文章摘要
荣小军,廖梅杰,张 正,王印庚,刘智超,李 彬,王 岚,陈贵平.迟缓爱德华氏菌SYBR Green I实时荧光定量PCR检测方法的建立及其应用[J].水产学报,2013,37(12):1829~1838
迟缓爱德华氏菌SYBR Green I实时荧光定量PCR检测方法的建立及其应用
Development of an SYBR Green I real-time PCR assay for detection of Edwardsiella tarda and its application
投稿时间:2013-07-03  修订日期:2013-09-20
DOI:DOI:10.3724/SP.J.1231.2014.48798
中文关键词: 迟缓爱德华氏菌  gyrB基因  实时定量PCR  SYBR Green I
英文关键词: gyrB gene  Edwardsiella tarda  real-time PCR  SYBR Green I
基金项目:国家“八六三”高技术研究发展计划(2012AA10A412-4);科研院所技术开发研究专项项目(2011EG34219);国家科技支撑计划(2012BAD17B03);国家自然科学基金项目(30901120,31202016);天津市农业科技成果转化与推广项目(201104080)
作者单位
荣小军 中国海洋大学海洋生命学院 
廖梅杰 中国水产科学研究院黄海水产研究所,农业部海洋渔业可持续发展重点实验室 
张 正 中国水产科学研究院黄海水产研究所,农业部海洋渔业可持续发展重点实验室 
王印庚 中国水产科学研究院黄海水产研究所,农业部海洋渔业可持续发展重点实验室 
刘智超 中国海洋大学海洋生命学院 
李 彬 中国水产科学研究院黄海水产研究所,农业部海洋渔业可持续发展重点实验室 
王 岚 中国水产科学研究院黄海水产研究所,农业部海洋渔业可持续发展重点实验室 
陈贵平 中国水产科学研究院黄海水产研究所,农业部海洋渔业可持续发展重点实验室 
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中文摘要:
      根据克隆得到的迟缓爱德华氏菌gyrB基因序列设计并合成一对特异性引物,通用性和特异性检测结果显示所设计的引物具有良好的种间特异性和种内通用性,构建含gyrB基因的重组质粒作为标准品,经过反应体系优化后建立了检测迟缓爱德华氏菌的SYBR Green I实时荧光定量PCR检测方法。结果显示,该方法线性关系良好,在Tm为63 ℃时,扩增产物的熔解曲线仅有一个单特异峰,扩增所得标准曲线为y=-3.32x+39.38,相关系数为0.998,扩增效率为1.00,最低能检测到60个拷贝。应用建立的方法对人工感染的大菱鲆病样进行了检测,3个被检样品均呈阳性反应,证明该方法具有较好的适用性。研究表明,所建立的实时荧光定量PCR方法具有特异、敏感、快速、定量的优点,可用于迟缓爱德华氏菌病的快速检测。
英文摘要:
      According to the sequenced gyrB gene sequence of Edwardsiella tarda,a pair of primers was designed for establishing an SYBR Green I real-time fluorescence quantitative PCR method.A 207 bp gene fragment was amplified from chromosomal DNA of E.tarda from different sources,and no positive reaction was detected in 9 other bacteria species using conventional PCR,which indicated that the primer pair has good inter-species specificity and intra-species commonality.Recombinant plasmid containing gyrB gene of E.tarda was constructed and used to construct the standard curve.The standard curves was y=-3.32x+39.38,the correlation coefficient was 0.998 and the amplification efficiency was 1.00,which indicated that it had a good linear relationship between initial templates and Ct values.The melting curve has only one specific peak when annealing temperature was 63 ℃.The detection limit of the assay was 60 copies per reaction.Turbot samples infected by E.tarda artificially were detected using the real-time PCR assay.All the three samples were positive,which had good agreement with bacteriological analysis by isolation and culture.The results showed that the developed SYBR Green I real-time PCR assay had the advantages of specificity,sensitivity,rapidity and quantification,and would be helpful for E.tarda diagnosis and epidemiology investigation.
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