Evidence map›Paper›PMID 32732904›Full record

ArticleThe ISME journal2020

Modular prophage interactions driven by capsule serotype select for capsule loss under phage predation.

Jorge A M de Sousa, Amandine Buffet, Matthieu Haudiquet, Eduardo P C Rocha, Olaya Rendueles

Open access · hybridAbstract read
In one paragraph

Article in The ISME journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
7.1field-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

46 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. The Potential Roles of Prophages in the Pathogenicity ofAntibiotics (Basel, Switzerland) · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. The extended mobility of plasmids.Nucleic acids research · 2025
    Review
  12. Review
  13. mBio · 2025
    Article
  14. Article
  15. Viruses · 2025
    Article
  16. Review
  17. Article
  18. Article
  19. Targeted phage hunting to specificMicrobiology spectrum · 2024
    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

5 authors at 1 institution in 2 countries.

Jorge A M de SousaMicrobial Evolutionary Genomics, Institut Pasteur, CNRS, UMR3525, Paris, 75015, France.
Amandine BuffetMicrobial Evolutionary Genomics, Institut Pasteur, CNRS, UMR3525, Paris, 75015, France.
Matthieu HaudiquetMicrobial Evolutionary Genomics, Institut Pasteur, CNRS, UMR3525, Paris, 75015, France.ORCID http://orcid.org/0000-0002-0878-2209
Eduardo P C RochaMicrobial Evolutionary Genomics, Institut Pasteur, CNRS, UMR3525, Paris, 75015, France.ORCID http://orcid.org/0000-0001-7704-822X
Olaya RenduelesMicrobial Evolutionary Genomics, Institut Pasteur, CNRS, UMR3525, Paris, 75015, France. olaya.rendueles-garcia@pasteur.fr.ORCID http://orcid.org/0000-0002-6648-1594
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Klebsiella species are able to colonize a wide range of environments and include worrisome nosocomial pathogens. Here, we sought to determine the abundance and infectivity of prophages of Klebsiella to understand how the interactions between induced prophages and bacteria affect population dynamics and evolution. We identified many prophages in the species, placing these taxa among the top 5% of the most polylysogenic bacteria. We selected 35 representative strains of the Klebsiella pneumoniae species complex to establish a network of induced phage-bacteria interactions. This revealed that many prophages are able to enter the lytic cycle, and subsequently kill or lysogenize closely related Klebsiella strains. Although 60% of the tested strains could produce phages that infect at least one other strain, the interaction network of all pairwise cross-infections is very sparse and mostly organized in modules corresponding to the strains' capsule serotypes. Accordingly, capsule mutants remain uninfected showing that the capsule is a key factor for successful infections. Surprisingly, experiments in which bacteria are predated by their own prophages result in accelerated loss of the capsule. Our results show that phage infectiousness defines interaction modules between small subsets of phages and bacteria in function of capsule serotype. This limits the role of prophages as competitive weapons because they can infect very few strains of the species complex. This should also restrict phage-driven gene flow across the species. Finally, the accelerated loss of the capsule in bacteria being predated by their own phages, suggests that phages drive serotype switch in nature.

Indexed as

BacteriophagesProphagesAnimalsBacteriaPredatory BehaviorSerogroup

Identifiers

PMID32732904
PMCPMC7784688
OpenAlexW3045871637

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.