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Development of novel isothermal-based DNA amplification assay for detection of pig tissues in adulterated meat
For the first time, we describe an innovative polymerase spiral reaction (PSR) assay for the rapid, simple, and accurate detection of pig tissues or pork in adulterated meat including heat-treated and processed ones. The PSR assay specifically targeting the mitochondrial cytochrome b (cyt-b) gene of...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079161/ https://www.ncbi.nlm.nih.gov/pubmed/37362349 http://dx.doi.org/10.1007/s00217-023-04250-9 |
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author | Danawadkar, Vinaykumar N. Ruban, S. Wilfred Milton, Arockiasamy Arun Prince Kiran, M. Momin, Kasanchi M. Ghatak, Sandeep Mohan, H. V. Porteen, Kannan |
author_facet | Danawadkar, Vinaykumar N. Ruban, S. Wilfred Milton, Arockiasamy Arun Prince Kiran, M. Momin, Kasanchi M. Ghatak, Sandeep Mohan, H. V. Porteen, Kannan |
author_sort | Danawadkar, Vinaykumar N. |
collection | PubMed |
description | For the first time, we describe an innovative polymerase spiral reaction (PSR) assay for the rapid, simple, and accurate detection of pig tissues or pork in adulterated meat including heat-treated and processed ones. The PSR assay specifically targeting the mitochondrial cytochrome b (cyt-b) gene of the pig was successfully optimized permitting assay results in 65 min time. The developed detection method was 100% specific amplifying only the cyt-b gene and displaying negative results with all the tested non-pork meats. The sensitivity of the developed PSR (760 fg porcine DNA) was tenfold better than the end-point PCR and able to detect heat-treated (121 °C) and adulterated (0.5% pork in beef) meat and processed pork products such as sausages, salami, meatball, soup, curry, etc. The developed PSR-based method can be used for point-of-care detection with minimum instrumentation and technical expertise to guarantee instant clearance of exported and imported meat products. This is the first time that PSR has been adapted for food authenticity purposes. |
format | Online Article Text |
id | pubmed-10079161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-100791612023-04-07 Development of novel isothermal-based DNA amplification assay for detection of pig tissues in adulterated meat Danawadkar, Vinaykumar N. Ruban, S. Wilfred Milton, Arockiasamy Arun Prince Kiran, M. Momin, Kasanchi M. Ghatak, Sandeep Mohan, H. V. Porteen, Kannan Eur Food Res Technol Original Paper For the first time, we describe an innovative polymerase spiral reaction (PSR) assay for the rapid, simple, and accurate detection of pig tissues or pork in adulterated meat including heat-treated and processed ones. The PSR assay specifically targeting the mitochondrial cytochrome b (cyt-b) gene of the pig was successfully optimized permitting assay results in 65 min time. The developed detection method was 100% specific amplifying only the cyt-b gene and displaying negative results with all the tested non-pork meats. The sensitivity of the developed PSR (760 fg porcine DNA) was tenfold better than the end-point PCR and able to detect heat-treated (121 °C) and adulterated (0.5% pork in beef) meat and processed pork products such as sausages, salami, meatball, soup, curry, etc. The developed PSR-based method can be used for point-of-care detection with minimum instrumentation and technical expertise to guarantee instant clearance of exported and imported meat products. This is the first time that PSR has been adapted for food authenticity purposes. Springer Berlin Heidelberg 2023-04-06 /pmc/articles/PMC10079161/ /pubmed/37362349 http://dx.doi.org/10.1007/s00217-023-04250-9 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Paper Danawadkar, Vinaykumar N. Ruban, S. Wilfred Milton, Arockiasamy Arun Prince Kiran, M. Momin, Kasanchi M. Ghatak, Sandeep Mohan, H. V. Porteen, Kannan Development of novel isothermal-based DNA amplification assay for detection of pig tissues in adulterated meat |
title | Development of novel isothermal-based DNA amplification assay for detection of pig tissues in adulterated meat |
title_full | Development of novel isothermal-based DNA amplification assay for detection of pig tissues in adulterated meat |
title_fullStr | Development of novel isothermal-based DNA amplification assay for detection of pig tissues in adulterated meat |
title_full_unstemmed | Development of novel isothermal-based DNA amplification assay for detection of pig tissues in adulterated meat |
title_short | Development of novel isothermal-based DNA amplification assay for detection of pig tissues in adulterated meat |
title_sort | development of novel isothermal-based dna amplification assay for detection of pig tissues in adulterated meat |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079161/ https://www.ncbi.nlm.nih.gov/pubmed/37362349 http://dx.doi.org/10.1007/s00217-023-04250-9 |
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