Department of Preventive Veterinary Medicine, College of Veterinary Medicine, Northwest A&F University; Yangling Observing and Experimental Station of National Data Center of Animal Health, Ministry of Agriculture, Yangling, 712100, China.
Kunming Customs Technology Center, Kunming, 650228, China.
Virol Sin. 2022 Dec;37(6):922-933. doi: 10.1016/j.virs.2022.09.004. Epub 2022 Sep 8.
African swine fever virus (ASFV) infection is a big threat to the global pig industry. Because there is no effective vaccine, rapid, low-cost, and simple diagnosis methods are necessary to detect the ASFV infection in pig herds. Nanobodies, with advantages of small molecular weight and easy genetic engineering, have been universally used as reagents for developing diagnostic kits. In this study, the recombinant ASFV-p30 was expressed and served as an antigen to immunize the Bactrian camel. Then, seven nanobodies against ASFV-p30 were screened using phage display technique. Subsequently, the seven nanobodies fused horseradish peroxidase (nanobody-HRP) were secretory expressed and one fusion protein ASFV-p30-Nb75-HRP was selected with the highest sensitivity in blocking ELISA. Using the ASFV-p30-Nb75-HRP fusion protein as a probe, a competitive ELISA (cELISA) was developed for detecting anti-ASFV antibodies in pig sera. The cut-off value of cELISA was determined to be 22.7% by testing 360 negative pig sera. The detection limit of the cELISA for positive pig sera was 1:320, and there was no cross-reaction with anti-other swine virus antibodies. The comparative assay showed that the agreement of the cELISA with a commercial ELISA kit was 100%. More importantly, the developed cELISA showed low cost and easy production as a commercial kit candidate. Collectively, a simple nanobody-based cELISA for detecting antibodies against ASFV is developed and it provides a new method for monitoring ASFV infection in the pig herds.
非洲猪瘟病毒(ASFV)感染对全球养猪业构成了巨大威胁。由于目前尚无有效的疫苗,因此需要快速、低成本且简单的诊断方法来检测猪群中的 ASFV 感染。纳米抗体具有分子量小和易于基因工程改造的优势,已被广泛用作开发诊断试剂盒的试剂。本研究中,表达了重组 ASFV-p30 作为抗原,对双峰驼进行了免疫。然后,使用噬菌体展示技术筛选了针对 ASFV-p30 的七个纳米抗体。随后,将七个纳米抗体融合辣根过氧化物酶(nanobody-HRP)进行分泌表达,并通过阻断 ELISA 筛选出具有最高灵敏度的融合蛋白 ASFV-p30-Nb75-HRP。使用 ASFV-p30-Nb75-HRP 融合蛋白作为探针,建立了用于检测猪血清中抗 ASFV 抗体的竞争 ELISA(cELISA)。通过检测 360 份阴性猪血清,确定 cELISA 的截断值为 22.7%。cELISA 对阳性猪血清的检测限为 1:320,与抗其他猪病毒抗体无交叉反应。比较试验表明,cELISA 与商业 ELISA 试剂盒的一致性为 100%。更重要的是,所开发的 cELISA 具有成本低、易于生产等优点,可作为商业试剂盒的候选。总之,本研究开发了一种简单的基于纳米抗体的 cELISA 来检测抗 ASFV 的抗体,为监测猪群中的 ASFV 感染提供了新方法。