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利用高分辨率熔解曲线分析区分草鱼出血病病毒基因型 II 的疫苗株和野毒株。

Use of high-resolution melting curve analysis to differentiate vaccine and wild type strains of grass carp reovirus genotype II.

机构信息

College of Medical Science and Technology, Heze University, Heze 274015, Shandong, China.

Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Key Laboratory of Fishery Drug Development, Ministry of Agriculture, Key Laboratory of Aquatic Animal Immune Technology, Guangzhou 510380, Guangdong, China.

出版信息

J Virol Methods. 2018 Jun;256:111-115. doi: 10.1016/j.jviromet.2018.03.006. Epub 2018 Mar 17.

Abstract

Grass carp reovirus (GCRV) is the causative agent of a hemorrhagic disease that causes severe economic losses in the grass carp (Ctenopharyngodon idella) farming industry in China. Discrimination between wild-type field and vaccine strains of GCRV is crucial for meaningful disease diagnosis and epidemiological investigation, yet current detection methods do not discriminate between these different viruses. This study exploited sequence differences between vaccine viruses and the virulent and field strains in the S6 gene that is present in all GCRV strains to develop a high resolution melting curve assay to differentiate between virus strains. The high resolution melting curve analysis was as analytically sensitive as real-time quantitative-Polymerase Chain Reaction (qPCR) detection and at least 10 times sensitive than the conventional PCR. This one-step assay will facilitate grass carp hemorrhagic disease outbreak responses and control.

摘要

草鱼出血病是由草鱼出血病病毒(GCRV)引起的,这种病毒在中国草鱼养殖业中导致了严重的经济损失。区分野生型田间株和 GCRV 疫苗株对于有意义的疾病诊断和流行病学调查至关重要,但目前的检测方法无法区分这些不同的病毒。本研究利用 S6 基因中疫苗株与强毒和田间株之间的序列差异,开发了一种高分辨率熔解曲线分析方法,以区分病毒株。高分辨率熔解曲线分析在分析灵敏度上与实时定量聚合酶链反应(qPCR)检测相当,比常规 PCR 至少灵敏 10 倍。这种一步法检测将有助于草鱼出血病暴发的应对和控制。

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