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使用修饰的家蚕核型多角体病毒将犬新孢子虫抗原基因转导入哺乳动物细胞以生产抗体。

Transduction of a Neospora caninum antigen gene into mammalian cells using a modified Bombyx mori nucleopolyhedrovirus for antibody production.

作者信息

Kato Tatsuya, Itagaki Kohei, Yoshimoto Mai, Hiramatsu Rikito, Suhaimi Hamizah, Kohsaka Tetsuya, Park Enoch Y

机构信息

Laboratory of Biotechnology, Research Institute of Green Science and Technology, Shizuoka University, 836 Ohya Suruga-ku, Shizuoka 422-8529, Japan; Laboratory of Biotechnology, Division of Applied Biological Chemistry, College of Agriculture, Shizuoka University, 836 Ohya Suruga-ku, Shizuoka 422-8529, Japan; Laboratory of Biotechnology, Department of Bioscience, Graduate School of Science and Technology, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka 422-8529, Japan.

Laboratory of Biotechnology, Division of Applied Biological Chemistry, College of Agriculture, Shizuoka University, 836 Ohya Suruga-ku, Shizuoka 422-8529, Japan.

出版信息

J Biosci Bioeng. 2017 Dec;124(6):606-610. doi: 10.1016/j.jbiosc.2017.06.015. Epub 2017 Jul 14.

Abstract

Autographa californica multiple nucleopolyhedrovirus (AcMNPV) can easily enter and transduce foreign genes into mammalian cells, but these functions are difficult for Bombyx mori nucleopolyhedrovirus (BmNPV). In this study, we investigated the induction of antibody production in mice immunized with an engineered BmNPV. The GP64 of BmNPV (BmGP64) was replaced with the GP64 of AcMNPV (AcGP64); this construct, designated BmNPVΔbgp/AcGP64, displays AcGP64 on the surface of BmNPV. The Neospora caninum antigen (NcSRS2) expression cassette, consisting of the cytomegalovirus immediate-early promoter and NcSRS2 from N. caninum, was inserted into BmNPVΔbgp/AcGP64; this construct was designated BmNPVΔbgp/AcGP64/SRS2. For comparison, AcMNPV/SRS2, which contains the same NcSRS2 expression cassette as for BmNPVΔbgp/AcGP64, was also constructed. NcSRS2 was expressed in HEK293T cells when the engineered BmNPVs were transduced at a multiplicity of infection of 150. BmNPVΔbgp/AcGP64/SRS2 induced the production of NcSRS2-specific antibodies in mice, whereas AcMNPV/SRS2 and the control BmNPV did not. These results suggest that BmNPV prepared from silkworm hemolymph induces the production of antigen-specific antibodies in immunized mice and can be used for antibody production and vaccine development.

摘要

苜蓿银纹夜蛾多核衣壳核型多角体病毒(AcMNPV)能够轻易进入哺乳动物细胞并转导外源基因,但家蚕核型多角体病毒(BmNPV)却很难做到这些功能。在本研究中,我们调查了用工程化BmNPV免疫的小鼠体内抗体产生的诱导情况。将BmNPV的GP64(BmGP64)替换为AcMNPV的GP64(AcGP64);这种构建体,命名为BmNPVΔbgp/AcGP64,可在BmNPV表面展示AcGP64。将由巨细胞病毒立即早期启动子和来自犬新孢子虫的NcSRS2组成的犬新孢子虫抗原(NcSRS2)表达盒插入BmNPVΔbgp/AcGP64;这种构建体命名为BmNPVΔbgp/AcGP64/SRS2。为作比较,还构建了含有与BmNPVΔbgp/AcGP64相同的NcSRS2表达盒的AcMNPV/SRS2。当以感染复数150转导工程化BmNPV时,NcSRS2在HEK293T细胞中表达。BmNPVΔbgp/AcGP64/SRS2在小鼠中诱导产生NcSRS2特异性抗体,而AcMNPV/SRS2和对照BmNPV则不能。这些结果表明,从家蚕血淋巴制备的BmNPV可在免疫小鼠中诱导产生抗原特异性抗体,可用于抗体生产和疫苗开发。

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