Key Laboratory of Jiangsu Preventive Veterinary Medicine, Ministry of Education, College of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Key Laboratory for Avian Preventive Medicine, Ministry of Education, College of Veterinary Medicine, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Appl Microbiol Biotechnol. 2022 Jan;106(2):855-863. doi: 10.1007/s00253-021-11711-2. Epub 2021 Dec 18.
The outbreak of goose gout disease caused by novel goose astrovirus type 1 (GAstV-1) has resulted in huge economic losses to the goose industry in China since 2017. However, little is known about the B cell epitopes in major antigen of GAstV-1 and the serological approach for detection of GAstV-1 is not available. In this study, three novel monoclonal antibodies (mAbs) against the ORF2 protein were first generated and designated as 3G6, 5H7, and 6C6, respectively. Epitope mapping revealed that mAb 3G6, 5H7, and 6C6 recognized AVRFEKGGHE, EKALSAPQAG, and DDDPLSDVTS in ORF2, respectively. Sequence alignments found that the three epitopes were highly conserved in GAstV-1 but not in other AAstV members. Moreover, a mAb-based sandwich ELISA for the detection of GAstV-1 was first developed using mAb 6C6. The sandwich ELISA only reacted with GAstV-1 but not with GAstV-2 and the other goose-associated viruses tested. The limit of the detection of the sandwich ELISA reaches 1.58 × 10 TCID/mL of GAstV-1. Notably, mAb 6C6 could also efficiently react with the GAstV-1 in tissue frozen sections of the clinical infected goose through IFA. The mAbs generated in this study pave the way for further studying on the role of ORF2 in the infection and pathogenesis of GAstV, and the sandwich ELISA and the tissue frozen section-IFA approaches established here provide efficient and rapid serological diagnostic tools for detection of GAstV-1. KEY POINTS: • Three novel B cell epitopes were identified in ORF2 of GAstV-1. • mAb-based ELISA and IFA for detection of GAstV-1 were developed.
自 2017 年以来,新型鹅星状病毒 1 型(GAstV-1)引起的鹅痛风病爆发给中国养鹅业造成了巨大的经济损失。然而,人们对 GAstV-1 的主要抗原中的 B 细胞表位知之甚少,并且目前还没有用于检测 GAstV-1 的血清学方法。在本研究中,首次针对 ORF2 蛋白生成了三种新型单克隆抗体(mAb),并分别命名为 3G6、5H7 和 6C6。表位作图显示,mAb 3G6、5H7 和 6C6 分别识别 ORF2 中的 AVRFEKGGHE、EKALSAPQAG 和 DDDPLSDVTS。序列比对发现,这三个表位在 GAstV-1 中高度保守,但在其他 AAstV 成员中则不然。此外,首次使用 mAb 6C6 建立了用于检测 GAstV-1 的基于 mAb 的夹心 ELISA。夹心 ELISA 仅与 GAstV-1 反应,而不与 GAstV-2 和测试的其他鹅相关病毒反应。夹心 ELISA 的检测限达到 1.58×10 TCID/mL 的 GAstV-1。值得注意的是,mAb 6C6 还可以通过 IFA 有效地与临床感染鹅组织冷冻切片中的 GAstV-1 反应。本研究中生成的 mAb 为进一步研究 ORF2 在 GAstV 感染和发病机制中的作用铺平了道路,并且这里建立的夹心 ELISA 和组织冷冻切片-IFA 方法为检测 GAstV-1 提供了高效快速的血清学诊断工具。关键点: • 在 GAstV-1 的 ORF2 中鉴定出三个新的 B 细胞表位。 • 建立了基于 mAb 的 ELISA 和 IFA 用于检测 GAstV-1。