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  A phage tail-like bacteriocin suppresses competitors in metapopulations of pathogenic bacteria

Backman, T., Latorre, S., Symeonidi, E., Muszyński, A., Bleak, E., Eads, L., et al. (2024). A phage tail-like bacteriocin suppresses competitors in metapopulations of pathogenic bacteria. Science, 384(6701): eado0713. doi:10.1126/science.ado0713.

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Backman, T, Autor
Latorre, SM1, 2, Autor                 
Symeonidi, E, Autor                 
Muszyński, A, Autor
Bleak , E, Autor
Eads, L, Autor
Martinez-Koury, PI, Autor
Som, S, Autor
Hawks, A, Autor
Gloss, AD, Autor
Belnap, DM, Autor
Manuel, AM, Autor
Deutschbauer, AM, Autor
Bergelson, J, Autor
Azadi, P, Autor
Burbano, HA1, 2, Autor                 
Karasov, TL, Autor                 
Affiliations:
1Department Molecular Biology, Max Planck Institute for Biology Tübingen, Max Planck Society, ou_3371687              
2Research Group for Ancient Genomics and Evolution, Department Molecular Biology, Max Planck Institute for Biology Tübingen, Max Planck Society, ou_3593983              

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 Zusammenfassung: Bacteria can repurpose their own bacteriophage viruses (phage) to kill competing bacteria. Phage-derived elements are frequently strain specific in their killing activity, although there is limited evidence that this specificity drives bacterial population dynamics. Here, we identified intact phage and their derived elements in a metapopulation of wild plant-associated Pseudomonas genomes. We discovered that the most abundant viral cluster encodes a phage remnant resembling a phage tail called a tailocin, which bacteria have co-opted to kill bacterial competitors. Each pathogenic Pseudomonas strain carries one of a few distinct tailocin variants that target the variable polysaccharides in the outer membrane of co-occurring pathogenic Pseudomonas strains. Analysis of herbarium samples from the past 170 years revealed that the same tailocin and bacterial receptor variants have persisted in Pseudomonas populations. These results suggest that tailocin genetic diversity can be mined to develop targeted "tailocin cocktails" for microbial control.

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 Datum: 2024-06
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
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 Identifikatoren: DOI: 10.1126/science.ado0713
PMID: 38870284
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Titel: Science
  Kurztitel : Science
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Washington, D.C. : American Association for the Advancement of Science
Seiten: 14 Band / Heft: 384 (6701) Artikelnummer: eado0713 Start- / Endseite: - Identifikator: ISSN: 0036-8075
CoNE: https://pure.mpg.de/cone/journals/resource/991042748276600_1