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Updated: Apr 10, 2026

Generating Recombinant Avian Herpesvirus Vectors with CRISPR/Cas9 Gene Editing
Published on: January 7, 2019
Research note: A novel double-gene deleted vaccine against hypervirulent MDV variant generated by CRISPR/Cas9-based
Lu Han1, Shu-Ge Wang2, Man Teng2
1College of Animal Science and Technology & Laboratory of Functional Microbiology and Animal Health, Henan University of Science and Technology, Luoyang 471003, PR China; Institute for Animal Health & UK-China Center of Excellence for Research on Avian Disease, Henan Academy of Agricultural Sciences, Zhengzhou 450002, PR China.
Abstract:
Marek's disease (MD), an important avian immunosuppressive and neoplastic diseases, has resulted in huge economic losses for the poultry industry worldwide. Over the past 50 years, the long-term prevalence of this disease and the growing immune pressure of MD vaccination have triggered persistently increased virulence. The emerging hypervirulent variant of MDV (HV-MDV) overcomes the protection conferred by commercial vaccines, highlighting the urgent need to develop novel, highly efficient MD vaccines. To address this challenge, using CRISPR/Cas9-based gene editing, we generated a novel candidate vaccine, SQ01ΔmeqΔLAT, which features double deletions of both oncogene meq and LAT-clustered miRNAs. Comprehensive experiments confirmed the gene deletions, genetic stability and retention of the replication kinetics of the mutant, without revealing any adverse impact on the expression of essential viral genes. Further animal experiments showed no histopathological lesions or neoplastic changes in SQ01ΔmeqΔLAT-challenged birds, demonstrating favourable safety to chicken hosts. More importantly, the SQ01ΔmeqΔLAT vaccine achieved a high protection index (PI) of 88.9% against HV-MDV strain HNSQ01; this was an improvement compared to CVI988, which provided a PI value of only 70.6%. Our data provide an important basis for the development of highly efficient MD vaccines and shed new light on the design of herpesvirus vaccines, simultaneously targeting both viral protein-coding genes and non-coding RNAs.
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