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对虾白斑综合症病毒变性高效液相色谱检测方法的建立与应用
引用本文:赵巍,马亚,赵玉然,杨大伟,梁成珠,刘荭,何俊强,史秀杰,岳志芹.对虾白斑综合症病毒变性高效液相色谱检测方法的建立与应用[J].中国动物检疫,2011,28(5):47-50.
作者姓名:赵巍  马亚  赵玉然  杨大伟  梁成珠  刘荭  何俊强  史秀杰  岳志芹
作者单位:1. 中国海洋大学,山东青岛,266003;山东出入境检验检疫局技术中心,山东青岛,266002
2. 山东出入境检验检疫局技术中心,山东青岛,266002
3. 中国海洋大学,山东青岛,266003;安徽农业大学,安徽合肥,230036
4. 深圳出入境检验检疫局水生动物疫病国家重点实验室,广东深圳,518010
基金项目:国家质量监督检验检疫总局科研项目
摘    要:据对虾白斑综合症病毒(WSSV)的基因保守序列,使用Primer Explorer V3软件设计了2条引物,利用PCR的扩增产物,结合变性高效液相色谱(DHPLC)技术,建立了一种对虾白斑综合症病毒的DHPLC快速检测方法。该检测方法特异性好,与传染性皮下和造血器官坏死病毒、斑节对虾杆状病毒、肝胰腺细小病毒、对虾杆状病毒以及对虾基因组DNA无交叉反应;检测灵敏度较高,约为10-5ng/μL,高于常规PCR及荧光定量PCR的灵敏度。用建立的DHPLC方法对100尾对虾样品进行了临床检测,结果与荧光定量PCR检测结果一致。WSSV的DHPLC检测方法,特异性强、灵敏度高,是对WSSV进行有效检测的一种新方法。

关 键 词:变性高效液相色谱  对虾  白斑综合症病毒  检测

Establishment and Application of Denaturing High-performance Liquid Chromatography for White Spot Syndrome Virus
Zhao Wei,Ma Y,Zhao Yuran,Yang Dawei,Liang Chengzhu,Liu Hong,He Junqiang,Shi Xiujie,Yue Zhiqin.Establishment and Application of Denaturing High-performance Liquid Chromatography for White Spot Syndrome Virus[J].China Journal Of Animal Quarantine,2011,28(5):47-50.
Authors:Zhao Wei  Ma Y  Zhao Yuran  Yang Dawei  Liang Chengzhu  Liu Hong  He Junqiang  Shi Xiujie  Yue Zhiqin
Institution:1.Ocean University of China,Qingdao 266003,China;2.Shandong Technical Center of Shandong Entry-Exit Inspection and Quarantine Bureau,Qingdao 266002,China;3.The Key Lab of Aquatic Animal Diseases,Shenzhen Entry-Exit Inspection and Quarantine Bureau,Shenzhen 518010,China;4.Anhui Agricultulal University,Hefei 230036,China)
Abstract:Two specific primers were designed based on conservative gene of white spot syndrome virus(WSSV) using Primer Explorer V3 software.A detection method for WSSV using the denaturing high-performance liquid chromatography(DHPLC) was established.The WSSV LAMP assay did not react with infetious hypodermal and haematopoietic necrosis virus(IHHNV),monodon baculovirus(MBV),hepatopancreatic parvovirus(HPV),baculovirus penaei(BP) or genome DNA of shrimp,indicating the good specificity.The detection limit of DHPLC assay was approximately 10-5 ng/μL WSSV DNA,which was higher than that of conventional PCR and the real-time PCR.100 clinical shrimp samples were detected with the DHPLC method and the results were consistent with the real-time PCR method.The DHPLC assay was accurate,specific and sensitive,having great potential in diagnosis of WSSV infection.
Keywords:DHPLC  shrimp  WSSV  detection
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