Evidence map›Paper›PMID 41000832›Full record

ArticlebioRxiv : the preprint server for biology2025

YprA family helicases provide the missing link between diverse prokaryotic immune systems.

Ryan T Bell, Thomas Gaudin, Yi Wu, Sofya K Garushyants, Harutyun Sahakyan, Kira S Makarova, Yuri I Wolf, Simon A Jackson, Franklin L Nobrega, Chase L Beisel and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Ryan T BellDivision of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, United States.
Thomas GaudinHelmholtz Institute for RNA-based Infection Research (HIRI), Helmholtz Centre for Infection Research (HZI), 97080 Würzburg, Germany.
Yi WuSchool of Biological Sciences, University of Southampton, SO17 1BJ Southampton, UK.
Sofya K GarushyantsDivision of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, United States.
Harutyun SahakyanDivision of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, United States.
Kira S MakarovaDivision of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, United States.
Yuri I WolfDivision of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, United States.
Simon A JacksonSchool of Pharmacy and Biomedical Sciences, Division of Health, University of Waikato, Hamilton 3126, New Zealand.
Franklin L NobregaSchool of Biological Sciences, University of Southampton, SO17 1BJ Southampton, UK.ORCID 0000-0002-8238-1083
Chase L BeiselHelmholtz Institute for RNA-based Infection Research (HIRI), Helmholtz Centre for Infection Research (HZI), 97080 Würzburg, Germany.ORCID 0000-0003-0650-9943
Eugene V KooninDivision of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, United States.ORCID 0000-0003-3943-8299

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacteria and archaea possess an enormous variety of antivirus immune systems that often share homologous proteins and domains, some of which contribute to diverse defense strategies. YprA family helicases are central to widespread defense systems DISARM, Dpd, and Druantia. Here, through comprehensive phylogenetic and structural prediction analysis of the YprA family, we identify several major, previously unrecognized clades, with unique signatures of domain architecture and associations with other genes. Each YprA family clade defines a distinct class of defense systems, which we denote ARMADA (disARM-related Antiviral Defense Array), BRIGADE (Base hypermodification and Restriction Involving Genes encoding ARMADA-like and Dpd-like Effectors), or TALON (TOTE-like and ARMADA-Like Operon with Nuclease). In addition to the YprA-like helicase, ARMADA systems share two more proteins with DISARM. However, ARMADA YprA homologs are most similar to those of Druantia, suggesting ARMADA is a 'missing link' connecting DISARM and Druantia. We show experimentally that ARMADA protects bacteria against a broad range of phages via a direct, non-abortive mechanism. We also discovered multiple families of satellite phage-like mobile genetic elements that often carry both ARMADA and Druantia Type III systems and show that these can provide synergistic resistance against diverse phages.

Identifiers

PMID41000832
PMCPMC12458937

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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.