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Real-time PCR Detection of Dinophysis Species in Irish Coastal Waters

机译:实时荧光定量PCR检测爱尔兰沿海水域中的物种

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Diarrhetic shellfish toxin-producing Dinophysis species occur in Irish coastal waters throughout the year. Dinophysis acuta and Dinophysis acuminata are the most commonly occurring species and are responsible for the majority of closures of Irish mussel farms. This study describes the development of a qualitative real-time polymerase chain reaction (PCR) assay for identification of D. acuta and D. acuminata in Irish coastal waters. DNA sequence information for the D1-D2 region of the large ribosomal sub-unit (LSU) was obtained, following single-cell PCR of D. acuta and D. acuminata cells isolated from Irish coastal locations. PCR primers and hybridization probes, specific for the detection of D. acuta, were designed for real-time PCR on the LightCyclerO. The LightCyclerO software melt curve analysis programme determined that D. acuta was identified by a melt-peak at 61pC, while D. acuminata cells produced a melt peak at 48pC. The limit of detection of the real-time PCR assay was determined to be one to ten plasmid copies of the LSU D1-D2 target region for both species and one to five D. acuminata cells. Lugol's preserved water samples were also tested with the assay. The real-time PCR assay identified Dinophysis species in 100% of samples found to contain Dinophysis species by light microscopy and had a greater than 90% correlation with light microscopy for identification of D. acuta and D. acuminata in the samples. The assay can identify and discriminate D. acuta and D. acuminata at low numbers in Irish waters and has the potential to add value to the Irish phytoplankton monitoring programme.
机译:全年在爱尔兰沿海水域中产生产生腹泻性贝类毒素的恐龙。 Dinophysis acuta和Dinophysis acuminata是最常见的物种,是造成爱尔兰贻贝养殖场关闭的主要原因。这项研究描述了定性实时聚合酶链反应(PCR)分析方法的发展,该方法可用于鉴定爱尔兰沿海水域的D. acuta和D. acuminata。在对从爱尔兰沿海地区分离出的A. acuta和D. acuminata细胞进行单细胞PCR之后,获得了大核糖体亚基(LSU)D1-D2区的DNA序列信息。专为检测金刀鱼而设计的PCR引物和杂交探针可用于LightCyclerO上的实时PCR。 LightCyclerO软件的熔解曲线分析程序确定了通过61pC的熔解峰鉴定出了D. acuta,而D. acuminata细胞在48pC产生了熔解峰。实时荧光定量PCR检测的检测限被确定为LSU D1-D2靶标区域的两种质粒和1到5种尖锐梭菌细胞的1到10个质粒拷贝。卢戈尔保存的水样品也用该测定法进行了测试。实时PCR分析通过光学显微镜鉴定出100%的样品中含有恐龙物种,并与光学显微镜具有90%以上的相关性以鉴定样品中的D. acuta和D. acuminata。该测定法可以识别和区分在爱尔兰水域中数量很少的锐角杜鹃和尖锐梭菌,并有可能为爱尔兰的浮游植物监测计划增值。

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