LOHABE, Department of Oceanography, Chonnam National University, Gwangju 61186, Republic of Korea.
LOHABE, Department of Oceanography, Chonnam National University, Gwangju 61186, Republic of Korea.
Harmful Algae. 2017 May;65:1-8. doi: 10.1016/j.hal.2017.04.002. Epub 2017 Apr 14.
Some marine dinoflagellates form ecdysal cyst (=temporary cysts) as part of their life cycle or under unfavorable growth conditions. Whether the dinoflagellates form ecdysal cysts or not may influence susceptibility to parasitism. In this study, parasite prevalence relative to inoculum size of the parasitoid Parvilucifera infectans zoospores for two dinoflagellate hosts (i.e., Fragilidium duplocampanaeforme and Dinophysis acuminata), which have different life cycle strategies, was examined. Further, susceptibility of cysts to parasitism, encystment signal, duration of encystments, and effects of induced encystment on diel periodicity, using ecdysal cyst-forming F. duplocampanaeforme were explored. The percent hosts infected by P. infectans plotted as a function of inoculum size showed a sharp increase to a maximum in D. acuminata, but a gradual linear rise in F. duplocampanaeforme: while the parasite prevalence in D. acuminata increased to a maximum of 78.8 (±2.4%) by a zoospore:host ratio of 20:1, it in F. duplocampanaeforme only reached 8.9 (±0.3%), even at a zoospore:host ratio of 120:1. In F. duplocampanaeforme, infections were observed only in the vegetative cells and not observed in ecdysal cysts. When exposed to live, frozen, and sonicated zoospores and zoospore filtrate, F. duplocampanaeforme formed ecdysal cysts only when exposed to live zoospores, suggesting that temporary cyst formation in the dinoflagellate resulted from direct contact with zoospores. When the Parvilucifera zoospores attacked and struggled to penetrate F. duplocampanaeforme through its flagellar pore, the Fragilidium cell shed all thecal plates, forming a 'thecal cloud layer', in which the zoospores were caught and immobilized and thus could not penetrate anymore. The duration (35±1.8h) of ecdysal cysts induced with addition of zoospores was significantly longer than that (15±0.8h) of normally formed cysts (i.e., without addition of zoospores), thereby resulting in delayed growth as well as influencing the pattern of diel periodicity. The results from this study suggest that in addition to the classical predator-prey interaction and allelopathic interaction, parasitism and its accompanying defense can make the food web dynamics much more complicated than previously thought.
一些海洋甲藻会形成蜕皮囊(=临时囊),这是它们生命周期的一部分,或者是在生长条件不利的情况下。甲藻是否形成蜕皮囊可能会影响其对寄生虫的易感性。在这项研究中,检查了两种不同生活史策略的甲藻宿主(即 Fragilidium duplocampanaeforme 和 Dinophysis acuminata)的寄生性 Parvilucifera infectans 游孢子的寄生虫患病率与接种物大小的关系。此外,还研究了蜕皮囊形成的 F. duplocampanaeforme 对寄生虫的易感性、囊形成信号、囊形成时间以及诱导囊形成对昼夜节律的影响。寄生感染 P. infectans 的宿主百分比作为接种物大小的函数绘制,在 D.acuminata 中急剧增加到最大值,但在 F.duplocampanaeforme 中逐渐呈线性上升:当 D.acuminata 中的寄生虫患病率达到最高 78.8(±2.4%)时,游孢子:宿主比为 20:1,而在 F.duplocampanaeforme 中,即使游孢子:宿主比为 120:1,也仅达到 8.9(±0.3%)。在 F.duplocampanaeforme 中,仅在营养细胞中观察到感染,而在蜕皮囊中未观察到感染。当暴露于活的、冷冻的和超声处理的游孢子和游孢子滤液时,F.duplocampanaeforme 仅在暴露于活的游孢子时才形成蜕皮囊,这表明甲藻的临时囊形成是由于与游孢子的直接接触。当 Parvilucifera 游孢子通过其鞭毛孔攻击并努力穿透 F.duplocampanaeforme 时, Fragilidium 细胞会脱落所有鞘板,形成“鞘板云层”,其中游孢子被捕获并固定,因此无法再穿透。添加游孢子诱导的蜕皮囊的持续时间(35±1.8h)明显长于正常形成的蜕皮囊(即未添加游孢子)的持续时间(15±0.8h),从而导致生长延迟,并影响昼夜节律模式。本研究的结果表明,除了经典的捕食者-猎物相互作用和化感相互作用外,寄生虫及其伴随的防御作用可以使食物网动态比以前想象的复杂得多。