College of Earth, Ocean, and Environment, University of Delaware, 700 Pilottown Road, Lewes, DE 19958, USA.
Biomaging Center, Delaware Biotechnology Institute, University of Delaware, 15 Innovation Way, Newark, DE 19711, USA.
Harmful Algae. 2017 Feb;62:127-135. doi: 10.1016/j.hal.2016.12.004. Epub 2017 Jan 16.
The algicide, IRI-160AA, induces mortality in dinoflagellates but not other species of algae, suggesting that a shared characteristic or feature renders this class of phytoplankton vulnerable to the algicide. In contrast to other eukaryotic species, the genome of dinoflagellates is stabilized by high concentrations of divalent cations and transition metals and contains large amounts of DNA with unusual base modifications. These distinctions set dinoflagellates apart from other phytoplankton and suggest that the nucleus may be a dinoflagellate-specific target for IRI-160AA. In this study, morphological and ultrastructural changes in three dinoflagellate species, Prorocentrum minimum, Karlodinium veneficum and Gyrodinium instriatum, were evaluated after short-term exposure to IRI-160AA using super resolution structured illumination microscopy (SR-SIM) and transmission electron microscopy (TEM). Exposure to the algicide resulted in cytoplasmic membrane blebbing, differing chloroplast morphologies, nuclear expansion, and chromosome expulsion and/or destabilization. TEM analysis showed that chromosomes of algicide-treated K. veneficum appeared electron dense with fibrous protrusions. In algicide-treated P. minimum and G. instriatum, chromosome decompaction occurred, while for P. minimum, nuclear expulsion was also observed for several cells. Results of this investigation demonstrate that exposure to the algicide destabilizes dinoflagellate chromosomes, although it was not clear if the nucleus was the primary target of the algicide or if the observed effects on chromosomal structure were due to downstream impacts. In all cases, changes in cellular morphology and ultrastructure were observed within two hours, suggesting that the algicide may be an effective and rapid approach to mitigate dinoflagellate blooms.
杀藻剂 IRI-160AA 可诱导甲藻死亡,但不影响其他藻类,这表明甲藻类浮游生物具有某种共同特征,使它们易受杀藻剂影响。与其他真核生物不同,甲藻的基因组通过二价阳离子和过渡金属的高浓度稳定,并含有大量具有异常碱基修饰的 DNA。这些区别使甲藻与其他浮游生物区别开来,并表明细胞核可能是 IRI-160AA 针对甲藻的特异性靶标。在这项研究中,使用超分辨率结构光照显微镜 (SR-SIM) 和透射电子显微镜 (TEM) 评估了三种甲藻(微小原甲藻、卡盾藻和旋沟藻)在短期暴露于 IRI-160AA 后的形态和超微结构变化。杀藻剂暴露导致质膜起泡、不同的叶绿体形态、核扩张以及染色体排出和/或不稳定。TEM 分析表明,经杀藻剂处理的卡盾藻染色体呈电子致密状,带有纤维状突起。在经杀藻剂处理的微小原甲藻和旋沟藻中,染色体解压缩,而在微小原甲藻中,也观察到几个细胞的核排出。本研究结果表明,暴露于杀藻剂会使甲藻染色体不稳定,尽管尚不清楚细胞核是否是杀藻剂的主要靶标,或者观察到的染色体结构变化是否是由于下游影响所致。在所有情况下,都在两小时内观察到细胞形态和超微结构的变化,这表明杀藻剂可能是一种有效且快速的方法来减轻甲藻水华。