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Background <p>The continuous evolution and cross-species transmission risk of pseudorabies virus (PRV) poses a substantial threat to the swine industry and public health. Nectin-1, an essential host receptor for PRV entry, represents a promising antiviral target; however, direct gene knockout (KO) raises biosafety concerns, and conventional genome-editing approaches remain inefficient for precise multiplex modification of critical functional residues.</p> Results <p>Here, we employed prime editing (PE) to systematically re-engineer the PRV entry receptor Nectin-1, introducing single and combinatorial point mutations at four structurally defined amino acids within the gD-binding interface. PE enable efficient homozygous multiplex editing of these functionally critical residues in porcine cells. Functional analyses showed that these targeted mutations specifically impaired viral internalization without affecting attachment and exhibited combinatorial effects, resulting in reductions in viral replication and release. Notably, the quadruple-site mutant conferred a level of resistance comparable to that observed in Nectin-1 KO cells.</p> Conclusion <p>Collectively, this study establishes a framework for “functional knockout,” in which precise editing of essential microdomains confers resistance to virus infection while preserving protein integrity. These findings, derived from in vitro cellular models, suggest a potentially safer and more controllable strategy for antiviral genome-edited breeding, pending further validation in vivo.</p>

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Prime editing of Nectin-1 functional domains confers knockout-level resistance to pseudorabies virus

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2026年5月29日

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  • Tangyuan Xie,
  • Hanxi Ouyang,
  • Yan Wang,
  • Shuhui Zhang,
  • Shuaikang Yang,
  • Jing Kong,
  • Tian Huang,
  • Gengsheng Cao

摘要

Background

The continuous evolution and cross-species transmission risk of pseudorabies virus (PRV) poses a substantial threat to the swine industry and public health. Nectin-1, an essential host receptor for PRV entry, represents a promising antiviral target; however, direct gene knockout (KO) raises biosafety concerns, and conventional genome-editing approaches remain inefficient for precise multiplex modification of critical functional residues.

Results

Here, we employed prime editing (PE) to systematically re-engineer the PRV entry receptor Nectin-1, introducing single and combinatorial point mutations at four structurally defined amino acids within the gD-binding interface. PE enable efficient homozygous multiplex editing of these functionally critical residues in porcine cells. Functional analyses showed that these targeted mutations specifically impaired viral internalization without affecting attachment and exhibited combinatorial effects, resulting in reductions in viral replication and release. Notably, the quadruple-site mutant conferred a level of resistance comparable to that observed in Nectin-1 KO cells.

Conclusion

Collectively, this study establishes a framework for “functional knockout,” in which precise editing of essential microdomains confers resistance to virus infection while preserving protein integrity. These findings, derived from in vitro cellular models, suggest a potentially safer and more controllable strategy for antiviral genome-edited breeding, pending further validation in vivo.