Evidence map›Paper›PMID 36669116›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Antibiotics that affect translation can antagonize phage infectivity by interfering with the deployment of counter-defenses.

Benoit J Pons, Tatiana Dimitriu, Edze R Westra, Stineke van Houte

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Phage susceptibility to a minimal, modular synthetic CRISPR-Cas system inPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Phage-antibiotic combinations againstFrontiers in microbiology · 2025
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. 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

4 authors at 1 institution in 1 country.

Benoit J PonsEnvironment and Sustainability Institute, Biosciences, University of Exeter, Penryn TR10 9FE, UK.ORCID 0000-0002-9137-1047
Tatiana DimitriuEnvironment and Sustainability Institute, Biosciences, University of Exeter, Penryn TR10 9FE, UK.
Edze R WestraEnvironment and Sustainability Institute, Biosciences, University of Exeter, Penryn TR10 9FE, UK.ORCID 0000-0003-4396-0354
Stineke van HouteEnvironment and Sustainability Institute, Biosciences, University of Exeter, Penryn TR10 9FE, UK.
University of Exeter · GB

Funding

EC | ERC | HORIZON EUROPE European Research Council (ERC) ERC-STG-2016-714478European Research CouncilUKRI | Biotechnology and Biological Sciences Research Council (BBSRC) BB/R010781/1UKRI | Biotechnology and Biological Sciences Research Council (BBSRC) BB/S017674/1UKRI | Engineering and Physical Sciences Research Council (EPSRC) EP/X026507/1
6 · The paper itself

Abstract

It is becoming increasingly clear that antibiotics can both positively and negatively impact the infectivity of bacteriophages (phage), but the underlying mechanisms often remain unclear. Here we demonstrate that antibiotics that target the protein translation machinery can fundamentally alter the outcome of bacteria-phage interactions by interfering with the production of phage-encoded counter-defense proteins. Specifically, using Pseudomonas aeruginosa PA14 and phage DMS3vir as a model, we show that bacteria with Clustered Regularly Interspaced Short Palindromic Repeat, CRISPR associated (CRISPR-Cas) immune systems have elevated levels of immunity against phage that encode anti-CRISPR (acr) genes when translation inhibitors are present in the environment. CRISPR-Cas are highly prevalent defense systems that enable bacteria to detect and destroy phage genomes in a sequence-specific manner. In response, many phages encode

Indexed as

BacteriophagesCRISPR-Cas SystemsAnti-Bacterial AgentsBacteriaViral ProteinsAnti-Bacterial AgentsViral Proteinsantibioticsanti-CRISPRbacteriophageCRISPR-Castranslation inhibitors

Identifiers

PMID36669116
PMCPMC9942909
OpenAlexW4317566706

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.