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Identification of Selected Tuna Species in Commercial Products
This study was conducted to develop systems for the identification of four tuna species (skipjack tuna Katsuwonus pelamis, yellowfin tuna Thunnus albacares, bullet tuna Auxis sp. and Atlantic bonito Sarda sp). At first, raw samples of these species and a mix intended as internal control were prepare...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924337/ https://www.ncbi.nlm.nih.gov/pubmed/33672711 http://dx.doi.org/10.3390/molecules26041137 |
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author | Servusova, Eliska Piskata, Zora |
author_facet | Servusova, Eliska Piskata, Zora |
author_sort | Servusova, Eliska |
collection | PubMed |
description | This study was conducted to develop systems for the identification of four tuna species (skipjack tuna Katsuwonus pelamis, yellowfin tuna Thunnus albacares, bullet tuna Auxis sp. and Atlantic bonito Sarda sp). At first, raw samples of these species and a mix intended as internal control were prepared for the authentication of fish muscle tissue of the genus Thunnus sp., Auxis sp. and Sarda sp. DNA from raw muscle tissue, the mix and samples was extracted with the DNeasy mericon Food Kit (Qiagen GmbH, Hilden, Germany). The concentration and purity of DNA in raw samples were evaluated using a spectrophotometer. Primers and probe sequences were specifically designed to identify the selected species. In addition, primers and a probe for the endogenous 12S rRNA gene were designed to determine the presence of amplifiable fish (especially tuna) DNA in samples. Furthermore, the species specificity of the designed primers and probes was verified in DNA samples of various tuna and bonito species. Limit of detection for the selected species was calculated as well as the coefficient of determination R(2) and efficiency of real-time PCR testing was determined. To evaluate the developed real-time PCR methods, 70 commercial tuna products were analysed. The results show that mislabelling of fish products can still be encountered and, moreover, the presence of an additional species can be identified. |
format | Online Article Text |
id | pubmed-7924337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79243372021-03-03 Identification of Selected Tuna Species in Commercial Products Servusova, Eliska Piskata, Zora Molecules Article This study was conducted to develop systems for the identification of four tuna species (skipjack tuna Katsuwonus pelamis, yellowfin tuna Thunnus albacares, bullet tuna Auxis sp. and Atlantic bonito Sarda sp). At first, raw samples of these species and a mix intended as internal control were prepared for the authentication of fish muscle tissue of the genus Thunnus sp., Auxis sp. and Sarda sp. DNA from raw muscle tissue, the mix and samples was extracted with the DNeasy mericon Food Kit (Qiagen GmbH, Hilden, Germany). The concentration and purity of DNA in raw samples were evaluated using a spectrophotometer. Primers and probe sequences were specifically designed to identify the selected species. In addition, primers and a probe for the endogenous 12S rRNA gene were designed to determine the presence of amplifiable fish (especially tuna) DNA in samples. Furthermore, the species specificity of the designed primers and probes was verified in DNA samples of various tuna and bonito species. Limit of detection for the selected species was calculated as well as the coefficient of determination R(2) and efficiency of real-time PCR testing was determined. To evaluate the developed real-time PCR methods, 70 commercial tuna products were analysed. The results show that mislabelling of fish products can still be encountered and, moreover, the presence of an additional species can be identified. MDPI 2021-02-20 /pmc/articles/PMC7924337/ /pubmed/33672711 http://dx.doi.org/10.3390/molecules26041137 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Servusova, Eliska Piskata, Zora Identification of Selected Tuna Species in Commercial Products |
title | Identification of Selected Tuna Species in Commercial Products |
title_full | Identification of Selected Tuna Species in Commercial Products |
title_fullStr | Identification of Selected Tuna Species in Commercial Products |
title_full_unstemmed | Identification of Selected Tuna Species in Commercial Products |
title_short | Identification of Selected Tuna Species in Commercial Products |
title_sort | identification of selected tuna species in commercial products |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924337/ https://www.ncbi.nlm.nih.gov/pubmed/33672711 http://dx.doi.org/10.3390/molecules26041137 |
work_keys_str_mv | AT servusovaeliska identificationofselectedtunaspeciesincommercialproducts AT piskatazora identificationofselectedtunaspeciesincommercialproducts |