AI Article Synopsis

  • Pufferfish are important to the economy as edible fish, but misidentification can result in poisoning, making accurate species identification vital.
  • This study utilized the mtDNA COI gene to create specific primers that can quickly identify six of the 21 pufferfish species sold in Korea via a multiplex PCR method.
  • The method proved effective, allowing for the identification of each species within six hours, thus helping to prevent mislabeled fish, protect consumers, and reduce poisoning risks.

Article Abstract

Pufferfish ( spp.) are economically important edible marine fish. Mistakes in pufferfish classification can lead to poisoning; therefore, accurate species identification is critical. In this study, we used the mtDNA cytochrome c oxidase subunit I gene (COI) to design specific primers for six species among the 21 domestic or imported pufferfish species legally sold for consumption in Korea. We rapidly and simultaneously identified these pufferfish species using a highly efficient, multiplex polymerase chain reaction (PCR) system with the six species-specific primers. The results showed that species-specific multiplex PCR (multiplex species-specific polymerase chain reaction; MSS-PCR) either specifically amplified PCR products of a unique size or failed. MSS-PCR yielded amplification fragment lengths of 897 bp for , 822 bp for , 667 bp for , 454 bp for , 366 bp for , and 230 bp for using the species-specific primers and a control primer (ca. 1,200 bp). We visualized the results using agarose gel electrophoresis to obtain accurate contrasts of the six species. MSS-PCR analysis is easily performed and provides identification results within 6 h. This technique is a powerful tool for the discrimination of species and will help prevent falsified labeling, protect consumer rights, and reduce the risk of pufferfish poisoning..

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6985294PMC
http://dx.doi.org/10.12717/DR.2019.23.4.367DOI Listing

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