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The Helicobacter pylori Genome Project: insights into H. pylori population structure from analysis of a worldwide collection of complete genomes

Author

Listed:
  • Kaisa Thorell

    (University of Gothenburg)

  • Zilia Y. Muñoz-Ramírez

    (Universidad Autónoma de Chihuahua, Chihuahua)

  • Difei Wang

    (Frederick National Laboratory for Cancer Research
    National Cancer Institute)

  • Santiago Sandoval-Motta

    (Instituto Nacional de Medicina Genómica
    Consejo Nacional de Ciencia y Tecnologia, Cátedras CONACYT
    Universidad Nacional Autónoma de México)

  • Rajiv Boscolo Agostini

    (University of Ferrara)

  • Silvia Ghirotto

    (University of Ferrara)

  • Roberto C. Torres

    (Institute Pasteur Shanghai)

  • Daniel Falush

    (Institute Pasteur Shanghai)

  • M. Constanza Camargo

    (National Cancer Institute)

  • Charles S. Rabkin

    (National Cancer Institute)

Abstract

Helicobacter pylori, a dominant member of the gastric microbiota, shares co-evolutionary history with humans. This has led to the development of genetically distinct H. pylori subpopulations associated with the geographic origin of the host and with differential gastric disease risk. Here, we provide insights into H. pylori population structure as a part of the Helicobacter pylori Genome Project (HpGP), a multi-disciplinary initiative aimed at elucidating H. pylori pathogenesis and identifying new therapeutic targets. We collected 1011 well-characterized clinical strains from 50 countries and generated high-quality genome sequences. We analysed core genome diversity and population structure of the HpGP dataset and 255 worldwide reference genomes to outline the ancestral contribution to Eurasian, African, and American populations. We found evidence of substantial contribution of population hpNorthAsia and subpopulation hspUral in Northern European H. pylori. The genomes of H. pylori isolated from northern and southern Indigenous Americans differed in that bacteria isolated in northern Indigenous communities were more similar to North Asian H. pylori while the southern had higher relatedness to hpEastAsia. Notably, we also found a highly clonal yet geographically dispersed North American subpopulation, which is negative for the cag pathogenicity island, and present in 7% of sequenced US genomes. We expect the HpGP dataset and the corresponding strains to become a major asset for H. pylori genomics.

Suggested Citation

  • Kaisa Thorell & Zilia Y. Muñoz-Ramírez & Difei Wang & Santiago Sandoval-Motta & Rajiv Boscolo Agostini & Silvia Ghirotto & Roberto C. Torres & Daniel Falush & M. Constanza Camargo & Charles S. Rabkin, 2023. "The Helicobacter pylori Genome Project: insights into H. pylori population structure from analysis of a worldwide collection of complete genomes," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43562-y
    DOI: 10.1038/s41467-023-43562-y
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    References listed on IDEAS

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    1. Bodo Linz & François Balloux & Yoshan Moodley & Andrea Manica & Hua Liu & Philippe Roumagnac & Daniel Falush & Christiana Stamer & Franck Prugnolle & Schalk W. van der Merwe & Yoshio Yamaoka & David Y, 2007. "An African origin for the intimate association between humans and Helicobacter pylori," Nature, Nature, vol. 445(7130), pages 915-918, February.
    2. Harry A. Thorpe & Elise Tourrette & Koji Yahara & Filipa F. Vale & Siqi Liu & Mónica Oleastro & Teresa Alarcon & Tsachi-Tsadok Perets & Saeid Latifi-Navid & Yoshio Yamaoka & Beatriz Martinez-Gonzalez , 2022. "Repeated out-of-Africa expansions of Helicobacter pylori driven by replacement of deleterious mutations," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    3. Daniel John Lawson & Garrett Hellenthal & Simon Myers & Daniel Falush, 2012. "Inference of Population Structure using Dense Haplotype Data," PLOS Genetics, Public Library of Science, vol. 8(1), pages 1-16, January.
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