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环介导等温扩增(LAMP)检测坚果中产毒和产志贺毒素大肠埃希氏菌的方法的建立。

Development of Loop-Mediated Isothermal Amplification (LAMP) Assays for the Rapid Detection of Toxigenic and in Nuts.

机构信息

Department of Agricultural Sciences, Food, Natural Resources and Engineering, University of Foggia, Via Napoli, 25-71122 Foggia, Italy.

National Research Council-Institute of Molecular Biology and Pathology, P.le A. Moro, 5-00185 Rome, Italy.

出版信息

Int J Mol Sci. 2024 Mar 29;25(7):3809. doi: 10.3390/ijms25073809.

Abstract

species create major postharvest problems due to the food losses caused by their mere presence and the hazardous mycotoxins they produce, such as aflatoxin B1 (AFB1) and ochratoxin A (OTA). These mycotoxins are mainly produced by and , respectively. In this study, we developed a rapid detection method for the two aforementioned species based on loop-mediated isothermal amplification (LAMP). The primers were designed to target genes belonging to the mycotoxin clusters and for and , respectively. Result visualization was carried out in real time via the detection of fluorescent signals. The method developed showed high sensitivity and specificity, with detection limits of 0.3 and 0.03 pg/reaction of purified DNA of and , respectively. The assays were further implemented on inoculated nuts, including pistachios and almonds, after one-step crude DNA extraction. These tests revealed a detection level of 0.5 spore/g that shows the effectiveness of LAMP as a rapid method for detecting potentially toxigenic spp. directly in food. The validation of the assays included tests on a larger scale that further confirmed their sensitivity and specificity, as well as enabling the production of ready-to-use LAMP prototype kits. These kits are easy to use and aim to simplify the screening of food samples in order to monitor the presence of specific contaminations.

摘要

种属会造成重大的采后问题,不仅因为它们的存在会导致食物损耗,还因为它们会产生有害的真菌毒素,如黄曲霉毒素 B1(AFB1)和赭曲霉毒素 A(OTA)。这些真菌毒素主要由 和 产生。在本研究中,我们基于环介导等温扩增(LAMP)开发了一种用于快速检测上述两种种属的方法。引物设计针对与真菌毒素簇 和 相关的基因,分别用于 和 。通过检测荧光信号,实时可视化结果。所开发的方法具有高灵敏度和特异性,对 和 的纯化 DNA 的检测限分别为 0.3 和 0.03 pg/反应。进一步在经过一步粗提 DNA 处理的接种坚果(包括开心果和杏仁)上进行了检测。这些测试显示,在食品中直接检测潜在产毒 的孢子的检测水平为 0.5 孢子/g,表明 LAMP 作为一种快速检测方法的有效性。检测方法的验证包括更大规模的测试,进一步证实了它们的灵敏度和特异性,并能够生产即用型 LAMP 原型试剂盒。这些试剂盒易于使用,旨在简化食品样本的筛选,以监测特定 污染的存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c16a/11011790/534e090f67bb/ijms-25-03809-g001.jpg

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