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实时荧光定量PCR扩增特异性vapA基因检测杀鲑气单胞菌
引用本文:刘帅,王荻,卢彤岩,曹永生,杨晨,朱国建,李绍戊.实时荧光定量PCR扩增特异性vapA基因检测杀鲑气单胞菌[J].水产学报,2017,41(12):1928-1935.
作者姓名:刘帅  王荻  卢彤岩  曹永生  杨晨  朱国建  李绍戊
作者单位:1. 中国水产科学研究院黑龙江水产研究所,黑龙江 哈尔滨 150070;上海海洋大学水产与生命学院,上海 201306;2. 中国水产科学研究院黑龙江水产研究所,黑龙江 哈尔滨,150070;3. 新疆额尔齐斯河流域开发工程建设管理局,新疆 乌鲁木齐,830000
基金项目:中央级公益性科研院所基本科研业务费专项(HSY201503);新疆维吾尔自治区区域协同创新专项(2016E02052)
摘    要:为实现杀鲑气单胞菌早期快速准确定量检测,研究旨在建立杀鲑气单胞菌的SYBR Green Ⅰ实时荧光定量PCR(Real-time PCR)检测方法。根据GenBank中杀鲑气单胞菌毒力阵列蛋白基因(vapA)保守序列设计并合成一对特异性引物,对其特异性、灵敏度、可重复性和应用性进行评价。结果显示,研究设计的引物具有良好的种间特异性,仅对杀鲑气单胞菌及其亚种有阳性扩增,与其他细菌不发生交叉反应。构建的Real-time PCR标准曲线质粒拷贝数与循环阈值呈良好的线性关系,扩增所得标准曲线分别为y=–4.8345x+42.535,相关系数R~2为0.998,最低检测限为34拷贝/μL,较常规PCR的灵敏度高出约1000倍。应用建立的方法检测人工感染的虹鳟病样,15个被检样品呈阳性反应,与细菌常规鉴定方法结果一致。研究表明,所建立的基于实时荧光定量PCR技术的杀鲑气单胞菌检测方法快速、特异、灵敏,可用于临床诊断和疫病监测。

关 键 词:虹鳟  杀鲑气单胞菌  vapA基因  实时荧光定量PCR
收稿时间:2016/11/9 0:00:00
修稿时间:2017/2/25 0:00:00

Real-time PCR detection of Aeromonas salmonicida by amplification of specific vapA gene
LIU Shuai,WANG Di,LU Tongyan,CAO Yongsheng,YANG Chen,ZHU Guojian and LI Shaowu.Real-time PCR detection of Aeromonas salmonicida by amplification of specific vapA gene[J].Journal of Fisheries of China,2017,41(12):1928-1935.
Authors:LIU Shuai  WANG Di  LU Tongyan  CAO Yongsheng  YANG Chen  ZHU Guojian and LI Shaowu
Institution:Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin 150070, China;College of Fishery and Life Science, Shanghai Ocean University, Shanghai 201306, China,Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin 150070, China,Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin 150070, China,Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin 150070, China,Xinjiang Erqis River Basin Development Construction Management Bureau, Urumqi 830000, China,Xinjiang Erqis River Basin Development Construction Management Bureau, Urumqi 830000, China and Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin 150070, China
Abstract:In order to implement the early and quick quantitative determination of Aeromonas salmonicida, a SYBR Green I Real-time PCR method of A. salmonicida was established based on the pathogen sequence information. Based on the vapA of virulence array protein gene sequence of A. salmonicida, a pair of primers was designed and used in a real time quantitative polymerase chain reaction (qPCR) assay. The specificity, sensitivity, repeatability and application of the system were also evaluated. The results showed that A. salmonicida and its subspecies can be clearly discriminated from the other 10 bacteria species by SYBR Green I Real-time qPCR, which indicated that the primer pair has good inter-species specificity. The standard curve established by recombinant plasmid showed a fine linear relationship between initial templates and threshold cycle, which can be described as y=–4.8345x+42.535 (R2=0.998). The sensitivity analysis showed that the detection limit was 34 copies/μL, which suggested that the sensitivity of Real-time qPCR was about 1000 times higher than that of the conventional PCR assay. The established method was applied to detect the samples in rainbow trout after artificial infection. Results showed that 15 of those samples were positive, which had complete agreement (100%) with bacteriological analysis by isolation and culture. In conclusion, the developed Real-time PCR assay for A. salmonicida is fast, highly specific, and sensitive. This method had a broad application for clinical diagnosis and disease surveillance in aquaculture.
Keywords:Oncorhynchus mykiss  Aeromonas salmonicida  vapA gene  Real-time qPCR
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