Genetically engineering of Saccharomyces cerevisiae for enhanced oral delivery vaccine vehicle

生物 酿酒酵母 重组DNA 基因敲除 dna疫苗 酵母 质粒 免疫系统 病毒学 微生物学 遗传学 基因
作者
Baoquan Han,Feng Yun Yue,Xiaojun Zhang,Kun Xu,Zhiying Zhang,Zhongyi Sun,Lu Mu,Xiaoyu Li
出处
期刊:Fish & Shellfish Immunology [Elsevier BV]
卷期号:146: 109425-109425
标识
DOI:10.1016/j.fsi.2024.109425
摘要

As a series of our previous studies reported, recombinant yeast can be the oral vaccines to deliver designed protein and DNA, as well as functional shRNA, into dendritic cells (DCs) in mice for specific immune regulation. Here, we report the further optimization of oral yeast-based vaccine from two aspects (yeast characteristics and recombinant DNA constitution) to improve the effect of immune regulation. After screening four genes in negative regulation of glucan synthesis in yeast (MNN9, GUP1, PBS2 and EXG1), this research combined HDR-based genome editing technology with Cre-loxP technology to acquire 15 gene-knockout strains without drug resistance-gene to exclude biosafety risks; afterward, oral feeding experiments were performed on the mice using 15 oral recombinant yeast-based vaccines constructed by the gene-knockout strains harboring pCMV-MSTN plasmid to screen the target strain with more effective inducing mstn-specific antibody which in turn increasing weight gain effect. And subsequently based on the selected gene-knockout strain, the recombinant DNA in the oral recombinant yeast-based vaccine is optimized via a combination of protein fusion expression (OVA-MSTN) and interfering RNA technology (shRNA-IL21), comparison in terms of both weight gain effect and antibody titer revealed that the selected gene-knockout strain (GUP1ΔEXG1Δ) combined with specific recombinant DNA (pCMV-OVA-MSTN-shIL2) had a better effect of the vaccine. This study provides a useful reference to the subsequent construction of a more efficient oral recombinant yeast-based vaccine in the food and pharmaceutical industry.
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