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制备并鉴定针对口蹄疫病毒 O 型血清型的单克隆抗体,并建立一种用于病毒抗原检测的夹心 ELISA 方法。

Production and characterization of monoclonal antibodies against foot-and-mouth disease virus serotype O and development of a sandwich ELISA for virus antigen detection.

机构信息

ICAR-Directorate of Foot and Mouth Disease-International Centre for FMD, Bhubaneswar, Khordha, Odisha, 752050, India.

出版信息

Vet Res Commun. 2023 Dec;47(4):1915-1924. doi: 10.1007/s11259-023-10143-9. Epub 2023 May 24.

Abstract

Foot-and-mouth disease (FMD) is endemic in India with a majority of outbreaks caused by FMD virus (FMDV) serotype O. In the present study a panel of eight (2F9, 2G10, 3B9, 3H5, 4C8, 4D6, 4G10 and 5B6) mouse monoclonal antibodies (MAbs) were developed against FMDV serotype O Indian vaccine strain, O/IND/R2/75 via hybridoma systems. The MAbs generated were FMDV/O specific without cross-reactivity against FMDV type A and Asia 1. All the MAbs were identified as IgG1/kappa type. Out of eight, three MAbs (3B9, 3H5 and 4G10) demonstrated virus neutralizing activity. The reactivity of all MAbs increased with heat treated (@56C) serotype O antigen compared to untreated antigen in sandwich ELISA indicating that their binding epitopes are linear. Six MAbs (except 2F9 and 4D6) reacted with recombinant P1 protein of homologous virus in an indirect ELISA among which only MAb 3B9 bound to VP1. MAb profiling of 37 serotype O field viruses isolated between the years 1962 and 2021 demonstrated antigenic similarity between field isolates and reference vaccine strain. MAbs 5B6 and 4C8 consistently reacted with all 37 isolates. In indirect immunofluorescence assay MAb 5B6 bound well with FMDV/O antigen. Finally, a sandwich ELISA was successfully developed using rabbit polyclonal anti-FMDV/O serum and MAb 5B6 for detection of FMDV/O antigen in clinical samples (n = 649). The new assay exhibited 100% and 98.89% diagnostic sensitivity and specificity respectively compared to traditional polyclonal antibody-based sandwich ELISA suggesting that the MAb-based ELISA developed here could be an effective method for detection of FMDV serotype O.

摘要

口蹄疫(FMD)在印度流行,大多数疫情是由 FMD 病毒(FMDV)血清型 O 引起的。在本研究中,通过杂交瘤系统,针对 FMDV 血清型 O 印度疫苗株 O/IND/R2/75,开发了 8 株(2F9、2G10、3B9、3H5、4C8、4D6、4G10 和 5B6)鼠单克隆抗体(MAb)。产生的 MAb 对 FMDV/O 具有特异性,与 FMDV 型 A 和 Asia 1 无交叉反应。所有 MAb 均鉴定为 IgG1/κ 型。在 8 株中,有 3 株 MAb(3B9、3H5 和 4G10)具有病毒中和活性。与未经处理的抗原相比,所有 MAb 在夹心 ELISA 中与热处理(@56°C)的血清型 O 抗原的反应性增加,表明它们的结合表位是线性的。6 株 MAb(除 2F9 和 4D6 外)在间接 ELISA 中与同源病毒的重组 P1 蛋白反应,其中只有 MAb 3B9 与 VP1 结合。对 1962 年至 2021 年间分离的 37 株血清型 O 田间病毒的 MAb 分析表明,田间分离株与参考疫苗株之间具有抗原相似性。MAb 5B6 和 4C8 始终与所有 37 个分离株反应。在间接免疫荧光测定中,MAb 5B6 与 FMDV/O 抗原结合良好。最后,使用兔多克隆抗 FMDV/O 血清和 MAb 5B6 成功开发了夹心 ELISA,用于检测临床样本中的 FMDV/O 抗原(n=649)。与传统的基于多克隆抗体的夹心 ELISA 相比,新的测定法的诊断敏感性和特异性分别为 100%和 98.89%,表明这里开发的 MAb 基于 ELISA 可能是检测 FMDV 血清型 O 的有效方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d09e/10206340/b9307d6b3546/11259_2023_10143_Fig1_HTML.jpg

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