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利用单克隆抗体6F4.D11.B6和8D6.B9.C3鉴定口蹄疫病毒O型病毒蛋白2上的保守线性表位

Identification of Conserved Linear Epitopes on Viral Protein 2 of Foot-and-Mouth Disease Virus Serotype O by Monoclonal Antibodies 6F4.D11.B6 and 8D6.B9.C3.

作者信息

Tommeurd Wantanee, Thueng-In Kanyarat, Theerawatanasirikul Sirin, Tuyapala Nongnaput, Poonsuk Sukontip, Petcharat Nantawan, Thangthamniyom Nattarat, Lekcharoensuk Porntippa

机构信息

Interdisciplinary Graduate Program in Genetic Engineering, The Graduate School, Kasetsart University, Bangkok 10900, Thailand.

School of Pathology, Translational Medicine Program, Institute of Medicine, Suranaree University of Technology, Nakhon Ratchasima 30000, Thailand.

出版信息

Antibodies (Basel). 2024 Aug 7;13(3):67. doi: 10.3390/antib13030067.

DOI:10.3390/antib13030067
PMID:39189238
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11348169/
Abstract

Foot-and-mouth disease (FMD) is a highly infectious disease of cloven-hoofed animals with a significant economic impact. Early diagnosis and effective prevention and control could reduce the spread of the disease which could possibly minimize economic losses. Epitope characterization based on monoclonal antibodies provide essential information for developing diagnostic assays and vaccine designs. In this study, monoclonal antibodies raised against FMD virus (FMDV) were produced. Sixty-six monoclonal antibodies demonstrated strong reactivity and specificity to FMDV. The purified monoclonal antibodies were further used for bio-panning to select phage expressing specific epitopes from phage-displayed 12 mer-peptide library. The phage peptide sequences were analyzed using multiple sequence alignment and evaluated by peptide ELISA. Two hybridoma clones secreted monoclonal antibodies recognizing linear epitopes on VP2 of FMDV serotype O. The non-neutralizing monoclonal antibody 6F4.D11.B6 recognized the residues 67-78 on antigenic site 2 resinding in VP2, while the neutralizing monoclonal antibody 8D6.B9.C3 recognized a novel linear epitope encompassing residues 115-126 on VP2. This information and the FMDV-specific monoclonal antibodies provide valuable sources for further study and application in diagnosis, therapeutics and vaccine designs to strengthen the disease prevention and control measures.

摘要

口蹄疫(FMD)是偶蹄动物的一种高度传染性疾病,具有重大经济影响。早期诊断以及有效的预防和控制可减少疾病传播,进而可能将经济损失降至最低。基于单克隆抗体的表位特征分析可为开发诊断检测方法和疫苗设计提供重要信息。在本研究中,制备了针对口蹄疫病毒(FMDV)的单克隆抗体。66种单克隆抗体对口蹄疫病毒表现出强反应性和特异性。纯化后的单克隆抗体进一步用于生物淘选,以从噬菌体展示的12肽文库中筛选表达特定表位的噬菌体。使用多序列比对分析噬菌体肽序列,并通过肽ELISA进行评估。两个杂交瘤克隆分泌识别口蹄疫病毒O型VP2上线性表位的单克隆抗体。非中和性单克隆抗体6F4.D11.B6识别VP2上抗原位点2中第67 - 78位残基,而中和性单克隆抗体8D6.B9.C3识别包含VP2上第115 - 126位残基的新型线性表位。这些信息以及口蹄疫病毒特异性单克隆抗体为进一步研究以及在诊断、治疗和疫苗设计中的应用提供了宝贵资源,以加强疾病预防和控制措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c55/11348169/0cbbad946af7/antibodies-13-00067-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c55/11348169/8f1befe0a046/antibodies-13-00067-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c55/11348169/2f7cd8443a43/antibodies-13-00067-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c55/11348169/e28cc070f491/antibodies-13-00067-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c55/11348169/98b5a3337535/antibodies-13-00067-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c55/11348169/0cbbad946af7/antibodies-13-00067-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c55/11348169/8f1befe0a046/antibodies-13-00067-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c55/11348169/2f7cd8443a43/antibodies-13-00067-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c55/11348169/e28cc070f491/antibodies-13-00067-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c55/11348169/98b5a3337535/antibodies-13-00067-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c55/11348169/0cbbad946af7/antibodies-13-00067-g005.jpg

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本文引用的文献

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Vaccines (Basel). 2023 Jun 18;11(6):1111. doi: 10.3390/vaccines11061111.
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Molecular evolution, diversity, and adaptation of foot-and-mouth disease virus serotype O in Asia.亚洲口蹄疫病毒O型的分子进化、多样性及适应性
Front Microbiol. 2023 Mar 9;14:1147652. doi: 10.3389/fmicb.2023.1147652. eCollection 2023.
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A Fc-enhanced NTD-binding non-neutralizing antibody delays virus spread and synergizes with a nAb to protect mice from lethal SARS-CoV-2 infection.
一种Fc增强的NTD结合非中和抗体可延缓病毒传播,并与一种中和抗体协同作用,保护小鼠免受致命的SARS-CoV-2感染。
Cell Rep. 2022 Feb 15;38(7):110368. doi: 10.1016/j.celrep.2022.110368. Epub 2022 Jan 25.
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Structural basis for SARS-CoV-2 neutralizing antibodies with novel binding epitopes.SARS-CoV-2 中和抗体的新型结合表位的结构基础。
PLoS Biol. 2021 May 7;19(5):e3001209. doi: 10.1371/journal.pbio.3001209. eCollection 2021 May.
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Detection of Bovine Antibodies against a Conserved Capsid Epitope as the Basis of a Novel Universal Serological Test for Foot-and-Mouth Disease.检测牛针对保守衣壳表位的抗体,作为口蹄疫新型通用血清学检测方法的基础。
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