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dc.contributor.authorRichardson, Marina A.
dc.contributor.authorNenadic, Nikolina
dc.contributor.authorWingfield, Max
dc.contributor.authorMcDougall, Carmel
dc.date.accessioned2024-05-28T10:30:05Z
dc.date.available2024-05-28T10:30:05Z
dc.date.issued2024-05-21
dc.identifier302273898
dc.identifier2f46f72d-2e3d-4e7e-b735-a65d48471fbe
dc.identifier85193937462
dc.identifier.citationRichardson , M A , Nenadic , N , Wingfield , M & McDougall , C 2024 , ' The development of multiplex PCR assays for the rapid identification of multiple Saccostrea species, and their practical applications in restoration and aquaculture ' , BMC Ecology and Evolution , vol. 24 , no. 67 . https://doi.org/10.1186/s12862-024-02250-1en
dc.identifier.issn2730-7182
dc.identifier.urihttps://hdl.handle.net/10023/29941
dc.descriptionThe Nature Conservancy 2020 Reef-Builder program.en
dc.description.abstractBackground The ecology and biology of oysters (Ostreidae) across the tropics is poorly understood. Morphological plasticity and shared characteristics among oysters have resulted in the misidentification of species, creating challenges for understanding basic species-specific biological information that is required for restoration and aquaculture. Genetic barcoding has proven essential for accurate species identification and understanding species geographic ranges. To reduce the costs of molecular species identification we developed multiplex assays using the cytochrome c oxidase subunit I (COI or cox1) barcoding gene for the rapid identification of five species of oysters within the genus Saccostrea that are commonly found in Queensland, Australia: Saccostrea glomerata, Saccostrea lineage B, Saccostrea lineage F, Saccostrea lineage G, and Saccostrea spathulata (lineage J). Results Multiplex assays were successful in species-specific amplification of targeted species. The practical application of these primers was tested on wild spat collected from a pilot restoration project in Moreton Bay, Queensland, with identified species (S. glomerata, lineage B and lineage G) validated by Sanger sequencing. DNA sampling by extraction of oyster pallial fluid was also tested on adult oysters collected from the Noosa estuary in Queensland to assess whether oysters were able to be identified non-destructively. DNA concentrations as low as 1 ng/ μL still amplified in most cases, allowing for identification, and mortality at 6 weeks post pallial fluid collection was low (3 out of 104 sampled oysters). Conclusion These multiplex assays will be essential tools for species identification in future studies, and we successfully demonstrate their practical application in both restoration and aquaculture contexts in Queensland. The multiplex assays developed in this study outline easily replicable methods for the development of additional species-specific primer sets for the rapid identification of other species of Saccostrea found across the Indo-Pacific, which will be instrumental in unravelling the taxonomic ambiguities within this genus in tropical regions.
dc.format.extent3024100
dc.language.isoeng
dc.relation.ispartofBMC Ecology and Evolutionen
dc.subjectDASen
dc.titleThe development of multiplex PCR assays for the rapid identification of multiple Saccostrea species, and their practical applications in restoration and aquacultureen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.contributor.institutionUniversity of St Andrews. Scottish Oceans Instituteen
dc.identifier.doi10.1186/s12862-024-02250-1
dc.description.statusPeer revieweden


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