CAJ | 학술논문

本根据GenBank上公布的布鲁氏菌BCSP31基因保守区域序列设计合成一对特异性引物与TapMan探针，建立整套快速准确鉴定布鲁氏菌的实时定量荧光PCR检测体系。以实验室构建的克隆有布鲁氏菌目的片段的重组质粒为标准品，进行实时定量荧光PCR反应检测，通过优化反应条件，建立标准曲线。以标准品为模板，对该方法的特异性、敏感性与重复性进行检测与分析。并以临床样本进行检测的结果进行比较分析，结果表明，该检测体系的检测灵敏度高，重复性与特异性良好。本研究建立的实时定量荧光PCR可用于准确检测样本中的少量的布鲁氏菌，具有良好的应用前景和市场价值。
본근거GenBank상공포적포로씨균BCSP31기인보수구역서렬설계합성일대특이성인물여TapMan탐침，건립정투쾌속준학감정포로씨균적실시정량형광PCR검측체계。이실험실구건적극륭유포로씨균목적편단적중조질립위표준품，진행실시정량형광PCR반응검측，통과우화반응조건，건립표준곡선。이표준품위모판，대해방법적특이성、민감성여중복성진행검측여분석。병이림상양본진행검측적결과진행비교분석，결과표명，해검측체계적검측령민도고，중복성여특이성량호。본연구건립적실시정량형광PCR가용우준학검측양본중적소량적포로씨균，구유량호적응용전경화시장개치。
According to the conserved sequences of Brucella BCSP31 genes, a pair of specific primers and probe were designed and synthesized to establish a rapid and accurate detection system for identification of Brucella by real-time quantitative PCR assay. The prepared Brucella recombinant plasmid containing target gene fragment was taken as the standard in the real-time quantitative fluorescent PCR, and the standard curve was then established. The specificity, sensitivity and reproducibility of this detection system were determined with standard as template. Comparison of clini-cal samples and standard samples showed that the PCR system was of high sensitivity, reproducibility and specificity. In conclusion, the study established real-time quantitative fluorescent PCR assay which could be used to detect small amount of Brucella in sample, with sound applicable prospect and quite good market value.