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通过适体-衣壳蛋白-适体夹心酶联适体吸附测定法(ELASA)快速灵敏地检测红斑石斑鱼神经坏死病毒(RGNNV)感染

Rapid and sensitive detection of redspotted grouper nervous necrosis virus (RGNNV) infection by aptamer-coat protein-aptamer sandwich enzyme-linked apta-sorbent assay (ELASA).

作者信息

Zhou L, Li P, Ni S, Yu Y, Yang M, Wei S, Qin Q

机构信息

Key Laboratory of Tropical Marine Bio-resources and Ecology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou, China.

University of Chinese Academy of Sciences, Beijing, China.

出版信息

J Fish Dis. 2017 Dec;40(12):1831-1838. doi: 10.1111/jfd.12656. Epub 2017 Jul 26.

Abstract

Redspotted grouper nervous necrosis virus (RGNNV) is one of the most devastating pathogens in the aquaculture of the grouper, Epinephlus sp., worldwide. The early and rapid diagnosis of RGNNV is important for the prevention of RGNNV infection. In this study, an aptamer (A10)-based sandwich enzyme-linked apta-sorbent assay (ELASA) was developed for RGNNV diagnosis. This sandwich ELASA showed high specificity for the RGNNV coat protein (CP) and virions in virus-infected cells and tissues. At the optimized working concentration of 200 nM of aptamer, the ELASA could detect RGNNV in the lysates of as few as 4 × 10 RGNNV-infected GB cells. Incubation for 10 min was sufficient to produce accurate results. The sandwich ELASA was most stable at incubation temperatures of 4-25°C, but could still distinguish RGNNV-infected samples from the controls at 37°C. It could detect RGNNV infection in brain lysates diluted 1/10, with results consistent with those of reverse transcription PCR, although with 10% less sensitivity. The main equipment required includes dissection tools, a water bath, Pierce™ Streptavidin Coated Plates and a microplate reader. The sandwich ELASA has great potential utility for the rapid and sensitive diagnosis of RGNNV in its early stages by fish farmers.

摘要

红斑石斑鱼神经坏死病毒(RGNNV)是全球石斑鱼(Epinephlus sp.)水产养殖中最具毁灭性的病原体之一。RGNNV的早期快速诊断对于预防RGNNV感染至关重要。在本研究中,开发了一种基于适体(A10)的夹心酶联适体吸附测定法(ELASA)用于RGNNV诊断。这种夹心ELASA对病毒感染细胞和组织中的RGNNV衣壳蛋白(CP)和病毒粒子具有高度特异性。在适体优化工作浓度为200 nM时,ELASA能够检测低至4×10个被RGNNV感染的GB细胞裂解物中的RGNNV。孵育10分钟足以产生准确结果。夹心ELASA在4 - 25°C孵育温度下最稳定,但在37°C时仍能区分被RGNNV感染的样品和对照。它能够检测稀释1/10的脑裂解物中的RGNNV感染,结果与逆转录PCR一致,尽管灵敏度低10%。所需的主要设备包括解剖工具、水浴、Pierce™链霉亲和素包被板和酶标仪。这种夹心ELASA在早期为养鱼户快速灵敏诊断RGNNV方面具有巨大的潜在应用价值。

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