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基于血凝素神经氨酸酶蛋白的新城疫病毒多表位疫苗预测与分析

Prediction and analysis of multi epitope based vaccine against Newcastle disease virus based on haemagglutinin neuraminidase protein.

作者信息

Raza Adnan, Asif Rasheed Muhammad, Raza Sohail, Tariq Navid Muhammad, Afzal Amna, Jamil Farrukh

机构信息

Department of Biosciences, COMSATS University Islamabad, Sahiwal Campus, Sahiwal, Pakistan.

Institute of Microbiology, University of Veterinary and Animal Sciences, Lahore, Pakistan.

出版信息

Saudi J Biol Sci. 2022 Apr;29(4):3006-3014. doi: 10.1016/j.sjbs.2022.01.036. Epub 2022 Jan 20.

Abstract

Newcastle disease virus (NDV), an avian orthoavulavirus, is a causative agent of Newcastle disease named (NDV), and can cause even the epidemics when disease is not treated. Previously several vaccines based on attenuated and inactivated viruses have been reported which are rendered useless with the passage of time due to versatile changes in viral genome. Therefore, we aimed to develop an effective multi-epitope vaccine against the haemagglutinin neuraminidase (HN) protein of 26 NDV strains from Pakistan through a modern immunoinformatic approaches. As a result, a vaccine chimaera was constructed by combining T-cell and B-cell epitopes with the appropriate linkers and adjuvant. The designed vaccine was highly immunogenic, non-allergen and antigenic; therefore, the potential 3D-structureof multi epitope vaccine was constructed, refined and validated. A molecular docking study of a multiepitope vaccine candidate with the chicken Toll-like receptor-4 indicated successful binding. An immunological simulation was used to evaluate the candidate vaccine's ability to elicit an effective immune response. According to the computational studies, the proposed multiepitope vaccine is physically stable and may induce immune responses whichsuggested it a strong candidate against 26 Newcastle disease virus strains from Pakistan.

摘要

新城疫病毒(NDV)是一种禽正黏病毒,是新城疫(ND)的病原体,若不治疗,可引发疫情。此前已有多种基于减毒和灭活病毒的疫苗报道,但由于病毒基因组的多种变化,这些疫苗随着时间的推移变得无用。因此,我们旨在通过现代免疫信息学方法,开发一种针对来自巴基斯坦的26种新城疫病毒株血凝素神经氨酸酶(HN)蛋白的有效多表位疫苗。结果,通过将T细胞和B细胞表位与合适的连接子和佐剂相结合,构建了一种疫苗嵌合体。设计的疫苗具有高度免疫原性、无过敏原且具有抗原性;因此,构建、优化并验证了多表位疫苗的潜在三维结构。对一种多表位疫苗候选物与鸡Toll样受体-4进行的分子对接研究表明结合成功。使用免疫模拟来评估候选疫苗引发有效免疫反应的能力。根据计算研究,所提出的多表位疫苗在物理上是稳定的,可能诱导免疫反应,这表明它是对抗来自巴基斯坦的26种新城疫病毒株的有力候选疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d897/9073007/ee65c83e8468/gr1.jpg

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