P. Praipue, S. Klinbunga and P. Jarayabhand
Published June 15, 2010
Genet. Mol. Res. 9 (2): 1136-1152 (2010)
DOI 10.4238/vol9-2gmr808

About the authors
P. Praipue, S. Klinbunga and P. Jarayabhand

Corresponding author
S. Klinbunga
E-mail: sirawut@biotec.or.th

ABSTRACT

Amplified fragment length polymorphism (AFLP) analysis was carried out on representative individuals of wild Haliotis asinina using 64 primer combinations. Nine polymorphic AFLPs were cloned and sequenced. Sequence-specific primers were designed from six AFLP-derived fragments. Three sequence-characterized amplified region (SCAR) markers (HaSCAR320, HaSCAR295, HaSCAR327) were selected for genotyping of 8-month-old domesticated stocks of H. asinina cultured separately at Sichang Marine Science Research andTraining Station (N = 95) and at a hatchery in Trang province (N = 40) using single-strand conformational polymorphism analysis. Genotypes of wild abalone originating from Talibong Island (N = 25), Cambodia (N = 22), and the P0 progeny established from Samet Island founders (N = 20) were also investigated. Significant genetic differentiation (P < 0.0001 for the exact test and FST = 0.8759-0.8919, P < 0.001) between abalone from the Gulf of Thailand (Cambodia and Samet Island – east) and the Andaman Sea (Talibong Island – west) were observed. This demonstrated the strong biogeographic structure of H. asinina in Thai waters. Non-overlapping composite genotypes for wild abalone from different coastal regions allow us to determine founder contributions in domesticated abalone stocks. Almost all Sichang Marine Science Research and Training Station and the Trang province hatchery stocks exhibited the east coast genotypes (97% of the 135 samples). We suggest that abalone from the east coast population have better survival rates under cultivated conditions than those from the west coast population.

Key words: AFLP; SSCP; Abalone; Genetic diversity; Domestication; Stock identification