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Viral gene drive spread during herpes simplex virus 1 infection in mice

Author

Listed:
  • Marius Walter

    (Fred Hutch Cancer Center
    Buck Institute for Research on Aging)

  • Anoria K. Haick

    (Fred Hutch Cancer Center)

  • Rebeccah Riley

    (Buck Institute for Research on Aging)

  • Paola A. Massa

    (Fred Hutch Cancer Center)

  • Daniel E. Strongin

    (University of Washington)

  • Lindsay M. Klouser

    (Fred Hutch Cancer Center)

  • Michelle A. Loprieno

    (Fred Hutch Cancer Center)

  • Laurence Stensland

    (University of Washington)

  • Tracy K. Santo

    (University of Washington)

  • Pavitra Roychoudhury

    (Fred Hutch Cancer Center
    University of Washington)

  • Martine Aubert

    (Fred Hutch Cancer Center)

  • Matthew P. Taylor

    (Montana State University)

  • Keith R. Jerome

    (Fred Hutch Cancer Center
    University of Washington)

  • Eric Verdin

    (Buck Institute for Research on Aging)

Abstract

Gene drives are genetic modifications designed to propagate efficiently through a population. Most applications rely on homologous recombination during sexual reproduction in diploid organisms such as insects, but we recently developed a gene drive in herpesviruses that relies on co-infection of cells by wild-type and engineered viruses. Here, we report on a viral gene drive against human herpes simplex virus 1 (HSV-1) and show that it propagates efficiently in cell culture and during HSV-1 infection in mice. We describe high levels of co-infection and gene drive-mediated recombination in neuronal tissues during herpes encephalitis as the infection progresses from the site of inoculation to the peripheral and central nervous systems. In addition, we show evidence that a superinfecting gene drive virus could recombine with wild-type viruses during latent infection. These findings indicate that HSV-1 achieves high rates of co-infection and recombination during viral infection, a phenomenon that is currently underappreciated. Overall, this study shows that a viral gene drive could spread in vivo during HSV-1 infection, paving the way toward therapeutic applications.

Suggested Citation

  • Marius Walter & Anoria K. Haick & Rebeccah Riley & Paola A. Massa & Daniel E. Strongin & Lindsay M. Klouser & Michelle A. Loprieno & Laurence Stensland & Tracy K. Santo & Pavitra Roychoudhury & Martin, 2024. "Viral gene drive spread during herpes simplex virus 1 infection in mice," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-52395-2
    DOI: 10.1038/s41467-024-52395-2
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    References listed on IDEAS

    as
    1. Martine Aubert & Anoria K. Haick & Daniel E. Strongin & Lindsay M. Klouser & Michelle A. Loprieno & Laurence Stensland & Tracy K. Santo & Meei-Li Huang & Ollivier Hyrien & Daniel Stone & Keith R. Jero, 2024. "Gene editing for latent herpes simplex virus infection reduces viral load and shedding in vivo," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    2. Martine Aubert & Daniel E. Strongin & Pavitra Roychoudhury & Michelle A. Loprieno & Anoria K. Haick & Lindsay M. Klouser & Laurence Stensland & Meei-Li Huang & Negar Makhsous & Alexander Tait & Harsha, 2020. "Gene editing and elimination of latent herpes simplex virus in vivo," Nature Communications, Nature, vol. 11(1), pages 1-15, December.
    3. Marius Walter & Eric Verdin, 2020. "Viral gene drive in herpesviruses," Nature Communications, Nature, vol. 11(1), pages 1-11, December.
    Full references (including those not matched with items on IDEAS)

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