Phylogeny and disease associations of a widespread and ancient intestinal bacteriophage lineage

  • Patrick A. de Jonge
  • , Bert Jan H. van den Born
  • , Aeilko H. Zwinderman
  • , Max Nieuwdorp
  • , Bas E. Dutilh
  • , Hilde Herrema*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Viruses are core components of the human microbiome, impacting health through interactions with gut bacteria and the immune system. Most human microbiome viruses are bacteriophages, which exclusively infect bacteria. Until recently, most gut virome studies focused on low taxonomic resolution (e.g., viral operational taxonomic units), hampering population-level analyses. We previously identified an expansive and widespread bacteriophage lineage in inhabitants of Amsterdam, the Netherlands. Here, we study their biodiversity and evolution in various human populations. Based on a phylogeny using sequences from six viral genome databases, we propose the Candidatus order Heliusvirales. We identify heliusviruses in 82% of 5441 individuals across 39 studies, and in nine metagenomes from humans that lived in Europe and North America between 1000 and 5000 years ago. We show that a large lineage started to diversify when Homo sapiens first appeared some 300,000 years ago. Ancient peoples and modern hunter-gatherers have distinct Ca. Heliusvirales populations with lower richness than modern urbanized people. Urbanized people suffering from type 1 and type 2 diabetes, as well as inflammatory bowel disease, have higher Ca. Heliusvirales richness than healthy controls. We thus conclude that these ancient core members of the human gut virome have thrived with increasingly westernized lifestyles.

Original languageEnglish
Article number6346
JournalNature Communications
Volume15
Issue number1
DOIs
Publication statusPublished - 27 Jul 2024

Bibliographical note

Publisher Copyright:
© The Author(s) 2024.

Funding

P.A.d.J. was supported by a Talent Development grant of the Amsterdam Gastroenterology, Endocrinology, and Metabolism research school at the Amsterdam UMC and an Amsterdam University Fund Startstipendium. M.N. was supported by a personal ZONMW-VICI grant 2020 (09150182010020). B.E.D. was supported by the European Research Council (ERC) Consolidator grant 865694: DiversiPHI, the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany's Excellence Strategy-EXC 2051-Project-ID 390713860, the Alexander von Humboldt Foundation in the context of an Alexander von Humboldt-Professorship founded by German Federal Ministry of Education and Research, and the European Union's Horizon 2020 research and innovation program, under the Marie Sk & lstrok;odowska-Curie Actions Innovative Training Networks grant agreement no. 955974 (VIROINF). HH was supported by an Aspasia premium (015.017.050) and Dutch Diabetes Research Foundation (2019.82.004). The HELIUS study is conducted by the Amsterdam University Medical Centers, location AMC and the Public Health Service of Amsterdam. Both organizations provided core support for HELIUS. The HELIUS study is also funded by the Dutch Heart Foundation, the Netherlands Organization for Health Research and Development (ZonMw), the European Union (FP-7), and the European Fund for the Integration of non-EU immigrants (EIF). We are most grateful to the participants of the HELIUS study and the management team, research nurses, interviewers, research assistants and other staff who have taken part in gathering the data of this study.DAS:Datasets used in this work have all been previously published, and can be found in the following places: GPD; https://www.sanger.ac.uk/data/gut-phage-database/, GVD; https://doi.org/10.25739/12sq-k039, metagenomic gut virus catalog; https://portal.nersc.gov/MGV, IMG/VR; https://img.jgi.doe.gov/cgi-bin/vr/main.cgi, NCBI RefSeq; https://www.ncbi.nlm.nih.gov/refseq/. Contigs generated by Pasolli et al., 2019 can be found at http://segatalab.cibio.unitn.it/data/Pasolli_et_al.html, while sequencing reads can be found in the European Nucleotide Archive under accession numbers PRJNA561510, PRJEB44507, PRJNA278393, and PRJNA268964. Trees, assembled reads from ancient samples, genome annotations, protein clusters, and Ca. Heliusvirales genomes are available at Zenodo (https://doi.org/10.5281/zenodo.8328078). Source data are provided with this paper.

FundersFunder number
EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020)2020 (09150182010020)
Talent Development grant of the Amsterdam Gastroenterology, Endocrinology, and Metabolism research school at the Amsterdam UMC865694: DiversiPHI
European Research Council (ERC)390713860
Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)
Alexander von Humboldt Foundation955974, 015.017.050
European Union2019.82.004
Dutch Diabetes Research Foundation
Dutch Heart Foundation
Netherlands Organization for Health Research and Development (ZonMw)
European Union (FP-7)
European Fund for the Integration of non-EU immigrants (EIF)

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

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