4.7 Article

Development of fast and sensitive real-time qPCR assay based on a novel probe for detection of porcine DNA in food sample

Journal

LWT-FOOD SCIENCE AND TECHNOLOGY
Volume 84, Issue -, Pages 686-692

Publisher

ELSEVIER
DOI: 10.1016/j.lwt.2017.06.043

Keywords

Real-time PCR; Porcine DNA detection; ZENTm probe; Processed food; Meat adulteration

Funding

  1. Brunei Research Council of Negara Brunei Darussalam [BRC-10]

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Porcine adulteration of food is objectionable to a sizeable percentage of the global population owing to health concerns and/or religious faiths. However, unintentional or intentional porcine adulteration is common in the food industry - for which a strong demand prevails for a fast and sensitive method to detect and quantify porcine DNA in foods. In this study, we are reporting the development of a real-time qPCR assay based on the novel ZEN (TM) probe for the fast and sensitive detection of porcine DNA in real food samples. The assay's specificity to porcine DNA was confirmed against nine species. Standard curve was developed and sensitivity of the assay was tested with six ten-fold dilutions of the DNA standard. Our novel assay successfully detected as low as 1 pg/mu l of porcine DNA and as low as 0.001% pork in the raw pork-chicken binary mixture. (C) 2017 Elsevier Ltd. All rights reserved.

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