Recombinase polymerase amplification assays for the identification of pork and horsemeat

•Pork and horse DNA can be detected in eleven minutes.•The assays are based on the technique recombinase polymerase amplification.•The whole procedure can be implemented by a mobile suitcase laboratory.•The control of origin of species in meat products can be simplified. Detection of animal species...

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Veröffentlicht in:Food chemistry 2020-08, Vol.322, p.126759-126759, Article 126759
Hauptverfasser: Kissenkötter, Jonas, Böhlken-Fascher, Susanne, Forrest, Matthew S., Piepenburg, Olaf, Czerny, Claus-Peter, Abd El Wahed, Ahmed
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Sprache:eng
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Zusammenfassung:•Pork and horse DNA can be detected in eleven minutes.•The assays are based on the technique recombinase polymerase amplification.•The whole procedure can be implemented by a mobile suitcase laboratory.•The control of origin of species in meat products can be simplified. Detection of animal species in meat product is crucial to prevent adulterated and unnecessary contamination during processing. Gold standard is the real-time PCR assays, which can be conducted at highly equipped laboratories. Toward the development of point-of-need test, two rapid molecular assays based on recombinase polymerase amplification (RPA) for the detection of pork and horse DNA were established. Target genes are the porcine mitochondrial ND2 and equine ATP 6–8 genes. The pork and horse_RPA assays detected 16 and one DNA molecules/µl in eleven to six minutes, respectively. The myoglobin in the meat did not influence the assays performances, while the presence of high background-DNA induced a one log decrease in the sensitivity. Both assays are highly specific and identify down to 0.1% of their target DNA in meat mixtures. Both RPA assays could be used on-site as a rapid and mobile detection system to determine contamination of meat products.
ISSN:0308-8146
1873-7072
DOI:10.1016/j.foodchem.2020.126759