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Development of a real-time PCR method (Taqman) for rapid identification and quantification of Prorocentrum donghaiense |
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| Authors: | Jian Yuan Tiezhu Mi Yu Zhen Zhigang Yu |
| Institution: | 1. College of Marine Life Sciences, Ocean University of China, Qingdao, 266003, P. R. China 4. Key Laboratory of Marine Environment and Ecology, Ministry of Education, Ocean University of China, Qingdao, 266100, P. R. China 5. Key Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, Ocean University of China, Qingdao, 266100, P. R. China 2. College of Environmental Science and Engineering, Ocean University of China, Qingdao, 266100, P. R. China 3. College of Chemistry and Chemical Engineering, Ocean University of China, Qingdao, 266100, P. R. China |
| Abstract: | Prorocentrum donghaiense is a dinoflagellate that is widely distributed in the East China Sea and has become increasingly involved in Harmful Algal Blooms (HABs). Therefore, it is necessary to study this dinoflagellate to monitor HABs. In this study, 13 pairs of primers specific to P. donghaiense (within its internal transcribed spacer (ITS) regions) were designed for SYBR Green I real-time PCR. As the SYBR Green I real-time PCR could not identify P. donghaiense in a specific manner, a Taqman real-time PCR method was developed by designing a set of specific primers and a Taqman probe. A 10-fold serial dilution of recombinant plasmid containing ITS regions of P. donghaiense was prepared as standard samples and the standard curve was established. Additionally, we quantified the genomic DNA in P. donghaiense cells and utilized this DNA to prepare another 10-fold serial dilution of standard sample and accordingly set up the standard curve. The mathematic correlation between the cell number and its corresponding plasmid copy number was also established. In order to test the efficiency of the real-time PCR method, laboratory samples and P. donghaiense HAB field samples were employed for identification and quantitative analysis. As to laboratory samples, as few as 102 cells of P. donghaiense could be quantified precisely utilizing both centrifugation and filtration techniques. The quantification results from field samples by real-time PCR were highly similar to those by light microscopy. In conclusion, the real-time PCR could be applied to identify and quantify P. donghaiense in HABs. |
| Keywords: | Prorocentrum donghaiense Harmful Algal Blooms (HABs) internal transcribed spacer (ITS) recombinant plasmid real-time PCR |
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