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Paper · 35985290

Bacteriophages benefit from mobilizing pathogenicity islands encoding immune systems against competitors.

Fillol-Salom A and 6 others. Cell, 2022. Cited by 104 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Bacteriophages benefit from mobilizing pathogenicity islands encoding immune systems against competitors. Papers, record 35985290. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/35985290

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Bacteriophages benefit from mobilizing pathogenicity islands encoding immune systems against competitors.
PubMed
Journal
Cell
PubMed
Year
2022
PubMed
Publication types
Journal Article, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
104
iCite
Relative citation ratio, by iCite
7.92
iCite
Revised in PubMed
2026-07-28
PubMed

Authors7

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Fillol-Salom AAlfred
2Rostøl JTJakob T
3Ojiogu ADAdaeze D
4Chen JJohn
5Douce GGill
6Humphrey SSuzanne
7Penadés JRJosé R

Source PubMed

Topics6

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
BacteriophagesMajor topic
Genomic IslandsMajor topic
Bacteria
Gene Transfer, Horizontal
Immune System
Plasmids

Source PubMed

Grants8

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes itAgencyCountryNIH projectStated by
MR/M003876/1Medical Research CouncilUnited KingdomPubMed
MR/V000772/1Medical Research CouncilUnited KingdomPubMed
MR/S00940X/2Medical Research CouncilUnited KingdomPubMed
BB/V002376/1Biotechnology and Biological Sciences Research CouncilUnited KingdomPubMed
MR/S00940X/1Medical Research CouncilUnited KingdomPubMed
BB/N002873/1Biotechnology and Biological Sciences Research CouncilUnited KingdomPubMed
BB/S003835/1Biotechnology and Biological Sciences Research CouncilUnited KingdomPubMed
201531/Z/16/ZWellcome TrustUnited KingdomPubMed

Source PubMed

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections2

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

KindPMIDTitleIn PapersSource
Comment in36,099,898Bacterial immunity: Mobile genetic elements are hotspots for defence systems.https://conductscience.org/library/papers/36099898PubMed
Comment in36,634,621PICI thieves: Molecular piracy and cooperation.https://conductscience.org/library/papers/36634621PubMed

References0

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

None in this release.

Cited by73

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 104 citations.

PMIDTitleJournalYearIn PapersSource
42,797,876Comparative Genomics of the Enterobacter cloacae Mobilome: Prophage Diversity and Anti-Phage Defense Systems in Phage Satellites.Viruses2026https://conductscience.org/library/papers/42797876PubMed
42,755,366Shuttling, swapping, and mixing: the rapid modular evolution of antiviral repertoires in temperate phages and their satellites.Nucleic Acids Res2026https://conductscience.org/library/papers/42755366PubMed
42,672,116Small serine recombinases are markers for antiphage defense system discovery.PLoS Biol2026https://conductscience.org/library/papers/42672116PubMed
42,584,065Dental wastewater reveals a hidden reservoir of oral bacteriophage diversity.Microbiol Spectr2026https://conductscience.org/library/papers/42584065PubMed
42,564,753Phage tail protein methylation enabling the virus to bind to the surface of bacterial cells is vital for progeny infectivity.Cell Insight2026https://conductscience.org/library/papers/42564753PubMed
42,469,821A versatile toolset for Staphylococcus aureus gene inactivation enables testing of anti-phage defense systems in native genetic backgrounds.Microb Cell Fact2026https://conductscience.org/library/papers/42469821PubMed
42,447,023From hijackers to architects: the role of prophages in bacterial genome evolution.J Bacteriol2026https://conductscience.org/library/papers/42447023PubMed
42,353,603Genomic Characterization and Pathogenicity Island Analysis of 17 Mexican Isolates of Corynebacterium pseudotuberculosis biovar ovis.Curr Issues Mol Biol2026https://conductscience.org/library/papers/42353603PubMed
42,283,811Mobile Genetic Elements as Key Drivers of Bacterial Evolution and Adaptation in Agroecosystems.Microb Ecol2026https://conductscience.org/library/papers/42283811PubMed
42,162,416Revisiting the life cycle of temperate phages.Nat Rev Microbiol2026https://conductscience.org/library/papers/42162416PubMed

1 to 10 of 73

See all 73 cited by

Genes0

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

None in this release.

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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