Construction and expression of a recombinant plasmid containing the porcine epidemic diarrhea virus S1 gene delivered by Lactobacillus
Conference: BIBE 2019 - The Third International Conference on Biological Information and Biomedical Engineering
06/20/2019 - 06/22/2019 at Hangzhou, China
Proceedings: BIBE 2019
Pages: 5Language: englishTyp: PDFPersonal VDE Members are entitled to a 10% discount on this title
Deng, Yichao; Jiang, Ziyi; Fan, Yi; Mao, Xi-yu; Lv, Wen-ting; Zhu, Ling (Sichuan Provincial Key Laboratory of Animal Diseases and Human Health, Sichuan Agricultural University, Chengdu, Sichuan, China)
[Objective] To construct a recombinant lactobacillus capable of expressing the porcine epidemic diarrhea virus S1 gene, and to lay a foundation for subsequent research on oral vaccination against porcine epidemic diarrhea virus. [Methods] The bioinformatics software Protean was used to analyse the antigenicity of the PEDV S1 protein and the 307 amino acid neutralising epitope was screened and sent to Sangon Biotech Co., Ltd for codon optimisation. The plasmid was ligated to the pUC-57 clone plasmid to form the pUC57-S1 recombinant plasmid. The pVE5523 vector and the pUC57- S1 recombinant plasmid were enzymatically digested and the target gene was spliced into the final vector pVE5523 to obtain a recombinant plasmid pVE5523-S1, which was electroporated and transformed into Lactobacillus plantarum to obtain a recombinant Lactobacillus plantarum. The recombinant Lactobacillus plantarum was identified by western blot to demonstrate whether the target gene was expressed. [Result] The recombinant plasmids pUC57-S1 and pVE5523-S1 were successfully constructed using Lactobacillus plantarum as a template and the recombinant plasmids pUC57-S1 and pVE5523-S1 were successfully transformed. Western blot analysis showed that the recombinant Lactobacillus successfully expressed a recombinant protein with a relative molecular mass of approximately 34 kD.