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Development of a recombinase polymerase amplification (RPA) fluorescence assay for the detection of enterocytozoon hepatopenaei (EHP)

机译:用于检测肠细胞肝肝癌(EHP)的重组酶聚合酶扩增(RPA)荧光测定的研制

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摘要

The emerging microsporidian parasite Enterocytozoon hepatopenaei (EHP) causes retardation of shrimp growth, leading to signi?cant ?nancial losses in shrimp aquaculture. Therefore, the development of an efficient and sensitive detection method will be conducive to the prevention and control of the shrimp parasite. In this study, we developed and evaluated a rapid real-time recombinase polymerase amplification (RPA) method that can detect EHP within 15 min at a constant temperature of 38.5 °C. The detection limit of this EHP RPA was 10 copies/μL of DNA molecules per reaction. The specificity of EHP RPA was tested, and the assay did not cross-react with white spot syndrome virus (WSSV), shrimp hemocyte iridescent virus (SHIV), infectious hypodermal and hematopoietic necrosis virus (IHHNV), or Vibrio parahaemolyticus . Field and clinical applicability of this assay was evaluated using 61 field samples. The coincidence rate of the detection results for the clinical samples between RPA and qPCR was 95.1 %. In summary, the real-time RPA analysis provides an efficient and sensitive detection method for EHP.
机译:新兴磨床寄生虫肠细胞肠肝肝缺血(EHP)引起虾生长的延迟,导致Signi?虾水产养殖中的遗失损失。因此,高效敏感的检测方法的发展将有利于预防和控制虾寄生虫。在该研究中,我们开发并评估了快速实时重组酶聚合酶扩增(RPA)方法,其可以在38.5℃的恒定温度下在15分钟内检测EHP。该EHP RPA的检测限为每次反应10拷贝/μLDNA分子。测试了EHP RPA的特异性,测定与白斑综合征病毒(WSSV),虾血细胞虹吸病病毒(SHIV),传染性皮下和造血坏死病毒(IHHNV)或血管溶血性溶血性的影响没有交叉反应。使用61个田间样品评估该测定的场和临床适用性。 RPA和QPCR之间的临床样品的检测结果的重合率为95.1%。总之,实时RPA分析为EHP提供了一种有效敏感的检测方法。

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