IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v11y2020i1d10.1038_s41467-020-14730-1.html
   My bibliography  Save this article

Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance

Author

Listed:
  • Bin Zhu

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health)

  • Yanzi Xiao

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health)

  • Meredith Yeager

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health
    Cancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research)

  • Gary Clifford

    (Infections and Cancer Epidemiology Group, International Agency for Research on Cancer)

  • Nicolas Wentzensen

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health)

  • Michael Cullen

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health
    Cancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research)

  • Joseph F. Boland

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health
    Cancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research)

  • Sara Bass

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health
    Cancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research)

  • Mia K. Steinberg

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health
    Cancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research)

  • Tina Raine-Bennett

    (Women’s Health Research Institute, Division of Research, Kaiser Permanente Northern California)

  • DongHyuk Lee

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health)

  • Robert D. Burk

    (Departments of Pediatrics, Microbiology and Immunology, and Obstetrics & Gynecology and Women’s Health, Albert Einstein College of Medicine
    Department of Epidemiology and Population Health, Albert Einstein College of Medicine)

  • Maisa Pinheiro

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health)

  • Lei Song

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health
    Cancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research)

  • Michael Dean

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health)

  • Chase W. Nelson

    (Sackler Institute for Comparative Genomics, American Museum of Natural History)

  • Laurie Burdett

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health
    Cancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research)

  • Kai Yu

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health)

  • David Roberson

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health
    Cancer Genomics Research Laboratory, Frederick National Laboratory for Cancer Research)

  • Thomas Lorey

    (Regional Laboratory, Kaiser Permanente Northern California)

  • Silvia Franceschi

    (CRO Aviano National Cancer Institute IRCCS)

  • Philip E. Castle

    (Department of Epidemiology and Population Health, Albert Einstein College of Medicine)

  • Joan Walker

    (University of Oklahoma Health Sciences Center)

  • Rosemary Zuna

    (University of Oklahoma Health Sciences Center)

  • Mark Schiffman

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health)

  • Lisa Mirabello

    (Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health)

Abstract

HPV16 causes half of cervical cancers worldwide; for unknown reasons, most infections resolve within two years. Here, we analyze the viral genomes of 5,328 HPV16-positive case-control samples to investigate mutational signatures and the role of human APOBEC3-induced mutations in viral clearance and cervical carcinogenesis. We identify four de novo mutational signatures, one of which matches the COSMIC APOBEC-associated signature 2. The viral genomes of the precancer/cancer cases are less likely to contain within-host somatic HPV16 APOBEC3-induced mutations (Fisher’s exact test, P = 6.2 x 10−14), and have a 30% lower nonsynonymous APOBEC3 mutation burden compared to controls. We replicate the low prevalence of HPV16 APOBEC3-induced mutations in 1,749 additional cases. APOBEC3 mutations also historically contribute to the evolution of HPV16 lineages. We demonstrate that cervical infections with a greater burden of somatic HPV16 APOBEC3-induced mutations are more likely to be benign or subsequently clear, suggesting they may reduce persistence, and thus progression, within the host.

Suggested Citation

  • Bin Zhu & Yanzi Xiao & Meredith Yeager & Gary Clifford & Nicolas Wentzensen & Michael Cullen & Joseph F. Boland & Sara Bass & Mia K. Steinberg & Tina Raine-Bennett & DongHyuk Lee & Robert D. Burk & Ma, 2020. "Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance," Nature Communications, Nature, vol. 11(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-14730-1
    DOI: 10.1038/s41467-020-14730-1
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-020-14730-1
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-020-14730-1?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Maisa Pinheiro & Nicolas Wentzensen & Michael Dean & Meredith Yeager & Zigui Chen & Amulya Shastry & Joseph F. Boland & Sara Bass & Laurie Burdett & Thomas Lorey & Sambit Mishra & Philip E. Castle & M, 2024. "Somatic mutations in 3929 HPV positive cervical cells associated with infection outcome and HPV type," Nature Communications, Nature, vol. 15(1), pages 1-12, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-14730-1. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.