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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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 Creators:
Backman, T, Author
Latorre, SM1, 2, Author                 
Symeonidi, E, Author                 
Muszyński, A, Author
Bleak , E, Author
Eads, L, Author
Martinez-Koury, PI, Author
Som, S, Author
Hawks, A, Author
Gloss, AD, Author
Belnap, DM, Author
Manuel, AM, Author
Deutschbauer, AM, Author
Bergelson, J, Author
Azadi, P, Author
Burbano, HA1, 2, Author                 
Karasov, TL, Author                 
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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 Abstract: 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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 Dates: 2024-06
 Publication Status: Issued
 Pages: -
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 Rev. Type: -
 Identifiers: DOI: 10.1126/science.ado0713
PMID: 38870284
 Degree: -

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Title: Science
  Abbreviation : Science
Source Genre: Journal
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Publ. Info: Washington, D.C. : American Association for the Advancement of Science
Pages: 14 Volume / Issue: 384 (6701) Sequence Number: eado0713 Start / End Page: - Identifier: ISSN: 0036-8075
CoNE: https://pure.mpg.de/cone/journals/resource/991042748276600_1