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Species-Specific Detection and Quantification of Toxic Marine Dinoflagellates Alexandrium tamarense and A. catenella byReal-Time PCR Assay

机译:实时荧光定量PCR检测有毒海洋鞭毛藻亚历山大藻和链孢菌的物种特异性检测和定量

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摘要

A Real-time polymerase chain reaction (PCR) assay was designed and evaluated for rapid detection and quantification of the toxic dinoflagellates Alexandrium catenella and A. tamarense, which cause paralytic shellfish poisoning. Two sets of PCR primers and fluorogenic probes targeting these two species were derived from the sequence of 28S ribosomal DNA. PCR specificity was examined in closely related Alexandrium spp. and many other microalgae. A. catenella-specific primers and probe detected the PCR amplification only from A. catenella strains, and nonspecific signals were not detected from any microalgae. Also, A. tamarense-specific primers and probe also detected the targeted species, suggesting the strict species specificity of each PCR. This assay could detect one cell of each species, showing its high sensitivity. Moreover, using the developed standard curves, A. tamarense and A. catenella could be quantified in agreement with the quantification by optical microscopy. The performance characteristics of species specificity, sensitivity, and rapidity suggest that this method is applicable to the monitoring of the toxic A. tamarense and A. catenella.
机译:设计并评估了实时聚合酶链反应(PCR)分析法,用于快速检测和定量引起有麻痹性贝类中毒的有毒鞭毛藻亚历山大藻和塔氏杆菌。从28S核糖体DNA序列中获得了针对这两个物种的两组PCR引物和荧光探针。在密切相关的亚历山大菌种中检查PCR的特异性。和许多其他微藻。链霉菌特异性引物和探针仅从链霉菌菌株中检​​测到PCR扩增,从任何微藻类中均未检测到非特异性信号。此外,Amar tamarense特异的引物和探针也检测到了目标物种,这表明每种PCR都具有严格的物种特异性。该测定法可以检测每个物种的一个细胞,显示出其高灵敏度。而且,使用开发的标准曲线,可以与光学显微镜的定量结果一致地对番茄和番茄进行定量。物种特异性,灵敏性和快速性的性能特征表明,该方法可用于监测有毒的番茄,番茄和链霉菌。

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