| Summary: | For the in situ and sensitive detection of benthic dinoflagellates, we have established an integrated loop-mediated isothermal amplification (LAMP) assay based on <i>Ostreopsis</i> cf. <i>ovata</i> and <i>Amphidinium massartii</i>. To detect the two species, a set of species-specific primers was constructed between the ITS gene and D1–D6 LSU gene, and the reaction temperature, time, and buffer composition were optimized to establish this method. In addition, the specificity of the LAMP primers was verified both in strains established in the laboratory and in field samples collected from the Jeju coastal waters, Korea. With the LAMP assay, the analysing time was within 45 to 60 min, which may be shorter than that with the conventional PCR. The detection sensitivity of the LAMP assay for <i>O</i>. cf. <i>ovata</i> or <i>A. massartii</i> was comparable to other molecular assays (PCR and quantitative PCR (qPCR)) and microscopy examination. The detection limit of LAMP was 0.1 cell of <i>O</i>. cf. <i>ovata</i> and 1 cell of <i>A. massartii</i>. The optimized LAMP assay was successfully applied to detect <i>O.</i> cf. <i>ovata</i> and <i>A. massartii</i> in field samples. Thus, this study provides an effective method for detecting target benthic dinoflagellate species, and could be further implemented to monitor phytoplankton in field surveys as an altenative.
|
|---|
