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杨会勇, 那广水, 朱术会, 邹秉杰, 奚涛, 周国华. 利用线性指数PCR-焦磷酸测序技术快速检测3种海洋弧菌[J]. 中国药科大学学报, 2009, 40(5): 460-464.
引用本文: 杨会勇, 那广水, 朱术会, 邹秉杰, 奚涛, 周国华. 利用线性指数PCR-焦磷酸测序技术快速检测3种海洋弧菌[J]. 中国药科大学学报, 2009, 40(5): 460-464.
YANG Hui-yong, NA Guang-shui, ZHU Shu-hui, ZOU Bing-jie, XI Tao, ZHOU Guo-hua. Rapid discrimination of three species of marine Vibrios by using linear-after-the-exponential PCR coupled with pyrosequencing[J]. Journal of China Pharmaceutical University, 2009, 40(5): 460-464.
Citation: YANG Hui-yong, NA Guang-shui, ZHU Shu-hui, ZOU Bing-jie, XI Tao, ZHOU Guo-hua. Rapid discrimination of three species of marine Vibrios by using linear-after-the-exponential PCR coupled with pyrosequencing[J]. Journal of China Pharmaceutical University, 2009, 40(5): 460-464.

利用线性指数PCR-焦磷酸测序技术快速检测3种海洋弧菌

Rapid discrimination of three species of marine Vibrios by using linear-after-the-exponential PCR coupled with pyrosequencing

  • 摘要: 目的 : 建立一种基于线性指数聚合酶链式反应(linear-after-the-exponential PCR,LATE-PCR)焦磷酸测序技术快速检测致病性海洋弧菌的方法。 方法 : 首先根据海洋弧菌的16S rRNA基因和外膜蛋白K(OmpK)基因的目的片段设计引物并优化反应条件进行LATE-PCR扩增,其次利用酶促反应处理PCR产物中干扰焦磷酸测序反应的副产物,最后加入退火引物后直接进行焦磷酸测序。 结果 : 成功进行了LATE-PCR扩增,制备出足量单链DNA模板供焦磷酸测序反应;取1~2 μL的PCR产物即可获得理想的焦磷酸测序信号。测序结果与Sanger法的结果一致,测得序列与GenBank所报道的相符合。通过对16S rRNA基因片段的检测,可以确认样品是否为海洋弧菌;通过对OmpK基因目的片段的检测可以初步区分弧菌种类,对3种常见弧菌:副溶血弧菌、哈维弧菌和溶藻弧菌成功地进行了检测。 结论 : 本方法结果准确,灵敏度高,操作简便且成本低,可快速检测大量样品,在弧菌快速检测和诊断中具有很好的应用前景。

     

    Abstract: Aim :To develop a method based on linear-after-the-exponential-polymerase chain reaction(LATE-PCR) coupled with pyrosequencing for rapid detection of pathogenic marine Vibrios. Methods :Firstly,LATE-PCR used to detect the target fragments on 16S rRNA gene and outer membrane protein K(OmpK) gene of Vibrios was achieved by carefully designing primers and optimizing reaction conditions.Secondly,the by-products of LATE-PCR were eliminated by a series of enzymatic reactions to reduce interference to pyrosequencing.Finally,the samples were detected directly by pyrosequencing after annealing. Results :The ideal single chain and enough amount can be obtained for pyrosequencing by 1-2 μL PCR product,and the results were consistent with those of Sanger method.The sequences of the Vibrio samples by pyrosequencing were consistent with GenBank report,and the Vibrio samples can be confirmed through the detection of the target fragment on 16S rRNA gene;and the species of Vibrios can be distinguished by the detection of the target fragment on OmpK gene.We successfully discriminated three Vibrios i. e. Vibrio parahaemolyticusV.harveyi and V.alginolyticus. Conclusion :Our method has high sensitivity,simple operation and low cost. It is also suitable for detecting a mass of samples.It is promising that this assay is used in the diagnosis and control of the infection caused by Vibrios and correlative research.

     

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