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当前位置: 首页 > 文章 > 传染性造血器官坏死病毒环介导等温扩增检测方法的建立和初步应用 淡水渔业 2019,49 (3) 66-70
Position: Home > Articles > Establishment and preliminary application of loop-mediated isothermal amplification for detection of infectious haematopoietic necrosis virus Freshwater Fisheries 2019,49 (3) 66-70

传染性造血器官坏死病毒环介导等温扩增检测方法的建立和初步应用

作  者：
何亚鹏;陈怡静;时晓;张宝莉;温战华;陈春山;李博;杜迎春
单  位：
郑州外国语新枫杨学校;北京市水生野生动植物救护中心
关键词：
传染性造血器官坏死病毒;鲑鳟;环介导等温扩增;核蛋白基因
摘  要：
实验建立了一套反转录环介导等温扩增方法(reverse transcription loop-mediated isothermal amplification,RT-LAMP),用于实验室及现场检测鲑鳟鱼传染性造血器官坏死病毒(infectious haematopoietic necrosis virus,IHNV).针对IHNV的核蛋白基因设计特异性引物,以IHNV基因组RNA为模板,在反转录酶及Bst DNA聚合酶的作用下进行反转录LAMP,结果阳性样本表现为荧光绿色,阴性样本仍为红棕色.反应条件优化结果表明最适反应温度为64℃;特异性试验表明仅IHNV发生特异性扩增,而SVCV、HRV、VHSV和H2 O均不发生反应;敏感性试验表明该LAMP方法可检出浓度为1.0×10-4μg/μL的IHNV核酸.本研究所建立的IHNV反转录LAMP检测法成本低、 操作简单、 反应迅速、 不依赖专门的仪器,同时具有较高的灵敏度和特异性,适合IHNV的现场检测和大批量样品的检疫.
译  名：
Establishment and preliminary application of loop-mediated isothermal amplification for detection of infectious haematopoietic necrosis virus
作  者：
HE Ya-peng;CHEN Yi-jing;SHI Xiao;ZHANG Bao-li;WEN Zhan-hua;CHEN Chun-shan;LI Bo;DU Ying-chun;Beijing Aquatic Wildlife Rescue and Conservation Center;Zhengzhou Fengyang Foreign Language School;
关键词：
infectious hematopoietic necrosis virus;;trout;;loop-mediated isothermal amplification;;N gene
摘  要：
A reverse transcription loop-mediated isothermal amplification method for detection of trout infectious haematopoietic necrosis virus(IHNV) in both of laboratory and field was established in this study. A set of specific primers were designed based on the IHNV N gene sequence. IHNV RNA was used as a template for RT-LAMP in a reaction mixture containing reverse transcriptase and Bst DNA polymerase. Positive samples exhibited a fluorescent green color whereas negative samples exhibited a reddish brown color. The optimum temperature for the reaction was 64 ℃. Specific tests results showed that this method was capable to detect the IHNV had no cross action with SVCV, HRV, VHSV and H_2O. Sensitivity test results showed that this method could detect 1.0×10~(-4) μg/μL IHNV RNA. In summary, the method established in this study was suitable for field detection of IHNV and convenient perform quarantine of mass samples with high specificity and sensitivity, rapidity, simple, low cost, and without relying on any special equipment.

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