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Development of Species-Specific PCR Primers for the Rapid and Simultaneous Identification of the Six Species of Genus .

作者信息

Dong Chun Mae, Park Yeon Jung, Noh Jae Koo, Noh Eun Soo, An Cheul Min, Kang Jung-Ha, Park Jung Youn, Kim Eun-Mi

机构信息

Biotechnology Research Division, National Institute of Fisheries Science, Busan 46083, Korea.

出版信息

Dev Reprod. 2019 Dec;23(4):367-375. doi: 10.12717/DR.2019.23.4.367. Epub 2019 Dec 31.

DOI:10.12717/DR.2019.23.4.367
PMID:31993542
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6985294/
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..

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98fc/6985294/5b8cbfbe531e/dr-23-4-367-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98fc/6985294/8efd9d7b99c1/dr-23-4-367-g1a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98fc/6985294/b51af8964aaa/dr-23-4-367-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98fc/6985294/5b8cbfbe531e/dr-23-4-367-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98fc/6985294/8efd9d7b99c1/dr-23-4-367-g1a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98fc/6985294/b51af8964aaa/dr-23-4-367-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98fc/6985294/5b8cbfbe531e/dr-23-4-367-g3.jpg

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本文引用的文献

1
DNA-Based Methods for the Identification of Commercial Fish and Seafood Species.基于DNA的商业鱼类和海鲜物种鉴定方法
Compr Rev Food Sci Food Saf. 2008 Jun;7(3):280-295. doi: 10.1111/j.1541-4337.2008.00046.x.
2
TaqMan qPCR for detection and quantification of mitochondrial DNA from toxic pufferfish species.用于检测和定量有毒河豚物种线粒体DNA的TaqMan实时荧光定量PCR技术
Toxicon. 2015 Aug;102:43-7. doi: 10.1016/j.toxicon.2015.05.016. Epub 2015 May 27.
3
Molecular identification of pufferfish species using PCR amplification and restriction analysis of a segment of the 16S rRNA gene.
利用聚合酶链反应(PCR)扩增和 16S rRNA 基因片段的限制性分析对河豚鱼进行分子鉴定。
Comp Biochem Physiol Part D Genomics Proteomics. 2006 Mar;1(1):139-44. doi: 10.1016/j.cbd.2005.09.004. Epub 2005 Nov 9.
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Public health response to puffer fish (Tetrodotoxin) poisoning from mislabeled product.针对因产品标签错误导致的河豚(河豚毒素)中毒事件的公共卫生应对措施。
J Food Prot. 2009 Apr;72(4):810-7. doi: 10.4315/0362-028x-72.4.810.
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Molecular phylogenetic relationships of puffer fish inferred from partial sequences of cytochrome b gene and restriction fragment length polymorphism analysis.基于细胞色素b基因部分序列和限制性片段长度多态性分析推断的河豚分子系统发育关系。
J Agric Food Chem. 2004 Jun 30;52(13):4159-65. doi: 10.1021/jf035462l.
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Identification of the species origin of highly processed meat products by mitochondrial DNA sequences.
PCR Methods Appl. 1995 Feb;4(4):241-3. doi: 10.1101/gr.4.4.241.