马立克氏病病毒血清1型糖蛋白H和B多表位肽疫苗

S. Bashir, K. A. Abd-elrahman, Mohammed A Hassan, Yassir A. Almofti
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引用次数: 5

摘要

背景:马立克病(Marek 's disease, MD)是由马立克病病毒(Marek 's disease virus, MDV)引起的鸡的高度传染性疾病。它给家禽业造成的经济损失估计每年超过10亿美元。本研究的目的是设计一种针对马立克病病毒血清型1 (MDV-1)的肽疫苗,以糖蛋白H和B为免疫原,刺激保护性免疫反应。方法于2017年10月13日从美国国家生物技术信息中心数据库(NCBI)中检索到Gallid alphaherpesvirus 2 (MDV-1)糖蛋白H和糖蛋白B各43份。免疫表位数据库(IEDB)的几种检测方法用于检测高度保守的免疫原性表位,这些表位可引发B细胞和T细胞,并可作为有效的候选疫苗。在我们的结果中,糖蛋白H的三个表位分别是;91-FYKRPVSKLL-100、255-LKPYEPVDKF-264和684-PRPL-687以及糖蛋白B的三个表位;162- EKQV-165、234-YGLSPPE-240和363-YNDSHVK-369符合表面可及性、抗原性标准,成为最可能的B细胞表位。糖蛋白H的四个表位;425-YVLRSAYAF-433、175-LTSELTGTY-183、476-LYYAFASIF-484和367-MITETLSTF-375在结构水平上结合MHC-I和MHC-II等位基因数量最多,与鸡MHC-I分子(BF2*2101)单倍型具有高结合亲和力,因此被认为是有潜力的表位。糖蛋白B也有两个表位;598-FLFGSGYAL-606、727-FMSNPFGAL-735与MHC-I和MHC-II的结合数量最多,具有较高的结合亲和力。马立克氏病是一种重要的家禽疾病。我们从糖蛋白H和B中找到了可以作为候选疫苗的表位。据我们所知,目前还没有针对马立克病病毒血清型1 (mdv1)的基于硅表位的疫苗。需要体外和体内应用来证明预测的表位作为肽疫苗的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi Epitope Based Peptide Vaccine against Marek’s Disease Virus Serotype 1 Glycoprotein H and B
Background: Marek’s disease (MD) is a highly contagious disease of chickens caused by Marek’s disease virus (MDV). It causes economic losses in poultry industry estimated to be more than 1 billion per year. The aim of this study was to design a peptide vaccine against Marek’s disease virus serotype 1 (MDV-1) by targeting the Glycoproteins H and B as an immunogens to stimulate protective immune response. A total of 43 Glycoprotein H and 33 glycoprotein B of Gallid alphaherpesvirus 2 (MDV-1) were retrieved from the National Center for Biotechnology Information database (NCBI) in the 13th of October 2017. Several tests at Immune Epitope Database (IEDB) were used to detect the highly conserved immunogenic epitopes that elicit B and T cells and could be used as efficient vaccine candidates. In our results three epitopes from glycoprotein H namely; 91-FYKRPVSKLL-100, 255-LKPYEPVDKF-264, and 684-PRPL-687 and three epitopes of glycoprotein B; 162- EKQV-165, 234-YGLSPPE-240, and 363-YNDSHVK-369 were fulfilled the criteria of surface accessibility, antigenicity for becoming the most probable B cell epitope. While Four epitopes of glycoprotein H; 425-YVLRSAYAF-433, 175-LTSELTGTY-183, 476-LYYAFASIF-484, and 367-MITETLSTF-375 were addressed as potentially promising epitopes as they bound the highest number of both MHC-I and MHC-II alleles with a high binding affinity to chickens MHC-I molecule (BF2*2101) haplotype in the structural level. Also two epitopes of glycoprotein B; 598-FLFGSGYAL-606, 727-FMSNPFGAL-735 were bound with the highest number of both MHC-I and MHC-II with high binding affinity. Taken together Marek’s disease is a significant disease of poultry. We addressed epitopes from glycoprotein H and B that could act as candidates’ vaccine. To our knowledge there is no in silico epitope based vaccine for Marek’s disease virus serotype 1 (MDV-1). An in vitro and in vivo application is required to prove the efficacy of the predicted epitopes as peptide vaccine.
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