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Development of canine herpesvirus based antifertility vaccines for foxes using bacterial artificial chromosomes

机译:使用细菌人工染色体开发基于犬疱疹病毒的狐狸抗生育力疫苗

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Using bacterial artificial chromosome (BAC) technology, a canine herpesvirus (CHV)-based recombinant vaccine vector was produced for the development of an antifertility vaccine for foxes. Infectious viruses were recovered following transfection of canid cells with a BAC plasmid carrying the complete CHV genome. In vitro growth characteristics of BAC-derived viruses were similar to that of wildtype (wt)-CHV. Two recombinant antigens, fox zona pellucida protein subunit 3 (fZPC) and enhanced green fluorescent protein (EGFP) as control antigen, were inserted into thymidine kinase (TK) locus of the CHV genome and shown to be efficiently expressed in vitro. Inoculation of foxes with transgenic CHVs induced CHV specific antibodies, but was innocuous and failed to elicit transgene-specific antibody responses. Infectious virus or viral DNA was not detected in mucosal secretions or tissues of vaccinated foxes. The CHV-BAC system proved to be a quick and reliable method to manipulate the CHV genome. It will help to readily apply changes in the vector design in order to improve virus replication in vivo.
机译:使用细菌人工染色体(BAC)技术,生产了基于犬疱疹病毒(CHV)的重组疫苗载体,用于开发狐狸抗生育力疫苗。用携带完整CHV基因组的BAC质粒转染犬科动物细胞后,回收了感染性病毒。 BAC衍生病毒的体外生长特性与野生型(wt)-CHV相似。将两个重组抗原,即狐带透明质蛋白亚基3(fZPC)和增强的绿色荧光蛋白(EGFP)作为对照抗原,插入到CHV基因组的胸苷激酶(TK)基因座中,并显示在体外有效表达。用转基因CHV接种狐狸可诱导出CHV特异性抗体,但无害且未能引起转基因特异性抗体反应。在狐狸的粘膜分泌物或组织中未检测到传染性病毒或病毒DNA。 CHV-BAC系统被证明是一种操作CHV基因组的快速而可靠的方法。这将有助于在载体设计中轻松应用更改,以改善体内病毒复制。

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