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Numerous cultivated and uncultivated viruses encode ribosomal proteins

Author

Listed:
  • Carolina M. Mizuno

    (Institut Pasteur)

  • Charlotte Guyomar

    (Univ Rennes, CNRS, IGDR (Institut de génétique et développement de Rennes) - UMR 6290)

  • Simon Roux

    (Department of Energy Joint Genome Institute)

  • Régis Lavigne

    (PROTIM)

  • Francisco Rodriguez-Valera

    (Universidad Miguel Hernandez)

  • Matthew B. Sullivan

    (The Ohio State University
    The Ohio State University)

  • Reynald Gillet

    (Univ Rennes, CNRS, IGDR (Institut de génétique et développement de Rennes) - UMR 6290)

  • Patrick Forterre

    (Institut Pasteur)

  • Mart Krupovic

    (Institut Pasteur)

Abstract

Viruses modulate ecosystems by directly altering host metabolisms through auxiliary metabolic genes. However, viral genomes are not known to encode the core components of translation machinery, such as ribosomal proteins (RPs). Here, using reference genomes and global-scale viral metagenomic datasets, we identify 14 different RPs across viral genomes arising from cultivated viral isolates and metagenome-assembled viruses. Viruses tend to encode dynamic RPs, easily exchangeable between ribosomes, suggesting these proteins can replace cellular versions in host ribosomes. Functional assays confirm that the two most common virus-encoded RPs, bS21 and bL12, are incorporated into 70S ribosomes when expressed in Escherichia coli. Ecological distribution of virus-encoded RPs suggests some level of ecosystem adaptations as aquatic viruses and viruses of animal-associated bacteria are enriched for different subsets of RPs. Finally, RP genes are under purifying selection and thus likely retained an important function after being horizontally transferred into virus genomes.

Suggested Citation

  • Carolina M. Mizuno & Charlotte Guyomar & Simon Roux & Régis Lavigne & Francisco Rodriguez-Valera & Matthew B. Sullivan & Reynald Gillet & Patrick Forterre & Mart Krupovic, 2019. "Numerous cultivated and uncultivated viruses encode ribosomal proteins," Nature Communications, Nature, vol. 10(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-08672-6
    DOI: 10.1038/s41467-019-08672-6
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    Cited by:

    1. Zhirui Cao & Dejun Fan & Yang Sun & Ziyu Huang & Yue Li & Runping Su & Feng Zhang & Qing Li & Hongju Yang & Fen Zhang & Yinglei Miao & Ping Lan & Xiaojian Wu & Tao Zuo, 2024. "The gut ileal mucosal virome is disturbed in patients with Crohn’s disease and exacerbates intestinal inflammation in mice," Nature Communications, Nature, vol. 15(1), pages 1-22, December.
    2. Zihao Zhao & Chie Amano & Thomas Reinthaler & Federico Baltar & Mónica V. Orellana & Gerhard J. Herndl, 2024. "Metaproteomic analysis decodes trophic interactions of microorganisms in the dark ocean," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    3. Tony Z. Jia & Yutetsu Kuruma, 2019. "Recent Advances in Origins of Life Research by Biophysicists in Japan," Challenges, MDPI, vol. 10(1), pages 1-21, April.

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