Exploration of New Sites in Adenovirus Hexon for Foreign Peptides Insertion.

The Open Virology Journal Pub Date : 2015-05-29 eCollection Date: 2015-01-01 DOI:10.2174/1874357901509010001
Satyender Hansra, Sujit Pujhari, Alexander N Zakhartchouk
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引用次数: 4

Abstract

Adenoviral vectors are now being explored as vaccine carriers to prevent infectious diseases in humans and animals. There are two strategies aimed at the expression of a vaccine antigen by adenoviral vectors. The first includes an insertion of the foreign gene expression cassette into the E1 region. The second strategy is antigen incorporation into the viral capsid proteins. To extend this methodology, we have searched for new sites at the human adenovirus serotype 5 major capsid protein hexon for a vaccine antigen insertion. To this end, we utilized sites in the hexon hypervariable region (HVR) 7, 8 and 9 to display a 15-mer peptide containing the main neutralizing epitope of porcine reproductive and respiratory syndrome virus. However, we could not rescue the viruses with the insertions of the peptide into HVR 8 and 9, consistent with the viruses being unable to tolerate insertions at these sites. In contrast, the virus with the insertion of the peptide in HVR 7 was viable - growing well in cell culture and the inserted peptide was exposed on the virion surface.

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腺病毒六邻体外源肽插入新位点的探索。
目前正在探索腺病毒载体作为预防人类和动物传染病的疫苗载体。有两种策略旨在通过腺病毒载体表达疫苗抗原。第一种方法包括将外源基因表达盒插入E1区。第二种策略是将抗原整合到病毒衣壳蛋白中。为了扩展这一方法,我们在人腺病毒血清型5主要衣壳蛋白六邻体上寻找新的位点,用于疫苗抗原插入。为此,我们利用六邻体高变区(HVR) 7、8和9的位点,展示了一个包含猪繁殖与呼吸综合征病毒主要中和表位的15-mer肽。然而,我们无法通过将肽插入hvr8和9来挽救病毒,这与病毒无法耐受这些位点的插入一致。与此相反,在hvr7中插入肽的病毒在细胞培养中生长良好,并且插入的肽暴露在病毒粒子表面。
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