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Rapid detection of duck ingredient in adulterated foods by isothermal recombinase polymerase amplification assays
Duck is often used in meat fraud as a substitute for more expensive meats. Rapid detection of duck ingredient in meat products is of great significance for combating meat fraud and safeguarding the interests of consumers. Therefore, we aim to develop duck-specific recombinase polymerase amplificatio...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9841362/ https://www.ncbi.nlm.nih.gov/pubmed/36654874 http://dx.doi.org/10.1016/j.fochms.2023.100162 |
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author | Zhou, Cang Wang, Jinfeng Xiang, Jialin Fu, Qi Sun, Xiaoxia Liu, Libing Ai, Lianfeng Wang, Jianchang |
author_facet | Zhou, Cang Wang, Jinfeng Xiang, Jialin Fu, Qi Sun, Xiaoxia Liu, Libing Ai, Lianfeng Wang, Jianchang |
author_sort | Zhou, Cang |
collection | PubMed |
description | Duck is often used in meat fraud as a substitute for more expensive meats. Rapid detection of duck ingredient in meat products is of great significance for combating meat fraud and safeguarding the interests of consumers. Therefore, we aim to develop duck-specific recombinase polymerase amplification (RPA)-based assays for the rapid detection of duck ingredient in animal-derived foods. Using Cytb gene as target, the real-time RPA and RPA combined with lateral flow strips (LFS RPA) were developed successfully for the rapid detection of ducks in 20 min at 39 °C and 40 °C, respectively. The assays did not show cross-reactions with 6 other livestock and poultry. The developed RPA assays could detect 10 pg duck genomic DNA per reaction and 0.1 % (w/w) duck ingredient in duck and mutton mixed powder within 30 min, including a rapid nucleic acid extraction. Furthermore, duck ingredient could be detected in 30 different actual foods including heat-processed meats and blood products. Therefore, duck-specific real-time RPA and LFS RPA assays were successfully developed with good specificity and sensitivity, which could enable rapid detection of duck ingredient in the field and provide technical support for combating the meat fraud. |
format | Online Article Text |
id | pubmed-9841362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-98413622023-01-17 Rapid detection of duck ingredient in adulterated foods by isothermal recombinase polymerase amplification assays Zhou, Cang Wang, Jinfeng Xiang, Jialin Fu, Qi Sun, Xiaoxia Liu, Libing Ai, Lianfeng Wang, Jianchang Food Chem (Oxf) Research Article Duck is often used in meat fraud as a substitute for more expensive meats. Rapid detection of duck ingredient in meat products is of great significance for combating meat fraud and safeguarding the interests of consumers. Therefore, we aim to develop duck-specific recombinase polymerase amplification (RPA)-based assays for the rapid detection of duck ingredient in animal-derived foods. Using Cytb gene as target, the real-time RPA and RPA combined with lateral flow strips (LFS RPA) were developed successfully for the rapid detection of ducks in 20 min at 39 °C and 40 °C, respectively. The assays did not show cross-reactions with 6 other livestock and poultry. The developed RPA assays could detect 10 pg duck genomic DNA per reaction and 0.1 % (w/w) duck ingredient in duck and mutton mixed powder within 30 min, including a rapid nucleic acid extraction. Furthermore, duck ingredient could be detected in 30 different actual foods including heat-processed meats and blood products. Therefore, duck-specific real-time RPA and LFS RPA assays were successfully developed with good specificity and sensitivity, which could enable rapid detection of duck ingredient in the field and provide technical support for combating the meat fraud. Elsevier 2023-01-09 /pmc/articles/PMC9841362/ /pubmed/36654874 http://dx.doi.org/10.1016/j.fochms.2023.100162 Text en © 2023 The Authors. Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Zhou, Cang Wang, Jinfeng Xiang, Jialin Fu, Qi Sun, Xiaoxia Liu, Libing Ai, Lianfeng Wang, Jianchang Rapid detection of duck ingredient in adulterated foods by isothermal recombinase polymerase amplification assays |
title | Rapid detection of duck ingredient in adulterated foods by isothermal recombinase polymerase amplification assays |
title_full | Rapid detection of duck ingredient in adulterated foods by isothermal recombinase polymerase amplification assays |
title_fullStr | Rapid detection of duck ingredient in adulterated foods by isothermal recombinase polymerase amplification assays |
title_full_unstemmed | Rapid detection of duck ingredient in adulterated foods by isothermal recombinase polymerase amplification assays |
title_short | Rapid detection of duck ingredient in adulterated foods by isothermal recombinase polymerase amplification assays |
title_sort | rapid detection of duck ingredient in adulterated foods by isothermal recombinase polymerase amplification assays |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9841362/ https://www.ncbi.nlm.nih.gov/pubmed/36654874 http://dx.doi.org/10.1016/j.fochms.2023.100162 |
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