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含肠出血性大肠杆菌重组StxB抗原的壳聚糖纳米粒的制备及其在BALB/c小鼠中的免疫原性评价。

Preparation of chitosan nanoparticle containing recombinant StxB antigen of EHEC and evaluation its immunogenicity in BALB/c mice.

作者信息

Almasian Pegah, Amani Jafar, Arani Fahimeh Baghban, Nazarian Shahram, Kazemi Rouhollah, Tabrizi Niloufar Mirzaee

机构信息

Department of Genetics and Biotechnology, School of Biological Sciences, Varamin-Pishva Branch, Islamic Azad University, Varamin, Iran.

Applied Microbiology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Microbiol. 2018 Dec;10(6):361-370.

Abstract

BACKGROUND AND OBJECTIVES

O157:H7 is one of the most important food pathogens that produces colitis and bloody urine in humans. The Stx2B subunit is considered as one of the candidates for vaccine due to its immunogenic and adjuvant properties. Designing a mucosal vaccine using nanoparticles for protecting the antigen against degradation and controlling the release of antigen are important. The objective of the current study was to prepare nanoparticles containing the Stx2B subunit of O157:H7 and evaluation of its immunogenicity in the mouse model.

MATERIALS AND METHODS

BL21 DE3 and pET28a-stxB were used for expression of the gene. After inducing gene expression, purification of the Stx2b protein was performed. Then, chitosan nanoparticle containing recombinant Stx2B was prepared and administered to BALB/c mice. IgA and IgG titers in serum and IgA titers in feces of immunized and control mice were evaluated by the ELISA method.

RESULTS

After expression and purification of the Stx2B recombinant protein, an expected band of 13 kDa was observed on the SDS-PAGE gel and confirmed by Western Blot analysis. The size of the nanoparticle containing Stx2B was 290 nm. In the immunized mice, IgG and IgA titers were significantly increased. The immunized mice were challenged against O157:H7 Stx+ and the shedding analysis showed that colonization of bacteria in the intestinal tract decreased.

CONCLUSION

Oral administration of nanoparticles containing Stx2B as a candidate for the vaccine can induce a systemic and mucosal immune response against Stx2 toxin and can provide acceptable protection.

摘要

背景与目的

O157:H7是最重要的食源性病原体之一,可导致人类结肠炎和血尿。由于其免疫原性和佐剂特性,Stx2B亚基被认为是疫苗候选物之一。设计使用纳米颗粒的黏膜疫苗以保护抗原不被降解并控制抗原释放非常重要。本研究的目的是制备含有O157:H7的Stx2B亚基的纳米颗粒,并评估其在小鼠模型中的免疫原性。

材料与方法

使用BL21 DE3和pET28a-stxB进行基因表达。诱导基因表达后,对Stx2b蛋白进行纯化。然后,制备含有重组Stx2B的壳聚糖纳米颗粒并给予BALB/c小鼠。通过ELISA法评估免疫小鼠和对照小鼠血清中的IgA和IgG滴度以及粪便中的IgA滴度。

结果

Stx2B重组蛋白表达和纯化后,在SDS-PAGE凝胶上观察到预期的13 kDa条带,并通过Western Blot分析得到证实。含有Stx2B的纳米颗粒大小为290 nm。在免疫小鼠中,IgG和IgA滴度显著增加。对免疫小鼠进行O157:H7 Stx+攻击,脱落分析表明肠道中细菌的定植减少。

结论

口服含有Stx2B的纳米颗粒作为疫苗候选物可诱导针对Stx2毒素的全身和黏膜免疫反应,并可提供可接受的保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/896f/6414748/fed868837bb5/IJM-10-361-g001.jpg

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