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设计一种针对鸭疫里默氏杆菌的多表位复合疫苗候选物:一项计算机模拟研究。

Designing a polytopic complex vaccine candidate against Gallibacterium anatis: an In-silico study.

作者信息

Ataei S, Ranjbar M M, Motamed N, Ataei Kachooei S, Amini Njafi F

机构信息

Department of Avian Bacterial Diseases, Razi Vaccine and Serum Research Institute, Agricultural Research, Education, and Extension Organization, Karaj, Iran.

Department of Animal Viral Diseases, Razi Vaccine and Serum Research Institute, Agricultural Research, Education, and Extension Organization, Karaj, Iran.

出版信息

Arch Razi Inst. 2019 Mar;74(1):7-20. doi: 10.22092/ari.2017.109804.1118. Epub 2019 Mar 1.

Abstract

The haemolytic biovar of Gallibacterium anatis (G. anatis) is responsible for urogenital, gastrointestinal, and respiratory diseases in chickens. There are numerous reports on the resistance of G. anatis to antibiotics and recurrence of the disease, which raise concerns about antimicrobial treatment efficiency. Vaccination has been considered as the most feasible procedure of prevention in high risk farms. Subunit vaccines containing immunogenic components can have practical protective value in preventive measures regarding the infection. The present study aimed to introduce a polytopic vaccine candidate based on epitope detection. All registered sequences of four immunogenic proteins, includig Flfa, GTxA, Gab_1309, and Gab_2348 were retrieved and directed for variational analysis. A vaccine isolate was selected for each protein and tested for B-cell epitope mapping using different tools. Furthermore, consensus selected immunogenic regions with special patterns fused together by flexible linkers were integrated into two constructs and checked for the best status of proteasomal cleavage sites, as well as hydropathy plot. Moreover, back translations, along with codon optimization were performed, and then some tags were added to the constructs. The selected consensus B-cell immunogenic epitopes were for 12656: AA114-181, 7990: AA114-181, Avicor: AA42-77, 134-197, and IPDH: 61-155 for Flfa protein, AA185-235, AA372-457, and AA807-941 for GtxA-N, AA260-305, AA340-400, and AA110-146 for Gab-1309, and AA125-AA175 for Gab-2348. Two suitable patterns of attachment were selected from the different fusion patterns of epitopes in B-cell polytopic vaccinal constructs. Finally, the examination of these constructs showed their effect and efficacy for immune system stimulation. Based on bioinformatics results, these immunogens could be utilized as potential candidates to develop polytopic protective vaccines and design diagnostic kits.

摘要

鸭源鸡杆菌(G. anatis)的溶血型生物变种可引发鸡的泌尿生殖系统、胃肠道和呼吸系统疾病。关于鸭源鸡杆菌对抗生素的耐药性以及疾病复发的报道众多,这引发了人们对抗菌治疗效果的担忧。在高风险养殖场,疫苗接种被视为最可行的预防措施。含有免疫原性成分的亚单位疫苗在预防感染方面具有实际的保护价值。本研究旨在基于表位检测引入一种多位点疫苗候选物。检索了四种免疫原性蛋白(包括Flfa、GTxA、Gab_1309和Gab_2348)的所有已注册序列,并进行变异分析。为每种蛋白选择了一种疫苗分离株,并使用不同工具对其进行B细胞表位图谱分析。此外,将通过柔性接头融合在一起的具有特殊模式的共有选择免疫原性区域整合到两个构建体中,并检查蛋白酶体切割位点的最佳状态以及亲水性图谱。此外,进行了反向翻译和密码子优化,然后在构建体上添加了一些标签。所选的共有B细胞免疫原性表位为:Flfa蛋白的12656:AA114 - 181、7990:AA114 - 181、Avicor:AA42 - 77、134 - 197以及IPDH:61 - 155;GtxA - N的AA185 - 235、AA372 - 457以及AA807 - 941;Gab - 1309的AA260 - 305、AA340 - 400以及AA110 - 146;Gab - 2348的AA125 - AA175。从B细胞多位点疫苗构建体中表位的不同融合模式中选择了两种合适的连接模式。最后,对这些构建体的检测显示了它们对免疫系统刺激的效果和功效。基于生物信息学结果,这些免疫原可作为开发多位点保护性疫苗和设计诊断试剂盒的潜在候选物。

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