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在小鼠模型中表达用于黏膜免疫的沙门氏菌鞭毛蛋白基因的基因工程动物双歧杆菌。

Genetically engineered Bifidobacterium animalis expressing the Salmonella flagellin gene for the mucosal immunization in a mouse model.

作者信息

Takata Tetsuo, Shirakawa Toshiro, Kawasaki Yoshiko, Kinoshita Shohiro, Gotoh Akinobu, Kano Yasunobu, Kawabata Masato

机构信息

International Center for Medical Research and Treatment, Kobe University School of Medicine, Kobe 650-0017, Japan.

出版信息

J Gene Med. 2006 Nov;8(11):1341-6. doi: 10.1002/jgm.963.

Abstract

BACKGROUND

A critical component of the host defense against enteric infections is the immunological response of the mucosal membrane, a major starting point of infectious disease, such as typhoid fever. The mucosal immune system consists of an integrated network of lymphoid tissues, mucous membrane-associated cells, and effector molecules. In the present study, we developed a recombinant Bifidobacterium animalis (B. animalis) genetically modified with the Salmonella flagellin gene for mucosal immunization as an oral typhoid vaccine.

METHODS

We constructed an oral vaccine against Salmonella typhimurium, consisting of recombinant B. animalis containing the flagellin gene of Salmonella. The recombinant B. animalis was administered orally to mice every other day for 6 weeks. Anti-flagellin antibodies in the serum and stools were measured by enzyme-linked immunosorbent assay (ELISA).

RESULTS

We detected significantly higher levels of flagellin-specific IgA in the serum and stools of the mice treated with the recombinant B. animalis containing the flagellin gene than was seen in those treated with parental B. animalis.

CONCLUSIONS

Our findings suggest that an oral vaccination using recombinant B. animalis genetically modified with the flagellin gene of Salmonella may be effective against Salmonella infections.

摘要

背景

宿主抵御肠道感染的关键组成部分是黏膜的免疫反应,黏膜是诸如伤寒热等传染病的主要起始点。黏膜免疫系统由淋巴组织、黏膜相关细胞和效应分子组成的综合网络构成。在本研究中,我们构建了一种经沙门氏菌鞭毛蛋白基因修饰的重组动物双歧杆菌(B. animalis),用于黏膜免疫,作为口服伤寒疫苗。

方法

我们构建了一种针对鼠伤寒沙门氏菌的口服疫苗,其由含有沙门氏菌鞭毛蛋白基因的重组动物双歧杆菌组成。重组动物双歧杆菌每隔一天口服给予小鼠,持续6周。通过酶联免疫吸附测定(ELISA)检测血清和粪便中的抗鞭毛蛋白抗体。

结果

我们检测到,与用亲本动物双歧杆菌处理的小鼠相比,用含有鞭毛蛋白基因的重组动物双歧杆菌处理的小鼠血清和粪便中鞭毛蛋白特异性IgA水平显著更高。

结论

我们的研究结果表明,使用经沙门氏菌鞭毛蛋白基因修饰的重组动物双歧杆菌进行口服疫苗接种可能对沙门氏菌感染有效。

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