Chen Wenting, Yang Jifei, Niu Qingli, Wang Jinming, Liu Yanghe, Li Xuesai, Zhao Yaru, Zhang Zhonghui, Liu Zhijie, Guan Guiquan, Yin Hong
State Key Laboratory for Animal Disease Control and Prevention, African Swine Fever Regional Laboratory of China (Lanzhou), Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Xujiaping 1, Lanzhou, 730046, Gansu, P. R. China.
Institute of Special Animal and Plant Sciences, Chinese Academy of Agricultural Sciences, Changchun, 130112, P. R. China.
Virol J. 2025 Jun 5;22(1):182. doi: 10.1186/s12985-025-02781-z.
African swine fever (ASF) is a highly infectious and devastating disease that poses a significant threat to the global swine industry. The rapid spread of ASF and its ongoing pandemics continue to impact pig farming worldwide. The absence of an effective vaccine, coupled with the complexity of the African swine fever virus (ASFV), makes the control and eradication of ASF a formidable challenge. Nanobodies, derived from camelids, have emerged as promising alternatives to conventional monoclonal antibodies, offering distinct advantages in various biological applications. In this study, specific nanobodies targeting the ASFV K205R protein were selected from a phage-displayed immune library. Ten individual nanobodies were isolated based on their complementary determining regions (CDRs), and four were found to bind to the naive K205R protein of ASFV. After evaluation, nanobody VHH1 was selected for the development of a competitive enzyme-linked immunosorbent assay (ELISA) for ASFV antibody detection. The assay was optimized for various reaction conditions, and the cut-off value was determined to be 26.85%, with diagnostic sensitivity and specificity of 97.52% and 97.48%, respectively. No cross-reactivity was observed with sera from pigs infected with other swine viruses, and the assay exhibited a detection sensitivity of 1:128. Comparative analysis of clinical samples showed a high concordance rate (98.98%) between the nanobody-based and monoclonal antibody-based ELISAs (Mab-cELISA). In conclusion, this study presents a phage-displayed nanobody-based competitive ELISA for the detection of ASFV antibodies, which could be valuable for ASF sero-surveillance. Additionally, the K205R-specific nanobodies identified here may be adapted for other biological or biomedical applications.
非洲猪瘟(ASF)是一种极具传染性和毁灭性的疾病,对全球养猪业构成重大威胁。ASF的迅速传播及其持续的大流行继续影响着全球的养猪业。由于缺乏有效的疫苗,再加上非洲猪瘟病毒(ASFV)的复杂性,使得ASF的控制和根除成为一项艰巨的挑战。源自骆驼科动物的纳米抗体已成为传统单克隆抗体的有前途的替代品,在各种生物学应用中具有明显优势。在本研究中,从噬菌体展示免疫文库中筛选出针对ASFV K205R蛋白的特异性纳米抗体。基于互补决定区(CDR)分离出10个单个纳米抗体,发现其中4个与ASFV的天然K205R蛋白结合。经过评估,选择纳米抗体VHH1用于开发用于检测ASFV抗体的竞争性酶联免疫吸附测定(ELISA)。对各种反应条件进行了优化,确定临界值为26.85%,诊断敏感性和特异性分别为97.52%和97.48%。未观察到与感染其他猪病毒的猪血清发生交叉反应,该测定的检测灵敏度为1:128。临床样本的比较分析表明,基于纳米抗体的ELISA和基于单克隆抗体的ELISA(Mab-cELISA)之间的一致性率很高(98.98%)。总之,本研究提出了一种基于噬菌体展示纳米抗体的竞争性ELISA用于检测ASFV抗体,这对ASF血清监测可能具有重要价值。此外,此处鉴定的K205R特异性纳米抗体可能适用于其他生物学或生物医学应用。