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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.
Afiliação
  • Danawadkar VN; Department of Livestock Products Technology, Veterinary College, Karnataka Veterinary, Animal and Fisheries Sciences University, Hebbal, Bangalore, India.
  • Ruban SW; Department of Livestock Products Technology, Veterinary College, Karnataka Veterinary, Animal and Fisheries Sciences University, Hebbal, Bangalore, India.
  • Milton AAP; Division of Animal and Fisheries Sciences, ICAR Research Complex for NEH Region, Umiam, Meghalaya India.
  • Kiran M; Department of Livestock Products Technology, Veterinary College, Karnataka Veterinary, Animal and Fisheries Sciences University, Nandinagar, Bidar, India.
  • Momin KM; Division of Animal and Fisheries Sciences, ICAR Research Complex for NEH Region, Umiam, Meghalaya India.
  • Ghatak S; Division of Animal and Fisheries Sciences, ICAR Research Complex for NEH Region, Umiam, Meghalaya India.
  • Mohan HV; Department of Veterinary Public Health, Hebbal Veterinary College, Karnataka Veterinary, Animal and Fisheries Sciences University, Hebbal, Bangalore, India.
  • Porteen K; Department of Veterinary Public Health, Madras Veterinary College, Tamil Nadu Veterinary and Animal Sciences University, Chennai, India.
Eur Food Res Technol ; : 1-9, 2023 Apr 06.
Article em En | MEDLINE | ID: mdl-37362349
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Eur Food Res Technol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Eur Food Res Technol Ano de publicação: 2023 Tipo de documento: Article