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首页> 外文期刊>Archives of virology >Development of novel antibodies against non-structural proteins nsP1, nsP3 and nsP4 of chikungunya virus: potential use in basic research
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Development of novel antibodies against non-structural proteins nsP1, nsP3 and nsP4 of chikungunya virus: potential use in basic research

机译:针对基孔肯雅病毒非结构蛋白nsP1,nsP3和nsP4的新型抗体的开发:在基础研究中的潜在用途

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摘要

Chikungunya virus (CHIKV) has reemerged recently as an important pathogen, causing several large epidemics worldwide. This necessitates the development of better reagents to understand its biology and to establish effective and safe control measures. The present study describes the development and characterization of polyclonal antibodies (pAbs) against synthetic peptides of CHIKV non-structural proteins (nsPs; nsP1, nsP3 and nsP4). The reactivity of these pAbs was demonstrated by ELISA and Western blot. Additionally, in vitro infection studies in a mammalian system confirmed that these pAbs are highly sensitive and specific for CHIKV nsPs, as these proteins were detected very early during viral replication. Homology analysis of the selected epitope sequences revealed that they are conserved among all of the CHIKV strains of different genotypes, while comparison with other alphavirus sequences showed that none of them are 100 % identical to the epitope sequences (except Onyong-nyong and Igbo Ora viruses, which show 100 % identity to the nsP4 epitope). Interestingly, two different forms of CHIKV nsP1 and three different forms of nsP3 were detected in Western blot analysis during infection; however, further experimental investigations are required to confirm their identity. Also, the use of these antibodies demonstrated faster and enhanced expression profiles of all CHIKV nsPs in 2006 Indian outbreak strains when compared to the CHIKV prototype strain, suggesting the epidemic potential of the 2006 isolate. Accordingly, it can be suggested that the pAbs reported in this study can be used as sensitive and specific tools for experimental investigations of CHIKV replication and infection.
机译:基孔肯雅病毒(CHIKV)最近作为一种重要的病原体重新出现,在世界范围内引起了数种大流行。这就需要开发更好的试剂来理解其生物学并建立有效而安全的控制措施。本研究描述了针对CHIKV非结构蛋白(nsPs; nsP1,nsP3和nsP4)合成肽的多克隆抗体(pAbs)的开发和表征。这些pAb的反应性通过ELISA和Western blot证实。此外,在哺乳动物系统中进行的体外感染研究证实,这些pAbs对CHIKV nsPs具有高度的敏感性和特异性,因为这些蛋白在病毒复制的早期就被检测到。对所选表位序列的同源性分析显示,它们在所有不同基因型的CHIKV菌株中都是保守的,而与其他alphavirus序列的比较表明,它们与表位序列均没有100%相同(Onyong-nyong和Igbo Ora病毒除外) ,与nsP4表位具有100%的同一性)。有趣的是,在感染过程中的蛋白质印迹分析中检测到两种不同形式的CHIKV nsP1和三种不同形式的nsP3。但是,需要进行进一步的实验研究以确认其身份。同样,与CHIKV原型毒株相比,使用这些抗体证明了2006年印度暴发病毒株中所有CHIKV nsPs的表达均得到了更快和增强的表达,表明2006年分离株的流行潜力。因此,可以建议本研究报道的pAb可以用作敏感和特定的工具用于CHIKV复制和感染的实验研究。

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