Gao Yangchun, Fang Hongda, Dong Yanhong, Li Haitao, Pu Chuanliang, Zhan Aibin
Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, China.
University of Chinese Academy of Sciences, Chinese Academy of Sciences, Beijing, China.
PeerJ. 2017 Apr 26;5:e3224. doi: 10.7717/peerj.3224. eCollection 2017.
Dinoflagellate cysts (i.e., dinocysts) are biologically and ecologically important as they can help dinoflagellate species survive harsh environments, facilitate their dispersal and serve as seeds for harmful algal blooms. In addition, dinocysts derived from some species can produce more toxins than vegetative forms, largely affecting species through their food webs and even human health. Consequently, accurate identification of dinocysts represents the first crucial step in many ecological studies. As dinocysts have limited or even no available taxonomic keys, molecular methods have become the first priority for dinocyst identification. However, molecular identification of dinocysts, particularly when using single cells, poses technical challenges. The most serious is the low success rate of PCR, especially for heterotrophic species.
In this study, we aim to improve the success rate of single dinocyst identification for the chosen dinocyst species (, , , and ) distributed in the South China Sea. We worked on two major technical issues: cleaning possible PCR inhibitors attached on the cyst surface and designing new dinoflagellate-specific PCR primers to improve the success of PCR amplification.
For the cleaning of single dinocysts separated from marine sediments, we used ultrasonic wave-based cleaning and optimized cleaning parameters. Our results showed that the optimized ultrasonic wave-based cleaning method largely improved the identification success rate and accuracy of both molecular and morphological identifications. For the molecular identification with the newly designed dinoflagellate-specific primers (18S634F-18S634R), the success ratio was as high as 86.7% for single dinocysts across multiple taxa when using the optimized ultrasonic wave-based cleaning method, and much higher than that (16.7%) based on traditional micropipette-based cleaning.
The technically simple but robust method improved on in this study is expected to serve as a powerful tool in deep understanding of population dynamics of dinocysts and the causes and consequences of potential negative effects caused by dinocysts.
甲藻孢囊(即藻孢囊)在生物学和生态学上具有重要意义,因为它们可以帮助甲藻物种在恶劣环境中生存,促进其扩散,并作为有害藻华的种子。此外,某些物种的藻孢囊产生的毒素比营养体形式更多,在很大程度上通过食物网影响物种,甚至影响人类健康。因此,准确鉴定藻孢囊是许多生态研究的关键第一步。由于藻孢囊的分类学关键有限甚至没有,分子方法已成为藻孢囊鉴定的首要选择。然而,藻孢囊的分子鉴定,特别是使用单细胞时,存在技术挑战。最严重的是PCR成功率低,尤其是对于异养物种。
在本研究中,我们旨在提高分布于中国南海的选定藻孢囊物种(、、、和)的单细胞鉴定成功率。我们致力于两个主要技术问题:清除附着在孢囊表面的可能的PCR抑制剂,以及设计新的甲藻特异性PCR引物以提高PCR扩增的成功率。
对于从海洋沉积物中分离出的单个藻孢囊的清洗,我们使用基于超声波的清洗并优化了清洗参数。我们的结果表明,优化后的基于超声波的清洗方法大大提高了分子和形态鉴定的成功率和准确性。对于使用新设计的甲藻特异性引物(18S634F - 18S634R)进行的分子鉴定,当使用优化后的基于超声波的清洗方法时,多个分类群的单个藻孢囊的成功率高达86.7%,远高于基于传统微量移液器清洗的成功率(16.7%)。
本研究改进的技术简单但稳健的方法有望成为深入了解藻孢囊种群动态以及藻孢囊潜在负面影响的原因和后果的有力工具。