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Flexible genes establish widespread bacteriophage pan-genomes in cryoconite hole ecosystems

Author

Listed:
  • Christopher M. Bellas

    (University of Innsbruck)

  • Declan C. Schroeder

    (University of Minnesota
    University of Reading)

  • Arwyn Edwards

    (Aberystwyth University)

  • Gary Barker

    (University of Bristol)

  • Alexandre M. Anesio

    (Aarhus University)

Abstract

Bacteriophage genomes rapidly evolve via mutation and horizontal gene transfer to counter evolving bacterial host defenses; such arms race dynamics should lead to divergence between phages from similar, geographically isolated ecosystems. However, near-identical phage genomes can reoccur over large geographical distances and several years apart, conversely suggesting many are stably maintained. Here, we show that phages with near-identical core genomes in distant, discrete aquatic ecosystems maintain diversity by possession of numerous flexible gene modules, where homologous genes present in the pan-genome interchange to create new phage variants. By repeatedly reconstructing the core and flexible regions of phage genomes from different metagenomes, we show a pool of homologous gene variants co-exist for each module in each location, however, the dominant variant shuffles independently in each module. These results suggest that in a natural community, recombination is the largest contributor to phage diversity, allowing a variety of host recognition receptors and genes to counter bacterial defenses to co-exist for each phage.

Suggested Citation

  • Christopher M. Bellas & Declan C. Schroeder & Arwyn Edwards & Gary Barker & Alexandre M. Anesio, 2020. "Flexible genes establish widespread bacteriophage pan-genomes in cryoconite hole ecosystems," Nature Communications, Nature, vol. 11(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-18236-8
    DOI: 10.1038/s41467-020-18236-8
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    Cited by:

    1. Susheel Bhanu Busi & Massimo Bourquin & Stilianos Fodelianakis & Grégoire Michoud & Tyler J. Kohler & Hannes Peter & Paraskevi Pramateftaki & Michail Styllas & Matteo Tolosano & Vincent Staercke & Mar, 2022. "Genomic and metabolic adaptations of biofilms to ecological windows of opportunity in glacier-fed streams," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    2. Piotr Rozwalak & Jakub Barylski & Yasas Wijesekara & Bas E. Dutilh & Andrzej Zielezinski, 2024. "Ultraconserved bacteriophage genome sequence identified in 1300-year-old human palaeofaeces," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    3. Janina Rahlff & Sarah P. Esser & Julia Plewka & Mara Elena Heinrichs & André Soares & Claudio Scarchilli & Paolo Grigioni & Heike Wex & Helge-Ansgar Giebel & Alexander J. Probst, 2023. "Marine viruses disperse bidirectionally along the natural water cycle," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
    4. Rafael Gonzalez-Serrano & Riccardo Rosselli & Juan J. Roda-Garcia & Ana-Belen Martin-Cuadrado & Francisco Rodriguez-Valera & Matthew Dunne, 2023. "Distantly related Alteromonas bacteriophages share tail fibers exhibiting properties of transient chaperone caps," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    5. Liyun An & Xinwu Liu & Jianwei Wang & Jinbo Xu & Xiaoli Chen & Xiaonan Liu & Bingxin Hu & Yong Nie & Xiao-Lei Wu, 2024. "Global diversity and ecological functions of viruses inhabiting oil reservoirs," Nature Communications, Nature, vol. 15(1), pages 1-16, December.

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