基于RPA-CRISPR/Cas12a的沙氏弧菌可视化检测方法的建立

Establishment of RPA-CRISPR/Cas12a-based visual detection of Vibrio chagasii

  • 摘要:
    目的 建立基于RPA-CRISPR/Cas12a的沙氏弧菌实时荧光检测法和试纸条检测法,满足牡蛎新发病原沙氏弧菌的快速检测需求。
    方法 实验针对沙氏弧菌toxR基因设计特异性片段,优选RPA引物和crRNA序列,确保基因标志物的准确扩增与识别;当CRISPR/Cas12a系统识别到RPA扩增的病原靶标基因并激活其反式切割活性后,生物素修饰的单链DNA荧光探针作为报告分子被切割,分别依据蓝光下的荧光强度和试纸条的显色情况判定检测结果;实验采用多种弧菌验证检测方法的特异性,并通过不同浓度沙氏弧菌菌液评估2种检测方法的灵敏度;最终将2种检测方法与PCR方法进行真实样本检测对比。
    结果 本研究成功建立了RPA-CRISPR/Cas12a荧光检测法和试纸检测法,且均表现出优异的特异性,可准确识别沙氏弧菌,整个检测流程可在1 h内完成;2种方法的检测限均达到100 CFU/mL,检测结果与PCR高度一致(符合率100%)。
    结论 本研究开发的基于RPA-CRISPR/Cas12a的荧光检测法和试纸检测法,突破了传统方法的局限,显著缩短检测时间,且无需复杂仪器,操作简便,为沙氏弧菌的现场快速检测提供了可靠的技术支持。本研究为沙氏弧菌的快速检测提供了高效、便捷的新方法,对水产养殖病害防控和食品安全保障具有重要意义。

     

    Abstract: Vibrio chagasii is an emerging pathogen in Crassostrea angulata aquaculture, causing significant economic losses and posing risks to food safety. Traditional detection methods, such as PCR, are time-consuming and rely on complex equipment, making them unsuitable for on-site rapid detection. Therefore, developing fast, sensitive, and simple detection methods is of great importance. To meet the need for rapid detection of V. chagasii, this study integrated recombinase polymerase amplification (RPA) with the CRISPR/Cas12a system, aiming to establish real-time fluorescence detection method and test strip detection based on RPA-CRISPR/Cas12a. Specific fragments targeting the toxR gene of V. chagasii were designed, and RPA primers and crRNA sequences were optimized to ensure accurate gene amplification and identification. Upon recognition of the RPA-amplified target gene, the CRISPR/Cas12a system activated its trans-cleavage activity, cleaving biotin-modified single-stranded DNA fluorescent probes. Detection results were determined by the fluorescence brightness under blue light and the color development of the test strip. The experiment used multiple Vibrio species to verify the specificity of the detection methods and evaluated the sensitivity of the two detection methods through different concentrations of V. chagasii bacterial solution. The two methods were further compared with PCR using real samples. The established RPA-CRISPR/Cas12a-based fluorescence detection method and test strip detection demonstrated excellent specificity, accurately identifying V. chagasii, and the whole detection process could be completed within 1 h. Both methods achieved a detection limit of 100 CFU/mL, showing high consistency with PCR results (100% concordance). The RPA-CRISPR/Cas12a-based detection methods developed in this study are fast, sensitive, and easy to operate, providing a reliable technical solution for the on-site detection of V. chagasii. This study offers two novel, efficient, and convenient methods for the rapid detection of V. chagasii, contributing significantly to disease control in aquaculture and ensuring food safety.

     

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