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A highly abundant bacteriophage discovered in the unknown sequences of human faecal metagenomes

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  • Bas E. Dutilh

    (Centre for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud university medical centre, Geert Grooteplein 28, 6525 GA Nijmegen, The Netherlands
    San Diego State University, 5500 Campanile Drive
    San Diego State University, 5500 Campanile Drive
    Institute of Biology, Federal University of Rio de Janeiro, Av. Carlos Chagas Fo. 373, Prédio Anexo ao Bloco A do Centro de Ciências da Saúde, Ilha do Fundão, CEP 21941-902 Rio de Janeiro, Brazil)

  • Noriko Cassman

    (San Diego State University, 5500 Campanile Drive
    Present address: Netherlands Institute of Ecology, Wageningen, The Netherlands)

  • Katelyn McNair

    (San Diego State University, 5500 Campanile Drive)

  • Savannah E. Sanchez

    (San Diego State University, 5500 Campanile Drive)

  • Genivaldo G. Z. Silva

    (Computational Science Research Center, San Diego State University, 5500 Campanile Drive)

  • Lance Boling

    (San Diego State University, 5500 Campanile Drive)

  • Jeremy J. Barr

    (San Diego State University, 5500 Campanile Drive)

  • Daan R. Speth

    (Institute for Water and Wetland Research, Radboud University, Heyendaalseweg 135)

  • Victor Seguritan

    (San Diego State University, 5500 Campanile Drive)

  • Ramy K. Aziz

    (San Diego State University, 5500 Campanile Drive
    Faculty of Pharmacy, Cairo University, Kasr El-Aini Street)

  • Ben Felts

    (San Diego State University, 5500 Campanile Drive)

  • Elizabeth A. Dinsdale

    (San Diego State University, 5500 Campanile Drive
    Computational Science Research Center, San Diego State University, 5500 Campanile Drive)

  • John L. Mokili

    (San Diego State University, 5500 Campanile Drive)

  • Robert A. Edwards

    (San Diego State University, 5500 Campanile Drive
    Institute of Biology, Federal University of Rio de Janeiro, Av. Carlos Chagas Fo. 373, Prédio Anexo ao Bloco A do Centro de Ciências da Saúde, Ilha do Fundão, CEP 21941-902 Rio de Janeiro, Brazil
    Computational Science Research Center, San Diego State University, 5500 Campanile Drive
    Argonne National Laboratory, 9700 S Cass Ave B109)

Abstract

Metagenomics, or sequencing of the genetic material from a complete microbial community, is a promising tool to discover novel microbes and viruses. Viral metagenomes typically contain many unknown sequences. Here we describe the discovery of a previously unidentified bacteriophage present in the majority of published human faecal metagenomes, which we refer to as crAssphage. Its ~97 kbp genome is six times more abundant in publicly available metagenomes than all other known phages together; it comprises up to 90% and 22% of all reads in virus-like particle (VLP)-derived metagenomes and total community metagenomes, respectively; and it totals 1.68% of all human faecal metagenomic sequencing reads in the public databases. The majority of crAssphage-encoded proteins match no known sequences in the database, which is why it was not detected before. Using a new co-occurrence profiling approach, we predict a Bacteroides host for this phage, consistent with Bacteroides-related protein homologues and a unique carbohydrate-binding domain encoded in the phage genome.

Suggested Citation

  • Bas E. Dutilh & Noriko Cassman & Katelyn McNair & Savannah E. Sanchez & Genivaldo G. Z. Silva & Lance Boling & Jeremy J. Barr & Daan R. Speth & Victor Seguritan & Ramy K. Aziz & Ben Felts & Elizabeth , 2014. "A highly abundant bacteriophage discovered in the unknown sequences of human faecal metagenomes," Nature Communications, Nature, vol. 5(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms5498
    DOI: 10.1038/ncomms5498
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    Cited by:

    1. Joachim Johansen & Damian R. Plichta & Jakob Nybo Nissen & Marie Louise Jespersen & Shiraz A. Shah & Ling Deng & Jakob Stokholm & Hans Bisgaard & Dennis Sandris Nielsen & Søren J. Sørensen & Simon Ras, 2022. "Genome binning of viral entities from bulk metagenomics data," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    2. Javier Lopez-Simon & Marina Vila-Nistal & Aleksandra Rosenova & Daniele Corte & Federico Baltar & Manuel Martinez-Garcia, 2023. "Viruses under the Antarctic Ice Shelf are active and potentially involved in global nutrient cycles," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
    3. Lingling Wang & Haobin Yao & Daniel C. Morgan & Kam Shing Lau & Suet Yi Leung & Joshua W. K. Ho & Wai K. Leung, 2023. "Altered human gut virome in patients undergoing antibiotics therapy for Helicobacter pylori," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
    4. Patrick A. Jonge & Koen Wortelboer & Torsten P. M. Scheithauer & Bert-Jan H. Born & Aeilko H. Zwinderman & Franklin L. Nobrega & Bas E. Dutilh & Max Nieuwdorp & Hilde Herrema, 2022. "Gut virome profiling identifies a widespread bacteriophage family associated with metabolic syndrome," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    5. Suguru Nishijima & Naoyoshi Nagata & Yuya Kiguchi & Yasushi Kojima & Tohru Miyoshi-Akiyama & Moto Kimura & Mitsuru Ohsugi & Kohjiro Ueki & Shinichi Oka & Masashi Mizokami & Takao Itoi & Takashi Kawai , 2022. "Extensive gut virome variation and its associations with host and environmental factors in a population-level cohort," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    6. María Dolores Ramos-Barbero & Clara Gómez-Gómez & Laura Sala-Comorera & Lorena Rodríguez-Rubio & Sara Morales-Cortes & Elena Mendoza-Barberá & Gloria Vique & Daniel Toribio-Avedillo & Anicet R. Blanch, 2023. "Characterization of crAss-like phage isolates highlights Crassvirales genetic heterogeneity and worldwide distribution," Nature Communications, Nature, vol. 14(1), pages 1-14, December.

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