In silico Prediction of Peptide based Vaccine against Fowlpox Virus (FPV)

Idris St, S. Salih, M. Basheir, A. Elhadi, S. Kamel, Abd-elrahman Ka, A. Hamdi, Mohammed A Hassan
{"title":"In silico Prediction of Peptide based Vaccine against Fowlpox Virus (FPV)","authors":"Idris St, S. Salih, M. Basheir, A. Elhadi, S. Kamel, Abd-elrahman Ka, A. Hamdi, Mohammed A Hassan","doi":"10.4172/1745-7580.1000154","DOIUrl":null,"url":null,"abstract":"Fowlpox virus (FPV) is double stranded DNA virus and a member of Poxviridae family which transmitted via aerosols and insect bite and causes cutaneous and diphtheritic infection in poultry population. This study aimed to design peptide vaccine by selecting all possible epitopes after analyzing of all FPV140 protein sequence reported in NCBI database using in silico approaches. After alignment of retrieved sequence the conserved region applied into IEDB analysis tool to predict B and T cell epitopes, then testing the affinity of predicted epitopes to bind to (BF2*2101) (BF2*0401) chicken receptor for MHC1 molecule, peptides low energy when docked against receptor were suggested as epitopes based vaccine. Peptides (50 PPSPKP 55, 51 PSPKPL 56, 52 SPKPLP 57, 53 PKPLPK 58, 54 KPLPKS 59, 55 PLPKSK 60, 56 LPKSKQ 61 and 18 RPSSTV 23) were most potential B cell epitopes while (110 YIMDNAEKL 118, 274 FYHRMYYPL 282, 278 MYYPLFSVF 286 231 YVVDNDRYV 239 and 317 LLSGVFLAY 325) docked epitopes suggested to be T cell epitopes because of their good binding affinity especially this overlapped one 110 YIMDNAEKL 118. This study concluded that those predicted epitopes might use to produce good vaccine against FPV after in vitro and in vivo studies to evaluate its efficiency.","PeriodicalId":73347,"journal":{"name":"Immunome research","volume":"14 1","pages":"1-11"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"9","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunome research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/1745-7580.1000154","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 9

Abstract

Fowlpox virus (FPV) is double stranded DNA virus and a member of Poxviridae family which transmitted via aerosols and insect bite and causes cutaneous and diphtheritic infection in poultry population. This study aimed to design peptide vaccine by selecting all possible epitopes after analyzing of all FPV140 protein sequence reported in NCBI database using in silico approaches. After alignment of retrieved sequence the conserved region applied into IEDB analysis tool to predict B and T cell epitopes, then testing the affinity of predicted epitopes to bind to (BF2*2101) (BF2*0401) chicken receptor for MHC1 molecule, peptides low energy when docked against receptor were suggested as epitopes based vaccine. Peptides (50 PPSPKP 55, 51 PSPKPL 56, 52 SPKPLP 57, 53 PKPLPK 58, 54 KPLPKS 59, 55 PLPKSK 60, 56 LPKSKQ 61 and 18 RPSSTV 23) were most potential B cell epitopes while (110 YIMDNAEKL 118, 274 FYHRMYYPL 282, 278 MYYPLFSVF 286 231 YVVDNDRYV 239 and 317 LLSGVFLAY 325) docked epitopes suggested to be T cell epitopes because of their good binding affinity especially this overlapped one 110 YIMDNAEKL 118. This study concluded that those predicted epitopes might use to produce good vaccine against FPV after in vitro and in vivo studies to evaluate its efficiency.
鸡痘病毒肽基疫苗的计算机预测
禽痘病毒(FPV)是一种双链DNA病毒,是痘病毒科的一员,通过气溶胶和昆虫叮咬传播,在家禽种群中引起皮肤和白喉感染。本研究通过对NCBI数据库中已报道的所有FPV140蛋白序列进行计算机分析,筛选出所有可能的表位,设计肽疫苗。将检索到的保守区序列进行比对,应用于IEDB分析工具预测B细胞和T细胞表位,并检测预测表位与MHC1分子(BF2*2101) (BF2*0401)鸡受体结合的亲和力,建议与受体对接时能量较低的肽段作为表位疫苗。肽(50 PPSPKP 55、51 PSPKPL 56、52 SPKPLP 57、53 PKPLPK 58、54 KPLPKS 59、55 PLPKSK 60、56 LPKSKQ 61和18 RPSSTV 23)是最潜在的B细胞表位,而(110 YIMDNAEKL 118、274 FYHRMYYPL 282、278 MYYPLFSVF 286、231 YVVDNDRYV 239和317 LLSGVFLAY 325)由于其良好的结合亲和力,特别是与110 YIMDNAEKL 118重叠,因此被认为是T细胞表位。本研究的结论是,这些预测的表位可能用于生产良好的FPV疫苗的体外和体内研究,以评估其有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信