Expression of Hemagglutinin-Neuraminidase (HN) and Fusion (F) Epitopes of Newcastle Disease Virus (NDV) in Chlamydomonas reinhardtii

A. Shahriari, A. Afsharifar, M. Habibi-Pirkoohi
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引用次数: 3

Abstract

Owing to their unique characteristics which combines the properties of both prokaryotes and eukaryotes, microalgae have emerged as an ideal platform for heterologous production of recombinant proteins including subunit vaccines. In an attempt to develop recombinant vaccine against Newcastle Disease, an agrobacterium-mediated genetic transformation was carried out to express a chimeric gene construct including Hemagglutinin-Neuraminidase (HN) and Fusion (F) epitopes of Newcastle Disease Virus (NDV) in Chlamydomonas reinhardtii. Four tandem repeat of HN epitope with 96bp length followed by three tandem repeat of F epitope of NDV with 153bp length were used. Microalgal cells (Chlamydomonas reinhardtii) were co-cultivated with Agrobacterium tumefaciens cells harboring foreign gene construct and then transferred to selection medium. Single colonies representing putative transformation events were screened in selection medium enriched with kanamycin. PCR assay confirmed integration of F-HN sequence in microalgal nuclei. RT-PCR assay showed that the F-HN sequence was expressed in transformed colonies. Finally, translation of the foreign gene was confirmed by protein dot blotting, western blot and Elisa assay. The results of this experiment may contain both research and practical implications.
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新城疫病毒(NDV)血凝素-神经氨酸酶(HN)和融合(F)表位在莱茵衣单胞菌中的表达
由于其结合了原核生物和真核生物特性的独特特性,微藻已成为异源生产包括亚单位疫苗在内的重组蛋白的理想平台。为了研制新城疫重组疫苗,采用农杆菌介导的基因转化方法,在莱茵衣单胞菌中表达了新城疫病毒(NDV)血凝素-神经氨酸酶(HN)和融合(F)表位的嵌合基因构建体。HN表位的4个串联重复长度为96bp, NDV表位的3个串联重复长度为153bp。将莱茵衣藻(Chlamydomonas reinhardtii)微藻细胞与含有外源基因构建的农杆菌(Agrobacterium tumefaciens)细胞共培养,然后转移到选择培养基上。在富含卡那霉素的选择培养基中筛选代表假定转化事件的单个菌落。PCR检测证实F-HN序列整合在微藻细胞核中。RT-PCR结果显示,F-HN序列在转化菌落中表达。最后通过蛋白点印迹、蛋白印迹和酶联免疫吸附试验证实外源基因的翻译。这个实验的结果可能既有研究意义又有实际意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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