Production and Characterization of Monoclonal Antibodies Against the VP7 Protein of Epizootic Hemorrhagic Disease Virus.

Q3 Medicine
Gisella Armillotta, Tiziana Di Febo, Simonetta Ulisse, Caterina Laguardia, Mariangela Iorio, Ivanka Krasteva, Manuela Tittarelli, Maria Teresa Mercante, Mirella Luciani
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引用次数: 1

Abstract

Monoclonal antibodies (MAbs) against epizootic hemorrhagic disease virus (EHDV) were produced by immunizing BALB/c mice with rec-VP7-EHDV2; 66 clones producing MAbs able to recognize the VP7-EHDV with a strong reaction were obtained and tested in indirect enzyme-linked immunosorbent assay (i-ELISA) against the whole epizootic hemorrhagic disease (EHD) virus serotype 2; potential cross-reactions with related orbiviruses, as Bluetongue virus (BTV) and African horse sickness virus (AHSV), were investigated as well by i-ELISA, Western blot, and immunofluorescence. Fifty-three MAbs were specific for EHDV (VP7 recombinant protein and whole virus) and 13 reacted also with the VP7 of BTV. None of the MAbs reacted with AHSV. MAbs specific for EHDV were further characterized in a competitive ELISA (c-ELISA): 20 among them were found useful to develop a c-ELISA for the detection of antibodies against EHDV in bovine sera. The availability of this extensive set of MAbs provides the opportunity to develop a c-ELISA for the serological diagnosis of EHDV and to tune new methods for the isolation and identification of the virus in biological samples and cell cultures. The experimentation protocol was approved by the Italian Ministry of Health (number 639/2018-PR, Resp. to Prot. BDF16.13#295833199#).

动物流行性出血病病毒VP7蛋白单克隆抗体的制备与鉴定
用rec-VP7-EHDV2免疫BALB/c小鼠制备抗动物流行性出血病病毒(EHDV)的单克隆抗体;本文获得了66个克隆,克隆产生的单克隆抗体能够识别VP7-EHDV并产生强烈反应,并用间接酶联免疫吸附试验(i-ELISA)对2型EHD病毒进行了检测;利用i-ELISA、Western blot和免疫荧光技术研究了其与蓝舌病病毒(BTV)和非洲马病病毒(AHSV)等相关病毒的潜在交叉反应。53个单抗对EHDV (VP7重组蛋白和全病毒)具有特异性,13个单抗也能与BTV的VP7反应。这些单克隆抗体均未与AHSV发生反应。在竞争性ELISA (c-ELISA)中进一步对EHDV特异性单克隆抗体进行了鉴定,发现其中20个单克隆抗体可用于开发检测牛血清中EHDV抗体的c-ELISA。这组广泛的单克隆抗体的可用性为开发用于EHDV血清学诊断的c-ELISA提供了机会,并调整了在生物样品和细胞培养物中分离和鉴定病毒的新方法。实验方案已获得意大利卫生部批准(编号639/2018-PR, Resp。来保护。BDF16.13 # 295833199 #)。
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来源期刊
CiteScore
4.80
自引率
0.00%
发文量
49
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