Sweijd, Neville A., Bowie, Rauri C.K., Lopata, Andreas L., Marinaki, Anthony M., Harley, Eric H., and Cook, Peter A. (1998) A PCR technique for forensic species level identification of abalone tissue. Journal of Shellfish Research, 17 (3). pp. 889-895.

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Abstract

Athough the incidence of abalone poaching is increasing in South Africa, several alleged poachers have been acquitted in cases where the state has been unable to prove that the confiscated meat is of the local abalone. Halimis midae. This species is illegally exported to the Far East by poaching syndicates, a practice that is undermining the legitimate industry. To solve this, a polymerase chain reaction (PCR) technique that targets a portion of the lysin gene of several abalone species and unequivocally distinguishes between H. midae and H. spadicea (a sympatric congeneric) has been developed. The PCR primers specifically amplify approximately 1 ,300 bp of genomic DNA from dried, cooked, and fresh abalone tissue. A smaller fragment of 1 46 bp is used for canned abalone. Restriction fragment length polymorphism (RFLP) exploit interspecific polymorphisms that discriminate between these two species. The method can also be used to identify H. rubra and can easily be adapted to other abalone species under the same threat of overexploitation.

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