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

被引:0
作者
Mi-Ju Kim
Hee-In Kim
Jae-Hwan Kim
Seung-Man Suh
Hae-Yeong Kim
机构
[1] Kyung Hee University,Institute of Life Sciences and Resources, Department of Food Science and Biotechnology
来源
Food Science and Biotechnology | 2019年 / 28卷
关键词
Shrimp; Tropomyosin; Allergen; On-site detection; Ultrafast PCR; Food products;
D O I
暂无
中图分类号
学科分类号
摘要
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.
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页码:591 / 597
页数:6
相关论文
共 137 条
[1]  
Aboud M(2013)Rapid direct PCR for forensic genotyping in under 25 min Electrophoresis. 34 1539-1547
[2]  
Oh HH(2014)Multiplex PCR in species authentication: probability and prospects—a review Food Anal. Method. 7 1933-1949
[3]  
McCord B(2013)Clinical value of component-resolved diagnostics in peanut-allergic patients Allergy. 68 190-194
[4]  
Ali ME(2016)Development of an on-site rapid real-time polymerase chain reaction system and the characterization of suitable DNA polymerases for TaqMan probe technology Anal. Bioanal. Chem. 408 5641-5649
[5]  
Razzak MA(2017)On-site identification of meat species in processed foods by a rapid real-time polymerase chain reaction system Meat Sci. 131 56-59
[6]  
Hamid SBA(2012)Fast real-time PCR for the detection of crustacean allergen in foods J. Agric. Food Chem. 60 1893-1897
[7]  
Eller E(2014)Development of an in-house fast real-time PCR method for detection of fish allergen in foods and comparison with a commercial kit Food Chem. 151 415-420
[8]  
Jensen BC(2016)Ultrafast, sensitive and large-volume on-chip real-time PCR for the molecular diagnosis of bacterial and viral infections Lab Chip. 16 1401-1411
[9]  
Furutani S(2017)Multiplex PCR for identification of Shigellae and Shigella species using novel genetic markers screened using comparative genomics Foodborne Pathog. Dis. 14 400-406
[10]  
Naruishi N(2017)Species identification of commercial jerky products in food and feed using direct pentaplex PCR assay Food Control. 78 1-6