A comprehensive functional landscape of PRV replication and pathogenesis revealed by genome-wide transposon
Wanwan Yan1, Keyue Ruan1, Lingchao Chen1
1Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai 200241, China.
Abstract:
Pseudorabies virus (PRV) is a large double-stranded DNA alphaherpesvirus with a genome of approximately 145 kb containing nearly 70 genes. To systematically profile gene functions, we constructed a genome-wide mutant library by performing Tn5 transposon mutagenesis on the PRV infectious clone pBAC-JS2012. Through transposon sequencing, 277 BAC plasmids (pBAC-JS2012) containing a single-copy transposon insertion in the PRV genome were screened from 352 clones, achieving mutations in 52 viral genes. Functional characterization demonstrated that 20 genes were essential for viral replication, while 8 genes, though non-essential, significantly modulated replication efficiency in vitro. Mutations in other 22 genes showed no significant effect on viral replication. In a mouse infection model, eight genes were identified as critical determinants of viral pathogenicity. Collectively, this genome-wide analysis delineates the functional landscape of PRV, classifying genes essential for replication and those contributing to virulence. This study not only advances the understanding of PRV genome organization and function, but also provides a rational basis for developing targeted antiviral interventions and attenuated vaccines.
Insights
Researchers mapped functions for nearly all genes in Pseudorabies virus (PRV), identifying essential genes for replication and virulence factors. This provides a foundation for developing new PRV antiviral therapies and vaccines.
Area of Science:
- Virology
- Genomics
- Molecular Biology
Background:
- Pseudorabies virus (PRV) is a significant alphaherpesvirus.
- Understanding PRV gene function is crucial for disease control.
Purpose of the Study:
- To systematically profile the function of PRV genes.
- To identify genes essential for viral replication and pathogenicity.
Main Methods:
- Genome-wide mutant library construction using Tn5 transposon mutagenesis.
- Transposon sequencing to identify single-copy insertion mutants.
- Functional characterization of mutated genes in vitro and in a mouse model.
Main Results:
- Mutations were generated in 52 PRV genes.
- 20 genes were found essential for viral replication.
- 8 genes significantly modulated replication, and 8 genes were critical for pathogenicity.
Conclusions:
- This study provides a comprehensive functional landscape of the PRV genome.
- Identified essential genes and virulence determinants offer targets for antiviral interventions.
- Findings support the development of novel PRV vaccines.
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