Nature Communications (Sep 2024)

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

  • 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,
  • Martine Aubert,
  • Matthew P. Taylor,
  • Keith R. Jerome,
  • Eric Verdin

DOI
https://doi.org/10.1038/s41467-024-52395-2
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 18

Abstract

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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.