Evidence map›Paper›PMID 31077304›Full record

ReviewFEMS microbiology letters2019

Keeping crispr in check: diverse mechanisms of phage-encoded anti-crisprs.

Despoina Trasanidou, Ana Sousa Gerós, Prarthana Mohanraju, Anna Cornelia Nieuwenweg, Franklin L Nobrega, Raymond H J Staals

Open access · hybridAbstract readReview
In one paragraph

Review in FEMS microbiology letters, 2019. 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
5.3field-weighted citation impact, top 3% 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

41 citing papers in PubMed, 85 citations in OpenAlex.

  1. Bacterial immune systems.Antonie van Leeuwenhoek · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Antibiotics that affect translation can antagonize phage infectivity by interfering with the deployment of counter-defenses.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. Article
  13. Viral Complexity.Biomolecules · 2022
    Review
  14. Article
  15. Review
  16. Article
  17. Targeting Cancer with CRISPR/Cas9-Based Therapy.International journal of molecular sciences · 2022
    Review
  18. Article
  19. Review of CRISPR-Cas Systems inInternational journal of microbiology · 2022
    Review
  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

6 authors at 2 institutions in 1 country.

Despoina TrasanidouLaboratory of Microbiology, Department of Agrotechnology and Food Sciences, Wageningen University and Research, Stippeneng 4, Wageningen 6708 WE, The Netherlands.
Ana Sousa GerósKavli Institute of Nanoscience, Department of Bionanoscience, Delft University of Technology, Van der Maasweg 9, 2629 HZ Delft, The Netherlands.
Prarthana MohanrajuLaboratory of Microbiology, Department of Agrotechnology and Food Sciences, Wageningen University and Research, Stippeneng 4, Wageningen 6708 WE, The Netherlands.
Anna Cornelia NieuwenwegLaboratory of Microbiology, Department of Agrotechnology and Food Sciences, Wageningen University and Research, Stippeneng 4, Wageningen 6708 WE, The Netherlands.
Franklin L NobregaKavli Institute of Nanoscience, Department of Bionanoscience, Delft University of Technology, Van der Maasweg 9, 2629 HZ Delft, The Netherlands.
Raymond H J StaalsLaboratory of Microbiology, Department of Agrotechnology and Food Sciences, Wageningen University and Research, Stippeneng 4, Wageningen 6708 WE, The Netherlands.
Wageningen University & Research · NLDelft University of Technology · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CRISPR-Cas represents the only adaptive immune system of prokaryotes known to date. These immune systems are widespread among bacteria and archaea, and provide protection against invasion of mobile genetic elements, such as bacteriophages and plasmids. As a result of the arms-race between phages and their prokaryotic hosts, phages have evolved inhibitors known as anti-CRISPR (Acr) proteins to evade CRISPR immunity. In the recent years, several Acr proteins have been described in both temperate and virulent phages targeting diverse CRISPR-Cas systems. Here, we describe the strategies of Acr discovery and the multiple molecular mechanisms by which these proteins operate to inhibit CRISPR immunity. We discuss the biological relevance of Acr proteins and speculate on the implications of their activity for the development of improved CRISPR-based research and biotechnological tools.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsEvolution, MolecularBacteriaBacteriophagesCRISPR-Cas SystemsGene EditingHost-Pathogen InteractionsViral ProteinsViral Proteinsanti-crisprcrispr-casgenome editingphage

Identifiers

PMID31077304
PMCPMC6538845
OpenAlexW2944743307

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.