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多物种产品中的海鲜鉴定:评估16SrRNA、细胞色素b和细胞色素氧化酶亚基I通用引物的效率作为建立元条形码下一代测序技术的初步分析步骤

Seafood Identification in Multispecies Products: Assessment of 16SrRNA, cytb, and COI Universal Primers' Efficiency as a Preliminary Analytical Step for Setting up Metabarcoding Next-Generation Sequencing Techniques.

作者信息

Giusti Alice, Tinacci Lara, Sotelo Carmen G, Marchetti Martina, Guidi Alessandra, Zheng Wenjie, Armani Andrea

机构信息

FishLab, Department of Veterinary Sciences, University of Pisa , Via delle Piagge 2, 56124 Pisa, Italy.

Instituto de Investigaciones Marinas (IIM-CSIC) , Eduardo Cabello 6, 36208 Vigo, Spain.

出版信息

J Agric Food Chem. 2017 Apr 5;65(13):2902-2912. doi: 10.1021/acs.jafc.6b05802. Epub 2017 Mar 23.

Abstract

Few studies applying NGS have been conducted in the food inspection field, particularly on multispecies seafood products. A preliminary study screening the performance and the potential application in NGS analysis of 14 "universal primers" amplifying 16SrRNA, cytb, and COI genes in fish and cephalopods was performed. Species used in surimi preparation were chosen as target. An in silico analysis was conducted to test primers' coverage capacity by assessing mismatches (number and position) with the target sequences. The 9 pairs showing the best coverage capacity were tested in PCR on DNA samples of 53 collected species to assess their amplification performance (amplification rate and amplicon concentration). The results confirm that primers designed for the 16SrRNA gene amplification are the most suitable for NGS analysis also for identification of multispecies seafood products. In particular, the primer pair of Chapela et al. (2002) is the best candidate.

摘要

在食品检测领域,尤其是在多物种海产品方面,应用新一代测序技术(NGS)的研究较少。我们开展了一项初步研究,筛选了14种用于扩增鱼类和头足类动物16SrRNA、细胞色素b(cytb)和细胞色素氧化酶亚基I(COI)基因的“通用引物”在NGS分析中的性能及潜在应用。用于制作鱼糜的物种被选为目标物种。通过评估与目标序列的错配情况(数量和位置)进行了计算机模拟分析,以测试引物的覆盖能力。对覆盖能力最佳的9对引物在53种采集物种的DNA样本上进行了PCR测试,以评估它们的扩增性能(扩增率和扩增子浓度)。结果证实,设计用于扩增16SrRNA基因的引物最适合用于NGS分析,也适用于多物种海产品的鉴定。特别是,Chapela等人(2002年)的引物对是最佳候选引物。

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