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枯草芽孢杆菌重组和非重组孢子展示技术的组合,用于在单个孢子上展示抗原和佐剂。

The combination of recombinant and non-recombinant Bacillus subtilis spore display technology for presentation of antigen and adjuvant on single spore.

机构信息

Department of Medical Biotechnology, Intercollegiate Faculty of Biotechnology UG-MUG, University of Gdańsk, Gdańsk, Poland.

Department of Microbiology, Faculty of Biology, University of Gdańsk, Gdańsk, Poland.

出版信息

Microb Cell Fact. 2017 Sep 12;16(1):151. doi: 10.1186/s12934-017-0765-y.

Abstract

BACKGROUND

Bacillus subtilis spores can be used for presentation of heterologous proteins. Two main approaches have been developed, the recombinant one, requiring modification of bacterial genome to express a protein of interest as a fusion with spore-coat protein, and non-recombinant, based on the adsorption of a heterologous protein onto the spore. So far only single proteins have been displayed on the spore surface.

RESULTS

We have used a combined approach to adsorb and display FliD protein of Clostridium difficile on the surface of recombinant IL-2-presenting spores. Such spores presented FliD protein with efficiency comparable to FliD-adsorbed spores produced by wild-type 168 strain and elicited FliD-specific immune response in intranasally immunized mice.

CONCLUSIONS

Our results indicate that such dual display technology may be useful in creation of spores simultaneously presenting adjuvant and antigen molecules. Regarding the characteristics of elicited immune response it seems plausible that such recombinant IL-2-presenting spores with adsorbed FliD protein might be an interesting candidate for vaccine against infections with Clostridium difficile.

摘要

背景

枯草芽孢杆菌孢子可用于异源蛋白的呈现。目前已经开发出两种主要方法,一种是重组方法,需要修饰细菌基因组以表达融合有孢子衣蛋白的目的蛋白;另一种是非重组方法,基于异源蛋白吸附到孢子上。到目前为止,只有单一蛋白被展示在孢子表面上。

结果

我们使用联合方法将艰难梭菌的 FliD 蛋白吸附并展示在重组 IL-2 呈现孢子的表面上。这些孢子呈现的 FliD 蛋白的效率可与野生型 168 株产生的吸附 FliD 蛋白的孢子相媲美,并在鼻腔内免疫的小鼠中引发了针对 FliD 的免疫反应。

结论

我们的结果表明,这种双重展示技术可能有助于同时呈现佐剂和抗原分子的孢子的创建。就所引发的免疫反应的特征而言,具有吸附 FliD 蛋白的这种重组 IL-2 呈现孢子可能是针对艰难梭菌感染的疫苗的一个有趣候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/842e/5596941/8ea4edfe01d2/12934_2017_765_Fig1_HTML.jpg

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