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用于快速检测扁牡蛎中[具体物质1]和[具体物质2]的环介导等温扩增技术。

Loop-Mediated Isothermal Amplification for the Fast Detection of and in Flat Oysters.

作者信息

Cano Irene, Wood Gareth, Stone David, Noyer Mathilde, Canier Lydie, Arzul Isabelle

机构信息

The International Centre of Excellence for Aquatic Animal Health, Cefas Weymouth Laboratory, Weymouth, Dorset DT4 8UB, UK.

The Institut Français de Recherche pour l'Exploitation de la Mer Ifremer, RBE-SG2M-ASIM, Station de La Tremblade, Avenue de Mus de Loup, La Tremblade, 17390 Brest, France.

出版信息

Pathogens. 2024 Jan 30;13(2):132. doi: 10.3390/pathogens13020132.

Abstract

The haplosporidian parasites (BO) and (BE) are serious oyster pathogens. Two independent laboratories evaluated fluorescence real-time loop-mediated isothermal amplification (LAMP) assays for rapidly detecting these parasites. Specific LAMP assays were designed on the BO and BE genes. A further generic assay was conceived on a conserved region of the gene to detect both species. The optimal reaction temperature varied from 65 to 67 °C depending on the test and instrument. Melting temperatures were 89.8-90.2 °C, 87.0-87.6 °C, and 86.2-86.6 °C for each of the BO, BE, and generic assays. The analytical sensitivity of these assays was 50 copies/µL in a 30 min run. The BO and BE test sensitivity was ~1 log lower than a real-time PCR, while the generic test sensitivity was similar to the real-time PCR. Both the BO and BE assays were shown to be specific; however, the generic assay potentially cross-reacts with . The performance of the LAMP assays evaluated on samples of known status detected positives within 7-20 min with a test accuracy of 100% for the BO and generic tests and a 95.8% accuracy for BE. The ease of use, rapidity and affordability of these tests allow for field deployment.

摘要

单孢子虫寄生虫(BO)和(BE)是牡蛎的严重病原体。两个独立实验室评估了用于快速检测这些寄生虫的荧光实时环介导等温扩增(LAMP)检测方法。针对BO和BE基因设计了特异性LAMP检测方法。基于该基因的保守区域构思了一种通用检测方法,以检测这两种物种。最佳反应温度根据检测和仪器的不同在65至67°C之间变化。BO、BE和通用检测方法的熔解温度分别为89.8 - 90.2°C、87.0 - 87.6°C和86.2 - 86.6°C。这些检测方法在30分钟的运行中分析灵敏度为50拷贝/微升。BO和BE检测的灵敏度比实时PCR低约1个对数,而通用检测的灵敏度与实时PCR相似。BO和BE检测方法均显示具有特异性;然而,通用检测方法可能与[未提及的物种]发生交叉反应。在已知状态的样本上评估的LAMP检测方法的性能在7 - 20分钟内检测到阳性,BO和通用检测的检测准确率为100%,BE的准确率为95.8%。这些检测方法的易用性、快速性和可承受性使其能够在现场部署。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e91a/10893247/16fff296de76/pathogens-13-00132-g001.jpg

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