Title of article :
Comparison of Two Multiplex PCR Systems for Meat Species Authentication
Author/Authors :
Al-taghlubee, D Department of Food Hygiene - Faculty of Veterinary Medicine - University of Tehran, Tehran, Iran , Misaghi, A Department of Food Hygiene - Faculty of Veterinary Medicine - University of Tehran, Tehran, Iran , Shayan, P Department of Environment - Tehran North Branch, Islamic Azad University, Tehran, Iran , Akhondzadeh Basti, A Department of Food Hygiene - Faculty of Veterinary Medicine - University of Tehran, Tehran, Iran , Gandomi, H Department of Food Hygiene - Faculty of Veterinary Medicine - University of Tehran, Tehran, Iran , Shayan, D Research Institute Molecular Biological System Transfer (MBST), Tehran, Iran
Abstract :
Background: Meat species adulteration has become a problem of concern. This study
aimed to compare two previously published multiplex Polymerase Chain Reaction (PCR)
methods for meat species authentication.
Methods: The primers used in the first multiplex PCR involved species-specific reverse
primer for sheep, goat, cattle, pig, and donkey with universal forward primer. In the
second multiplex PCR, the primers included species-specific forward and reverse primer
for pork, lamb, ostrich, horse, and cow. The extracted DNA was then amplified with
species-specific primers and with mix primers separately in the respective multiplex PCR.
Results: The first multiplex PCR was accompanied with cross reactivity, whereas the second
multiplex PCR was specific as expected for pork, lamb, ostrich, horse, and cow. The
first set of multiplex PCR showed not always amplification of all species-specific DNAs
with a mixture of DNA from mentioned animals. Regarding the second set of primers, the
extracted DNA of different meat species was amplified with corresponding species
primers as simplex PCR resulting in specific amplicons for species DNA prepared from
sheep, ostrich, horse, pig, and cattle with the specific PCR products of 119, 155, 253, 100,
and 311 bp, respectively.
Conclusion: Based on the present investigation, we recommend the multiplex PCR with
the second set of primers included species-specific forward and reverse primers for
species authentication of five meat types, including pork, lamb, ostrich, horse, as well as
cow.
Keywords :
Fraud , Meat , DNA , Multiplex Polymerase Chain- Reaction , Food Analysis
Journal title :
Astroparticle Physics