Evidence map›Paper›PMID 34606604›Full record

ArticleNucleic acids research2022

CRISPR-Cas systems are widespread accessory elements across bacterial and archaeal plasmids.

Rafael Pinilla-Redondo, Jakob Russel, David Mayo-Muñoz, Shiraz A Shah, Roger A Garrett, Joseph Nesme, Jonas S Madsen, Peter C Fineran, Søren J Sørensen

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
5.8field-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

63 citing papers in PubMed, 104 citations in OpenAlex.

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  6. Hawaiian Geothermal Fumaroles Contain Diverse and Novel Viruses.bioRxiv : the preprint server for biology · 2026
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  11. [Research on Bacteriophage Resistance: Coevolutionary Arms Race Between Bacteria and Phages Drives Novel Antibacterial Therapies].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2026
    Review
  12. Review
  13. Article
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  16. Article
  17. Article
  18. The H-NS homologues MvaT and MvaU repress CRISPR-Cas inPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Article
  19. Article
  20. Review

3 more citing papers are in PubMed but not listed here.

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

9 authors at 2 institutions in 2 countries.

Rafael Pinilla-RedondoSection of Microbiology, University of Copenhagen, Universitetsparken 15, 2100 Copenhagen, Denmark.ORCID 0000-0003-3521-460X
Jakob RusselSection of Microbiology, University of Copenhagen, Universitetsparken 15, 2100 Copenhagen, Denmark.ORCID 0000-0002-0565-3161
David Mayo-MuñozSection of Microbiology, University of Copenhagen, Universitetsparken 15, 2100 Copenhagen, Denmark.ORCID 0000-0003-0751-4787
Shiraz A ShahCopenhagen Prospective Studies on Asthma in Childhood (COPSAC), Herlev and Gentofte Hospital, University of Copenhagen, Ledreborg Alle 34, 2820 Gentofte, Denmark.
Roger A GarrettDanish Archaea Centre, Department of Biology, University of Copenhagen, University of Copenhagen, Ole Maaløes Vej 5, 2200 Copenhagen, Denmark.
Joseph NesmeSection of Microbiology, University of Copenhagen, Universitetsparken 15, 2100 Copenhagen, Denmark.ORCID 0000-0003-1929-5040
Jonas S MadsenSection of Microbiology, University of Copenhagen, Universitetsparken 15, 2100 Copenhagen, Denmark.
Peter C FineranDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.ORCID 0000-0002-4639-6704
Søren J SørensenSection of Microbiology, University of Copenhagen, Universitetsparken 15, 2100 Copenhagen, Denmark.ORCID 0000-0001-6227-9906
University of Copenhagen · DKUniversity of Otago · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many prokaryotes encode CRISPR-Cas systems as immune protection against mobile genetic elements (MGEs), yet a number of MGEs also harbor CRISPR-Cas components. With a few exceptions, CRISPR-Cas loci encoded on MGEs are uncharted and a comprehensive analysis of their distribution, prevalence, diversity, and function is lacking. Here, we systematically investigated CRISPR-Cas loci across the largest curated collection of natural bacterial and archaeal plasmids. CRISPR-Cas loci are widely but heterogeneously distributed across plasmids and, in comparison to host chromosomes, their mean prevalence per Mbp is higher and their distribution is distinct. Furthermore, the spacer content of plasmid CRISPRs exhibits a strong targeting bias towards other plasmids, while chromosomal arrays are enriched with virus-targeting spacers. These contrasting targeting preferences highlight the genetic independence of plasmids and suggest a major role for mediating plasmid-plasmid conflicts. Altogether, CRISPR-Cas are frequent accessory components of many plasmids, which is an overlooked phenomenon that possibly facilitates their dissemination across microbiomes.

Indexed as

ArchaeaCRISPR-Cas SystemsBacteriaPlasmidsProkaryotic Cells

Identifiers

PMID34606604
PMCPMC9071438
OpenAlexW3204800826

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.