Wenzhou Key Laboratory of Sanitary Microbiology, Key Laboratory of Laboratory Medicine, Ministry of Education, China, School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China 325035.
The Affiliated Kangning Hospital of Wenzhou Medical University, Wenzhou 325035, Zhejiang, China.
Harmful Algae. 2021 Mar;103:101996. doi: 10.1016/j.hal.2021.101996. Epub 2021 Feb 4.
Karenia mikimotoi is a toxic dinoflagellate that forms harmful blooms in coastal waters, threatening aquaculture worldwide. However, we do not know whether K. mikimotoi has a neurotoxic effect on aquatic animal behavior. Thus, this study investigated potential K. mikimotoi neurotoxicity in zebrafish larvae. Cells of K. mikimotoi were collected at the mid-exponential phase from a batch culture to prepare ruptured cell solutions (RCS). At 6 h post-fertilization (hpf), zebrafish embryos were exposed to different RCS concentrations (0, 10, 10, 10, and 2.5 × 10 cells mL). After 120 hpf, treated larvae were collected to analyze locomotor behavior; activities of acetylcholinesterase (AChE), superoxide dismutase (SOD), catalase (CAT); and expression of genes related to neurodevelopment. We found that RCS did not affect survival rate, but significantly decreased larval locomotion, as well as their AChE, SOD, and CAT activity. Additionally, the examination of the day-night behavioral experiment revealed RCS decreased locomotion only at night. Zebrafish larvae were also significantly hypoactive in response to light and sound stimulations. Of the neurodevelopment genes, three (th, neurog1, and neurod1) were downregulated, while two (bdnf and manf) were upregulated. Our study suggests that K. mikimotoi neurotoxicity occurs through causing oxidative damage, as well as disorders in the cholinergic system and nervous system development. The results provide new insight that K. mikimotoi in low abundance did not cause significant lethal effect but still exhibited significant neurotoxicity on aquatic animals.
米氏凯伦藻是一种产生赤潮的有毒甲藻,会对全球水产养殖业造成威胁。然而,我们并不清楚米氏凯伦藻是否会对水生动物的行为产生神经毒性。因此,本研究调查了米氏凯伦藻对斑马鱼幼虫的潜在神经毒性。从批量培养中收集处于指数中期的米氏凯伦藻细胞,以制备破裂细胞溶液(RCS)。在受精后 6 小时(hpf),将斑马鱼胚胎暴露于不同的 RCS 浓度(0、10、10、10 和 2.5×10 个细胞 mL)中。在 120 hpf 后,收集处理过的幼虫以分析运动行为;乙酰胆碱酯酶(AChE)、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)的活性;以及与神经发育相关基因的表达。我们发现 RCS 不会影响存活率,但会显著降低幼虫的运动能力,以及它们的 AChE、SOD 和 CAT 活性。此外,昼夜行为实验的检查表明,RCS 仅在夜间降低了运动能力。斑马鱼幼虫对光和声音刺激的反应也明显迟钝。在神经发育基因中,有三个(th、neurog1 和 neurod1)下调,而两个(bdnf 和 manf)上调。我们的研究表明,米氏凯伦藻的神经毒性是通过造成氧化损伤,以及胆碱能系统和神经系统发育紊乱而产生的。研究结果提供了新的见解,即低丰度的米氏凯伦藻不会造成显著的致死效应,但仍对水生动物表现出显著的神经毒性。