthik Hullahalli, Phat Luong, Kelli L Palmer, Daria Van Tyne, Breck A Duerkop

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.5field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

18 citing papers in PubMed, 22 citations in OpenAlex.

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  11. Local Genomic Surveillance of InvasiveInternational journal of molecular sciences · 2024
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  17. Genome reduction inFrontiers in bioengineering and biotechnology · 2024
    Article
  18. Article
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

8 authors at 3 institutions in 1 country.

Joshua M KirschDepartment of Immunology and Microbiology, University of Colorado-Anschutz Medical Campus, School of Medicine, Aurora, Colorado, United States of America.
Shannon ElyDepartment of Immunology and Microbiology, University of Colorado-Anschutz Medical Campus, School of Medicine, Aurora, Colorado, United States of America.
Madison E StellfoxDepartment of Medicine, Division of Infectious Diseases, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Karthik HullahalliDepartment of Biological Sciences, University of Texas at Dallas, Richardson, Texas, United States of America.
Phat LuongDepartment of Immunology and Microbiology, University of Colorado-Anschutz Medical Campus, School of Medicine, Aurora, Colorado, United States of America.
Kelli L PalmerDepartment of Biological Sciences, University of Texas at Dallas, Richardson, Texas, United States of America.
Daria Van TyneDepartment of Medicine, Division of Infectious Diseases, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Breck A DuerkopDepartment of Immunology and Microbiology, University of Colorado-Anschutz Medical Campus, School of Medicine, Aurora, Colorado, United States of America.ORCID 0000-0003-4030-9822
University of Colorado Anschutz Medical Campus · USThe University of Texas at Dallas · USUniversity of Pittsburgh · US

Funding

Mechanistic basis of bacteriophages for the decolonization of vancomycin resistant enterococci in the intestine.R01AI141479 · NIAID · UNIVERSITY OF COLORADO DENVER · PI DUERKOP, BRECK A · 2018 to 2025
$4.4M
Adaptation of vancomycin-resistant enterococci during bloodstream infectionR01AI165519 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VAN TYNE, DARIA N · 2022 to 2025
$3.0M
Molecular Pathogenesis of Infectious DiseasesT32AI052066 · NIAID · UNIVERSITY OF COLORADO DENVER · PI VAN DYK, LINDA F. · 2002 to 2022
$2.3M
Genome defense and acquired antibiotic resistance in Enterococcus faecalis and Enterococcus faeciumR01AI116610 · NIAID · UNIVERSITY OF TEXAS DALLAS · PI PALMER, KELLI LEA · 2015 to 2019
$1.9M
University of Pittsburgh Training Program in Antimicrobial ResistanceT32AI138954 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HARRISON, LEE H · 2019 to 2023
$971k
Expansion of enterococcal insertion sequence elements during bacteriophage infectionF31AI169976 · NIAID · UNIVERSITY OF COLORADO DENVER · PI KIRSCH, JOSHUA M · 2022 to 2023
$69k
NIAID NIH HHS F31 AI169976NIAID NIH HHS R01 AI116610NIAID NIH HHS R01 AI141479NIAID NIH HHS R01 AI165519NIAID NIH HHS T32 AI052066NIAID NIH HHS T32 AI138954
6 · The paper itself

Abstract

Insertion sequences (IS) are simple transposons implicated in the genome evolution of diverse pathogenic bacterial species. Enterococci have emerged as important human intestinal pathogens with newly adapted virulence potential and antibiotic resistance. These genetic features arose in tandem with large-scale genome evolution mediated by mobile elements. Pathoadaptation in enterococci is thought to be mediated in part by the IS element IS256 through gene inactivation and recombination events. However, the regulation of IS256 and the mechanisms controlling its activation are not well understood. Here, we adapt an IS256-specfic deep sequencing method to describe how chronic lytic phage infection drives widespread diversification of IS256 in E. faecalis and how antibiotic exposure is associated with IS256 diversification in E. faecium during a clinical human infection. We show through comparative genomics that IS256 is primarily found in hospital-adapted enterococcal isolates. Analyses of IS256 transposase gene levels reveal that IS256 mobility is regulated at the transcriptional level by multiple mechanisms in E. faecalis, indicating tight control of IS256 activation in the absence of selective pressure. Our findings reveal that stressors such as phages and antibiotic exposure drives rapid genome-scale transposition in the enterococci. IS256 diversification can therefore explain how selective pressures mediate evolution of the enterococcal genome, ultimately leading to the emergence of dominant nosocomial lineages that threaten human health.

Indexed as

EnterococcusEnterococcus faeciumAnti-Bacterial AgentsDNA Transposable ElementsDrug Resistance, MicrobialEnterococcus faecalisHumansAnti-Bacterial AgentsDNA Transposable Elements

Identifiers

PMID37267422
PMCPMC10266640
OpenAlexW4379184506

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.