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使用新型超快PCR系统快速现场检测虾过敏原原肌球蛋白

Rapid on-site detection of shrimp allergen tropomyosin using a novel ultrafast PCR system.

作者信息

Kim Mi-Ju, Kim Hee-In, Kim Jae-Hwan, Suh Seung-Man, Kim Hae-Yeong

机构信息

Institute of Life Sciences and Resources, Department of Food Science and Biotechnology, Kyung Hee University, 1732 Deogyeong-daero, Giheung-gu, Yongin, 17104 Republic of Korea.

出版信息

Food Sci Biotechnol. 2018 Sep 27;28(2):591-597. doi: 10.1007/s10068-018-0479-x. eCollection 2019 Apr.

DOI:10.1007/s10068-018-0479-x
PMID:30956872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6431315/
Abstract

Shrimp is seafood that can commonly trigger allergic reactions. In this study, the ultrafast real-time PCR assay with portable device was developed to detect a shrimp-derived major allergen, tropomyosin, without complicated DNA extraction. For shrimp allergen detection, a specific primer pair was designed based on the shrimp tropomyosin gene and 18S ribosomal RNA gene as internal control. Primer specificity was assessed using 8 common seafood species. Serially diluted shrimp DNA was used to determine the limit of detection of the ultrafast PCR system, which was approximately 3.2 pg. Twenty-three food samples containing shrimp were evaluated to verify the applicability of a direct ultrafast PCR method for detecting shrimp allergens without DNA isolation. It took less than 30 min from sample preparation-to-result analysis to detect shrimp DNA in raw and processed samples. Therefore, this PCR system can be effectively and conveniently utilized in the field to detect shrimp in various food products.

摘要

虾是一种常见的可引发过敏反应的海鲜。在本研究中,开发了一种配备便携式设备的超快速实时PCR检测方法,用于检测虾源主要过敏原原肌球蛋白,无需复杂的DNA提取过程。为了检测虾过敏原,基于虾原肌球蛋白基因设计了一对特异性引物,并以18S核糖体RNA基因作为内对照。使用8种常见海鲜物种评估引物特异性。采用系列稀释的虾DNA来确定超快速PCR系统的检测限,约为3.2 pg。对23份含虾的食品样本进行评估,以验证直接超快速PCR方法在不进行DNA分离的情况下检测虾过敏原的适用性。从样品制备到结果分析,检测生的和加工后的样本中的虾DNA耗时不到30分钟。因此,该PCR系统可在现场有效且便捷地用于检测各类食品中的虾。