Evidence map›Paper›PMID 39401066›Full record

ArticleMicrobial genomics2024

Applying rearrangement distances to enable plasmid epidemiology with pling.

Daria Frolova, Leandro Lima, Leah Wendy Roberts, Leonard Bohnenkämper, Roland Wittler, Jens Stoye, Zamin Iqbal

Abstract read
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Article in Microbial genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact
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

37 citing papers in PubMed.

  1. Article
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  13. A One Health study ofMicrobial genomics · 2026
    Article
  14. Article
  15. Article
  16. Article
  17. Genomic characterization ofApplied and environmental microbiology · 2025
    Article
  18. Review
  19. Genomic Characterization of NDM-1 ProducerAntibiotics (Basel, Switzerland) · 2025
    Article
  20. 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

7 authors.

Daria FrolovaEuropean Bioinformatics Institute, Hinxton, Cambridge CB10 1SD, UK.
Leandro LimaEuropean Bioinformatics Institute, Hinxton, Cambridge CB10 1SD, UK.
Leah Wendy RobertsCentre for Immunology and Infection Control, Queensland University of Technology, Brisbane, Queensland, Australia.
Leonard BohnenkämperFaculty of Technology and Center for Biotechnology (CeBiTec), Bielefeld University, Bielefeld, Germany.
Roland WittlerFaculty of Technology and Center for Biotechnology (CeBiTec), Bielefeld University, Bielefeld, Germany.
Jens StoyeFaculty of Technology and Center for Biotechnology (CeBiTec), Bielefeld University, Bielefeld, Germany.
Zamin IqbalEuropean Bioinformatics Institute, Hinxton, Cambridge CB10 1SD, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasmids are a key vector of antibiotic resistance, but the current bioinformatics toolkit is not well suited to tracking them. The rapid structural changes seen in plasmid genomes present considerable challenges to evolutionary and epidemiological analysis. Typical approaches are either low resolution (replicon typing) or use shared k-mer content to define a genetic distance. However, this distance can both overestimate plasmid relatedness by ignoring rearrangements, and underestimate by over-penalizing gene gain/loss. Therefore a model is needed which captures the key components of how plasmid genomes evolve structurally - through gene/block gain or loss, and rearrangement. A secondary requirement is to prevent promiscuous transposable elements (TEs) leading to over-clustering of unrelated plasmids. We choose the 'Double Cut and Join Indel' (DCJ-Indel) model, in which plasmids are studied at a coarse level, as a sequence of signed integers (representing genes or aligned blocks), and the distance between two plasmids is the minimum number of rearrangement events or indels needed to transform one into the other. We show how this gives much more meaningful distances between plasmids. We introduce a software workflow pling (https://github.com/iqbal-lab-org/pling), which uses the DCJ-Indel model, to calculate distances between plasmids and then cluster them. In our approach, we combine containment distances and DCJ-Indel distances to build a TE-aware plasmid network. We demonstrate superior performance and interpretability to other plasmid clustering tools on the 'Russian Doll' dataset and a hospital transmission dataset.

Indexed as

PlasmidsSoftwareComputational BiologyDNA Transposable ElementsEvolution, MolecularGene RearrangementHumansINDEL MutationDNA Transposable Elementsclusteringmobile genetic elementsplasmidsrearrangementstransmissionwhole genome analysis

Identifiers

PMID39401066
PMCPMC11472880

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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.