Expression of Recombinant Non Structural 1 Protein of Dengue Virus Serotype-2 in Mammalian Cell Line

I. Rusmana
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引用次数: 2

Abstract

Dengue infection is a global infectious disease with almost 100 million cases occur annually in over more than 100 endemic countries. Dengue virus (DENV), the causative agent of dengue infection, is an 11 kbp RNApositive strand virus which encode 3 structural and 7 non-structural protein within its genome. Non-structural 1 (NS1) protein of DENV is expressed in the earlier stage of infection and having pathogenic role in disease severity. NS1 gene of DENV serotype-2 Indonesian strain was amplified through PCR method using specific designated primers. NS1 amplicon were then cloned into pUMVC4.a and pcDNA3.1 mammalian expression vector which confirmed through colony PCR and sequencing method. Recombinant pUNS1 and pcNS1 plasmids were transfected into CHO-K1 mammalian cell line with lipid based method. Recombinant NS1 protein expression were analyzed through immunostaining using dengue patient sera and rapid NS1 detection kit. Recombinant pUNS1 and pcNS1 plasmids were successfully constructed and recombinant NS1 protein was expressed in CHOK1 mammalian cell line and shown to be reactive against dengue patient sera. Our recombinant NS1 protein also tend to be released outside the transfected CHO-K1 cells as detected in rapid NS1 detection kit. Recombinant dengue NS1 protein was expressed in mammalian cell line in both intra and extracellularly and shown to be immunogenic.
重组2型登革病毒非结构1蛋白在哺乳动物细胞系中的表达
登革热感染是一种全球性传染病,每年在100多个流行国家发生近1亿例病例。登革热病毒(DENV)是一种11 kbp的rna阳性链病毒,在其基因组中编码3种结构蛋白和7种非结构蛋白。DENV的非结构1 (Non-structural 1, NS1)蛋白在感染早期表达,对疾病的严重程度有致病作用。采用特异引物PCR扩增DENV 2型印尼株NS1基因。然后将NS1扩增子克隆到pUMVC4中。a和pcDNA3.1的哺乳动物表达载体,通过集落PCR和测序方法确认。用脂质法将重组pUNS1和pcNS1质粒转染CHO-K1哺乳动物细胞系。采用登革热患者血清和NS1快速检测试剂盒进行免疫染色,分析重组NS1蛋白的表达。成功构建了重组pUNS1和pcNS1质粒,并在CHOK1哺乳动物细胞系中表达了重组NS1蛋白,显示出对登革热患者血清的反应性。我们的重组NS1蛋白也倾向于在转染CHO-K1细胞外释放,通过快速NS1检测试剂盒检测到。重组登革NS1蛋白在哺乳动物细胞系细胞内和细胞外均有表达,具有免疫原性。
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