Acta Agriculturae Zhejiangensis ›› 2026, Vol. 38 ›› Issue (5): 867-875.DOI: 10.3969/j.issn.1004-1524.20250283

• Animal Science • Previous Articles     Next Articles

Expression of pseudorabies virus gD protein in rice cells and optimization of purification condition

KOU Shaokang1(), CHEN Hengyao1, PAN Shiyuan1, ZHANG Jiangnan1, CHENG Wenbo1, CHU Hongyan1, ZHANG Lei1, ZHANG Erqin1,2   

  1. 1 College of Veterinary Medicine, Henan Agricultural University, Zhengzhou 450046, China
    2 Key Laboratory of Animal Immunology, Henan Academy of Agricultural Sciences, Zhengzhou 450002, China
  • Received:2025-04-09 Online:2026-05-25 Published:2026-06-02

Abstract:

To explore the feasibility of expressing the pseudorabies virus gD protein in rice cells and to lay a foundation for developing a pseudorabies virus subunit vaccine, this study optimized and artificially synthesized the pseudorabies virus gD gene based on rice codon usage bias, constructing the recombinant plant expression vector pCAMBIA1300-gD. This vector was introduced into rice callus via Agrobacterium-mediated transformation, and resistant calluses were obtained after co-cultivation and dark culture screening. Callus genomic DNA was extracted using the CTAB method, and positive calluses were identified by PCR. Positive calluses were expanded in culture, ground, and added to liquid medium for shake-flask cultivation. Western blot was used to detect the expression of the gD protein. Based on the physicochemical properties of the target protein, purification conditions including pH value, cation exchange resin, and hydrophobic resin were screened and optimized. The results showed that 110 calluses were obtained after hygromycin screening, with 92 identified as positive by PCR, yielding a positive rate of 83.6%. Western blot analysis of 35 cell lines revealed successful gD protein expression in 15 lines. Purification via two-step chromatography using cation exchange resin 650F and hydrophobic resin GE Butyl 4FF yielded gD protein of certain purity. This study established a foundation for using rice as a bioreactor to produce pseudorabies virus subunit vaccines.

Key words: rice, callus, pseudorabies virus, plant expression vector, gD protein, codon optimization, protein purification

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