非洲马病病毒肽疫苗的免疫信息学预测

Malaz Abdelbagi, Tarteel Hassan, Mohammed Shihabeldin, S. Bashir, Elkhaleel Ahmed, E. Mohamed, S. Hafiz, Abdah Abdelmonim, T. Hamid, S. Awad, A. Hamdi, Khoubieb Ali, Mohammed A Hassan
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引用次数: 11

摘要

背景:非洲马病是马科的一种病毒性疾病。它由吸血的库蚊蚊(Diptera,Ceratogonidae)传播,并在马身上引起严重疾病,可能导致死亡。非洲马疾病病毒(AHSV)是一种双链RNA(dsRNA)病毒,具有10个基因组片段,编码7种结构蛋白(VP1-VP7)和4种非结构蛋白(NS1、NS2、NS3、NS3A)。本研究的目的是分析国家生物技术中心信息数据库(NCBI)数据库中报告的非洲马病病毒(AHSV)株的VP2蛋白,以选择可用于设计肽疫苗的所有可能的表位。材料和方法:从国家生物技术中心信息数据库(NCBI)中检索到非洲马病病毒(AHSV)的27个外壳蛋白(VP2)序列(https://www.ncbi.nlm.nih.gov/蛋白质/?术语=VP2+非洲+马+疾病+病毒)。在它们身上,使用免疫表位分析数据库(IEDB)进行了几项测试,以检测B和T细胞的高度保守的免疫原性表位,从中选择所有可能用作治疗肽疫苗的表位。结果和讨论:关于将引发抗体免疫反应的表位,“FSPEYY、DKVVEDPSY和YDTDQNVV”被提议刺激B细胞。虽然每个MHC I和II的5个表位被认为是潜在的有前景的表位,因为它们结合了最高数量的等位基因,但所有这些表位都被发现在结构水平上与马MHC I类分子(ELA-A3)单倍型具有高结合亲和力和最低结合能“YAYCLILAL和YTFGNKFLL”之所以被代表,是因为它们与最多的等位基因结合。尽管与4个等位基因结合,但表位WFFDYYATL是有代表性的,因为它具有最低的全局能量。据我们所知,目前还没有使用计算机方法的基于表位的非洲马疾病病毒(AHSV)疫苗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunoinformatics Prediction of Peptide-Based Vaccine Against AfricanHorse Sickness Virus
Background: African horse sickness (AHS) is a viral disease of equidae. It is transmitted by hematophagous Culicoides midges (Diptera, Ceratopogonidae) and causes severe disease in horse that can lead to death. African Horse Sickness Virus (AHSV) is a double-stranded RNA (dsRNA) virus with ten genome segments encoding seven structural proteins (VP1-VP7) and four non-structural proteins (NS1, NS2, NS3, NS3A). The aim of this study is to analyze (VP2) protein of the African Horse Sickness Virus (AHSV) strains reported in the National Center for Biotechnology Information database (NCBI) database to select all possible epitopes that can be used to design a peptide vaccine. Materials and methods: A total of 27 outer capsid protein (VP2) sequences of African Horse Sickness Virus (AHSV) were retrieved from the National Center for Biotechnology Information database (NCBI) (https://www.ncbi.nlm. nih.gov/protein/?term=VP2+African+horse+sickness+virus) in the 7th of September 2016. On them, several tests were conducted using Immune Epitope Analysis Database (IEDB) to detect the highly conserved immunogenic epitopes of B and T cells from which all possible epitopes that can be used as a therapeutic peptide vaccine to be selected. Results and Discussion: Regarding epitopes that would elicit an antibody immune response, “FSPEYY, DKVVEDPESY and YDTDQNVV “were proposed to stimulate B cell. While 5 epitopes for each MHC I and II were addressed as potentially promising epitopes as they bound the highest number of alleles, all these epitopes were found to have a high binding affinity and the lowest binding energy to equine MHC class I molecule (ELA-A3) haplotype in the structural level. The epitopes “YAYCLILAL and YTFGNKFLL” were represented because they were bound to the largest number of alleles. In spite of binding to 4 alleles the epitope WFFDYYATL was represented because it has the lowest global energy. To our knowledge there is no epitope based vaccine for the African Horse Sickness Virus (AHSV) using in silico approaches.
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