Xu Zhihao, Liu Man, He Qiyi, Li Wenkai, Pan Junkang, El-Sheikh El-Sayed A, Liu Wenzhi, Hammock Bruce D, Li Dongyang
College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou, 310058, People's Republic of China; Zhejiang Key Laboratory of Intelligent Sensing and Robotics for Agriculture, Hangzhou, 310058, People's Republic of China.
Yangtze River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Wuhan, 430223, People's Republic of China.
Anal Chim Acta. 2025 May 8;1350:343877. doi: 10.1016/j.aca.2025.343877. Epub 2025 Feb 26.
Aquatic viruses cause devastating diseases in aquaculture, severely limiting production and resulting in significant economic losses. The giant salamander iridovirus (GSIV), a member of the genus Ranavirus, is the only virus reported to infect giant salamanders, posing a severe threat to the farming industry. Currently, there are no effective strategies available for its control. In this context, a reliable diagnostic tool for the rapid detection of GSIV is crucial to mitigate its impact. This study developed a nanobody-based immunoassay for the rapid and reliable detection of GSIV. GSIV was cultured and used to immunize an alpaca, A phage library with an original diversity of 1.89 × 10 PFU was established, and six nanobodies were identified after three rounds of panning. Among them, HC-2 exhibited superior performance and was used to develop a highly sensitive ELISA method employing streptavidin-PolyHRP (SA-PolyHRP) as a signal amplification strategy. The assay achieved a detection limit of 3.3 × 10 PFU/mL and demonstrated high specificity without cross-reactivity. Practical application was validated in infected giant salamander samples, underscoring its diagnostic potential. This work provides a robust tool for GSIV diagnosis and showcases the potential of nanobodies in advancing aquaculture diagnostics.
水生病毒在水产养殖中引发毁灭性疾病,严重限制产量并导致重大经济损失。大鲵虹彩病毒(GSIV)是蛙病毒属的成员,是唯一有报道感染大鲵的病毒,对养殖业构成严重威胁。目前,尚无有效的控制策略。在此背景下,一种用于快速检测GSIV的可靠诊断工具对于减轻其影响至关重要。本研究开发了一种基于纳米抗体的免疫测定法,用于快速、可靠地检测GSIV。培养GSIV并用其免疫羊驼,建立了原始多样性为1.89×10 PFU的噬菌体文库,经过三轮淘选后鉴定出6种纳米抗体。其中,HC-2表现出优异性能,并被用于开发一种以链霉亲和素-聚辣根过氧化物酶(SA-PolyHRP)作为信号放大策略的高灵敏度ELISA方法。该测定法的检测限达到3.3×10 PFU/mL,具有高特异性且无交叉反应性。在感染大鲵的样本中验证了其实际应用,突出了其诊断潜力。这项工作为GSIV诊断提供了一种强大的工具,并展示了纳米抗体在推进水产养殖诊断方面的潜力。