Evidence map›Paper›PMID 32051187›Full record

ArticleGenome research2020

TraDIS-Xpress: a high-resolution whole-genome assay identifies novel mechanisms of triclosan action and resistance.

Muhammad Yasir, A Keith Turner, Sarah Bastkowski, David Baker, Andrew J Page, Andrea Telatin, Minh-Duy Phan, Leigh Monahan, George M Savva, Aaron Darling and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing 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

41 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Tazobactam selects for multidrug resistance.npj antimicrobials and resistance · 2025
    Article
  8. Review
  9. The Secondary Resistome of Methicillin-ResistantAntibiotics (Basel, Switzerland) · 2025
    Article
  10. Article
  11. Review
  12. The Evolution of Next-Generation Sequencing Technologies.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Identification of pathways required forApplied and environmental microbiology · 2024
    Article
  17. Article
  18. Article
  19. Article
  20. Review
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

12 authors at 4 institutions in 2 countries.

Muhammad Yasir *Quadram Institute Bioscience, Norwich Research Park, Norwich, NR4 7UQ, United Kingdom.
A Keith Turner *Quadram Institute Bioscience, Norwich Research Park, Norwich, NR4 7UQ, United Kingdom.
Sarah BastkowskiQuadram Institute Bioscience, Norwich Research Park, Norwich, NR4 7UQ, United Kingdom.ORCID 0000-0001-9002-1822
David BakerQuadram Institute Bioscience, Norwich Research Park, Norwich, NR4 7UQ, United Kingdom.
Andrew J PageQuadram Institute Bioscience, Norwich Research Park, Norwich, NR4 7UQ, United Kingdom.
Andrea TelatinQuadram Institute Bioscience, Norwich Research Park, Norwich, NR4 7UQ, United Kingdom.
Minh-Duy PhanSchool of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia 4072, Queensland, Australia.
Leigh MonahanFaculty of Science, University of Technology Sydney, New South Wales 2007, Australia.
George M SavvaQuadram Institute Bioscience, Norwich Research Park, Norwich, NR4 7UQ, United Kingdom.
Aaron DarlingFaculty of Science, University of Technology Sydney, New South Wales 2007, Australia.
Mark A WebberQuadram Institute Bioscience, Norwich Research Park, Norwich, NR4 7UQ, United Kingdom.
Ian G CharlesQuadram Institute Bioscience, Norwich Research Park, Norwich, NR4 7UQ, United Kingdom.
Norwich Research Park · GBUniversity of East Anglia · GBUniversity of Technology Sydney · AUThe University of Queensland · AU

Funding

Biotechnology and Biological Sciences Research Council BB/CCG1860/1Biotechnology and Biological Sciences Research Council BB/D020476/1Biotechnology and Biological Sciences Research Council BB/G012016/1Biotechnology and Biological Sciences Research Council BB/R012504/1Biotechnology and Biological Sciences Research Council BBS/E/F/000PR10349Medical Research Council MR/L015080/1
6 · The paper itself

Abstract

Understanding the genetic basis for a phenotype is a central goal in biological research. Much has been learnt about bacterial genomes by creating large mutant libraries and looking for conditionally important genes. However, current genome-wide methods are largely unable to assay essential genes which are not amenable to disruption. To overcome this limitation, we developed a new version of "TraDIS" (transposon directed insertion-site sequencing) that we term "TraDIS-Xpress" that combines an inducible promoter into the transposon cassette. This allows controlled overexpression and repression of all genes owing to saturation of inserts adjacent to all open reading frames as well as conventional inactivation. We applied TraDIS-Xpress to identify responses to the biocide triclosan across a range of concentrations. Triclosan is endemic in modern life, but there is uncertainty about its mode of action with a concentration-dependent switch from bacteriostatic to bactericidal action unexplained. Our results show a concentration-dependent response to triclosan with different genes important in survival between static and cidal exposures. These genes include those previously reported to have a role in triclosan resistance as well as a new set of genes, including essential genes. Novel genes identified as being sensitive to triclosan exposure include those involved in barrier function, small molecule uptake, and integrity of transcription and translation. We anticipate the approach we show here, by allowing comparisons across multiple experimental conditions of TraDIS data, and including essential genes, will be a starting point for future work examining how different drug conditions impact bacterial survival mechanisms.

Indexed as

DNA Transposable ElementsEscherichia coliGene LibraryGenes, EssentialGenome, BacterialMutagenesis, InsertionalMutant ProteinsPhenotypeTriclosanDNA Transposable ElementsMutant ProteinsTriclosan

Identifiers

PMID32051187
PMCPMC7050523
OpenAlexW3006301344

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.