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Quantitative PCR Coupled with Melt Curve Analysis for Detection of Selected Pseudo-nitzschia spp. (Bacillariophyceae) from the Northwestern Mediterranean Sea

机译:定量PCR与熔解曲线分析相结合用于检测选定的拟南芥属。 (Bacillariophyceae)来自西北地中海

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摘要

The frequency and intensity of Pseudo-nitzschia spp. blooms along the coast of Catalonia have been increasing over the past 20 years. As species from this genus that are documented as toxigenic have been found in local waters, with both toxic and nontoxic species cooccurring in the same bloom, there is a need to develop management tools for discriminating the difference. Currently, differentiation of toxic and nontoxic species requires time-consuming electron microscopy to distinguish taxonomic features that would allow identification as to species, and cryptic species can still remain misidentified. In this study, cells of Pseudo-nitzschia from clonal cultures isolated from seawater were characterized to their species identity using scanning electron microscopy, and subsamples of each culture were used to create an internal transcribed spacer 1 (ITS-1), 5.8S, and ITS-2 ribosomal DNA database for development of species-specific quantitative PCR (qPCR) assays. Once developed, these qPCR assays were applied to field samples collected over a 2-year period in Alfaques Bay in the northwestern Mediterranean Sea to evaluate the possibility of a comprehensive surveillance for all Pseudo-nitzschia spp. using molecular methods to supplement optical microscopy, which can discern taxonomy only to the genus level within this taxon. Total Pseudo-nitzschia cell density was determined by optical microscopy from water samples collected weekly and compared to results obtained from the sum of eight Pseudo-nitzschia species-specific qPCR assays using duplicate samples. Species-specific qPCR followed by melt curve analysis allowed differentiation of amplicons and identification of false positives, and results correlated well with the total Pseudo-nitzschia cell counts from optical microscopy.
机译:拟南芥属的频率和强度。在过去的20年中,加泰罗尼亚沿海的花朵不断增加。由于已在当地水域发现了该种被证明具有毒性的物种,有毒和无毒物种同时出现在同一水华,因此需要开发一种管理工具来区分这种差异。当前,对有毒和无毒物种的区分需要耗时的电子显微镜来区分分类学特征,以允许对物种进行鉴定,而隐秘物种仍可能会被误认。在这项研究中,使用扫描电子显微镜对从海水中分离的克隆培养物中的假性奈瑟菌的细胞进行了特征鉴定,并使用每种培养物的亚样品创建了内部转录间隔子1(ITS-1),5.8S和ITS-2核糖体DNA数据库,用于开发物种特异性定量PCR(qPCR)分析。一旦开发完成,这些qPCR测定法将应用于在地中海西北部的阿尔法克斯湾(Alfaques Bay)历时2年收集的野外样品,以评估对所有拟南芥属物种进行全面监视的可能性。使用分子方法补充光学显微镜,这只能将分类法识别到该分类中的属水平。通过光学显微镜从每周收集的水样中确定总假性紫薇细胞密度,并将其与使用重复样品的八种假性紫薇物种特异性qPCR分析的总和相比较。物种特异性qPCR,然后进行熔解曲线分析,可以区分扩增子并鉴定假阳性,结果与光学显微镜下的假性尼兹菌总细胞计数高度相关。

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