Development of loop-mediated isothermal amplification (LAMP) assay for rapid and direct screening of yellowfin tuna (Thunnus albacares) in commercial fish products

被引:12
作者
Ali, Ashraf [1 ]
Kreitlow, Antonia [2 ]
Ploetz, Madeleine [2 ]
Normanno, Giovanni [1 ]
Abdulmawjood, Amir [2 ]
机构
[1] Univ Foggia, Dept Agr Sci Food Nat Resources & Engn DAFNE, Foggia, Italy
[2] Univ Vet Med Hannover, Inst Food Qual & Food Safety, Hannover, Germany
关键词
SPECIES IDENTIFICATION; FRESH; DNA; AUTHENTICATION; SAMPLES; OBESUS; COD;
D O I
10.1371/journal.pone.0275452
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tuna is one of the most widely consumed fish on the European market, being available in various consumable options. Among them, Thunnus albacares, also called yellowfin tuna, is a delicacy and is consumed by millions of people around the world. Due to its comparatively high cost and demand, it is more vulnerable to fraud, where low-cost tuna or other fish varieties might be replaced for economic gain. In this study, a loop-mediated isothermal amplification (LAMP) assay was developed and validated for targeting the mitochondrial cytochrome b gene for fast and direct detection of Thunnus albacares, which is a valuable tuna species. The analytical specificity was confirmed using 18 target samples (Thunnus albacares) and 18 samples of non-target fish species. The analytical sensitivity of the LAMP assay was 540 fg DNA per reaction. In addition, a simple and direct swab method without time-consuming nucleic acid extraction procedures and the necessity for cost-intensive laboratory equipment was performed that allowed LAMP detection of Thunnus albacares samples within 13 minutes. Due to its high specificity and sensitivity, the LAMP assay can be used as a rapid and on-site screening method for identifying Thunnus albacares, potentially providing a valuable monitoring tool for food authenticity control by the authorities.
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页数:13
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