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วารสารเทคโนโลยีชีวภาพการผลิตปศุสัตว์



                                                      Introduction

                     Species identification of animal product using molecular technology is currently an important

              issue for food authenticity since incorrect labeling of origin may have negative consequences such

              as food allergy, religion aspect, and illegal mixed cheaper meat to the products, etc. (Ghovvati et
              al., 2009). Species detection is also involved in wildlife management in order to define the animal

              species  (Li-Chin  Tsai  et  al.,  2007)  which  endangered  species  are  illegally  killed.  Both  food

              authentication and protection of biodiversity require reliable and accurate methods for determining.

              Moreover, species identification is one of significant steps in the genetic traceability system of food

              process (Hobbs, 2004; Smith et al., 2005; Schwagele, 2005). Recently, many studies focused on

              the development of DNA based technology to differentiate the species of the animals (Bottero et al.,

              2003;  Dalmasso  et  al.,  2004)  including  the  advantage  of  Polymerase  Chain  Reaction  (PCR)

              technology. PCR method can be used to amplify small amount of specific DNA target sequences in

              a short period of time faster than other methods such as polypeptide identification or protein analysis
              including electrophoretic, immunological, mass-spectrometric and chromatographic techniques since

              the protein will degrade rapidly after animal died or being cooked. (Gouli et al., 1999). Among of

              selected genes, Cytochrome b (cyt b) gene, one of the most mitochondrial (mt) genes which differs

              five- to tenfold of DNA copies higher than nuclear genes, is used for identifying animal species. This

              gene is found in all vertebrates and does not undergo recombination, enables closely related species

              to be differentiated and identified (Matsuda et al., 2005). Kocher et al. (1989) reported universal

              primers  which  could  be  used  to  amplify  a  wide  range  of  vertebrate  species.  Although  these
              researches had been done on several kinds of animals, there was no report of animal species

              identification using multiplex PCR technique that included the 6 animal species which were targeted

              in this study.

                     The purpose of this study is to develop a molecular method, based on cyt b gene, multiplex

              PCR technique to identify the 6 species of animals (cattle, buffalo, goat, sheep, chicken and pig) as

              mainly food source in Thailand.










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