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Molecular identification of the economically important freshwater mussels ( M ollusca– B ivalvia– U nionoida) of T hailand: developing species‐specific markers from AFLP s
Author(s) -
Vannarattanarat S.,
Zieritz A.,
Kanchanaketu T.,
Kovitvadhi U.,
Kovitvadhi S.,
Hongtrakul V.
Publication year - 2014
Publication title -
animal genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 81
eISSN - 1365-2052
pISSN - 0268-9146
DOI - 10.1111/age.12115
Subject(s) - biology , amplified fragment length polymorphism , primer (cosmetics) , specific identification , mussel , molecular marker , zoology , polymerase chain reaction , ecology , genetics , genetic diversity , gene , population , chemistry , demography , organic chemistry , sociology
Summary Shells of certain freshwater mussel (Unionoida) species are highly demanded and serve as raw material for a range of decorative and pharmaceutical products. In Thailand, most animals for this purpose are currently harvested from wild populations, with unionoid culture still being in its infancy. Whilst reliable species identification is a prerequisite for developing a large‐scale industry, identification by morphological means is hampered by extensive phenotypic plasticity and poor knowledge of species delimitations. To facilitate alternative molecular identification, we developed species‐specific markers for the three Thai unionoids with considerable economic potential ( CEP ): that is, Chamberlainia hainesiana , Hyriopsis desowitzi and Hyriopsis myersiana . For this purpose, amplified fragment length polymorphism ( AFLP ) fingerprints using 24 specific primer pairs were generated for eight samples of each CEP species and four samples of the closely related, non‐ CEP species Contradens contradens . Cloning and sequencing of 13 CEP species‐specific AFLP bands revealed fragment collision at three occasions. In total, 16 species‐specific primer pairs were designed and tested on 92 Thai specimens spanning seven species and four genera. Thereby, specificity of (1) three primers to C. hainesiana , (2) one primer to H. desowitzi + Hyriopsis bialata , (3) one primer to H. myersiana + H. bialata and (4) four primers to all three Hyriopsis species tested was confirmed. Respective multiplex PCR protocols are provided. The developed primers enable cheap, quick and reliable identification of the Thai CEP species by one to three PCR s and offer a tool for a range of additional applications within mussel culture and ecological and evolutionary research on these important organisms.