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基于多表位的疫苗,通过靶向……的细胞黏附蛋白设计而成。 (原文此处不完整)

Multi-epitope-Based Vaccine Designed by Targeting Cytoadherence Proteins of .

作者信息

Mugunthan Susithra Priyadarshni, Harish Mani Chandra

机构信息

Plant Genetic Engineering and Molecular Farming Lab, Department of Biotechnology, Thiruvalluvar University, Serkkadu, Vellore 632115, Tamil Nadu, India.

出版信息

ACS Omega. 2021 May 17;6(21):13742-13755. doi: 10.1021/acsomega.1c01032. eCollection 2021 Jun 1.

DOI:10.1021/acsomega.1c01032
PMID:34095666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8173551/
Abstract

causes chronic respiratory disease in chickens leading to large economic losses in the poultry industry, and the impacts remain to be a great challenge for a longer period. Among the other approaches, a vaccine targeting the adhesion proteins of would be a promising candidate in controlling the infection. Thus, the present study is aimed to design a multi-epitope vaccine candidate using cytoadhesion proteins of through an advanced immunoinformatics approach. As a result, the multi-epitope vaccine was constructed, which comprised potential T-cell and B-cell binding epitopes with appropriate adjuvants. The designed multi-epitope vaccine represented high antigenicity with viable physiochemical properties. The prospective three-dimensional structure of the epitope was predicted, refined, and validated. The molecular docking analysis of multi-epitope vaccine candidates with the chicken Toll-like receptor-5 predicted effective binding. Furthermore, codon optimization and in silico cloning ensured high expression. Thus, the present finding indicates that the engineered multi-epitope vaccine is structurally stable and can induce a strong immune response. Furthermore, the multi-epitope vaccine is suggested to be a suitable vaccine candidate for the infection due to its effective binding capacity and precise specificity.

摘要

在鸡群中引发慢性呼吸道疾病,给家禽业造成巨大经济损失,且这种影响在较长时期内仍是巨大挑战。在其他方法中,针对[病原体名称]黏附蛋白的疫苗有望成为控制感染的候选方案。因此,本研究旨在通过先进的免疫信息学方法,利用[病原体名称]的细胞黏附蛋白设计一种多表位疫苗候选物。结果构建了多表位疫苗,其包含具有合适佐剂的潜在T细胞和B细胞结合表位。所设计的多表位疫苗具有高抗原性及可行的理化性质。预测、优化并验证了表位的三维结构。多表位疫苗候选物与鸡Toll样受体-5的分子对接分析预测了有效结合。此外,密码子优化和电子克隆确保了高表达。因此,本研究结果表明,工程化的多表位疫苗结构稳定,能诱导强烈免疫反应。此外,由于其有效的结合能力和精确的特异性,多表位疫苗被认为是针对[病原体名称]感染的合适疫苗候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/359b3ef77e67/ao1c01032_0012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/8670f962ca28/ao1c01032_0002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/ff6be49a8766/ao1c01032_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/cfcb89157a4a/ao1c01032_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/7e50d905435f/ao1c01032_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/e8b91995d5a5/ao1c01032_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/792aa7ae8360/ao1c01032_0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/696d4655d59a/ao1c01032_0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/359b3ef77e67/ao1c01032_0012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/8670f962ca28/ao1c01032_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/2c7e34e65b8b/ao1c01032_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/80e7ace212ee/ao1c01032_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/b1ff0d9b6545/ao1c01032_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/ff6be49a8766/ao1c01032_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/cfcb89157a4a/ao1c01032_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/7e50d905435f/ao1c01032_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/e8b91995d5a5/ao1c01032_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/792aa7ae8360/ao1c01032_0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/696d4655d59a/ao1c01032_0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2717/8173551/359b3ef77e67/ao1c01032_0012.jpg

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