首页> 外文期刊>American Journal of Infectious Diseases and Microbiology >Immunoinformatics Predication and in silico Modeling of Epitope-Based Peptide Vaccine Against virulent Newcastle Disease Viruses
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Immunoinformatics Predication and in silico Modeling of Epitope-Based Peptide Vaccine Against virulent Newcastle Disease Viruses

机译:基于抗原表位的强毒新城疫病毒肽疫苗的免疫信息学预测和计算机模拟

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ewcastle disease virus (NDV) is negative sense single stranded RNA belongs to the Avulavirus genus of the Paramyxoviridae family which can be transmitted by inhalation or ingestion. Birds infected shed these viruses in feces as well as respiratory secretions. The aim of this study is to analyze fusion (F) protein of all virulent Newcastle strains reported in NCBI database using insilico approaches to select all possible epitopes that can be used as a therapeutic peptide vaccine. A total of 56 virulent NDV fusion protein variants retrieved from NCBI database. the conserved regions were introduced into IEDB analysis resource to predict B and T cell epitopes, as well as predicting the binding affinity of the conserved epitopes with BF2 21:01, from the predominantly expressed chicken MHC I molecule. Epitopes with high scores in both B and T cell epitopes predicting tools were suggested. Peptide vaccine against virulent NDV is strongly supersedes the conventional vaccines, as it designed to cover variant virulent mutated strains, which will reduce the recurrent outbreaks and their huge accompanied economical loss to a minimum.
机译:ewcastle病病毒(NDV)是阴性的单链RNA,属于副粘病毒科的Avulavirus属,可以通过吸入或摄入传播。被感染的鸟类通过粪便以及呼吸道分泌物中释放出了这些病毒。这项研究的目的是使用insilico方法分析在NCBI数据库中报告的所有有毒新城疫毒株的融合蛋白(F),以选择可用作治疗性肽疫苗的所有可能的表位。从NCBI数据库中检索到总共56种有毒NDV融合蛋白变异体。将保守区域引入IEDB分析资源,以预测B和T细胞表位,并预测主要表达的鸡MHC I分子与BF2 21:01的保守表位的结合亲和力。建议在B和T细胞表位预测工具中得分均高的表位。针对强毒NDV的肽疫苗大大取代了常规疫苗,因为它旨在涵盖变异的强毒突变株,从而将复发暴发及其巨大的伴随经济损失减少到最低限度。

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