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Host and Symbiont Cell Cycle Coordination Is Mediated by Symbiotic State, Nutrition, and Partner Identity in a Model Cnidarian-Dinoflagellate Symbiosis

机译:宿主和分析细胞周期协调是由共生状态,营养和伴侣身份介导的患有CNIDARIAR-DINOFLAGLEATE Sysfisis

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The cell cycle is a critical component of cellular proliferation, differentiation, and response to stress, yet its role in the regulation of intracellular symbioses is not well understood. To explore host-symbiont cell cycle coordination in a marine symbiosis, we employed a model for coral-dinoflagellate associations: the tropical sea anemone Aiptasia ( Exaiptasia pallida ) and its native microalgal photosymbionts ( Breviolum minutum and Breviolum psygmophilum ). Using fluorescent labeling and spatial point-pattern image analyses to characterize cell population distributions in both partners, we developed protocols that are tailored to the three-dimensional cellular landscape of a symbiotic sea anemone tentacle. Introducing cultured symbiont cells to symbiont-free adult hosts increased overall host cell proliferation rates. The acceleration occurred predominantly in the symbiont-containing gastrodermis near clusters of symbionts but was also observed in symbiont-free epidermal tissue layers, indicating that the presence of symbionts contributes to elevated proliferation rates in the entire host during colonization. Symbiont cell cycle progression differed between cultured algae and those residing within hosts; the endosymbiotic state resulted in increased S-phase but decreased G _(2)/M-phase symbiont populations. These phenotypes and the deceleration of cell cycle progression varied with symbiont identity and host nutritional status. These results demonstrate that host and symbiont cells have substantial and species-specific effects on the proliferation rates of their mutualistic partners. This is the first empirical evidence to support species-specific regulation of the symbiont cell cycle within a single cnidarian-dinoflagellate association; similar regulatory mechanisms likely govern interpartner coordination in other coral-algal symbioses and shape their ecophysiological responses to a changing climate.
机译:细胞周期是细胞增殖,分化和对应激的反应的关键组分,但其在细胞内Symbiase的调节中的作用尚不清楚。为了在海洋共生中探索宿主 - 共生细胞周期协调,我们使用了珊瑚堇青树协会的模型:热带海葵Aiptasia(Exapiparasia pallida)及其天然微藻(Breviolum minutum和Breviolum psygmophilum)。使用荧光标记和空间点图案图像分析,以表征两个合作伙伴中的细胞群分布,我们开发了针对共生海葵触手的三维蜂窝景观量身定制的协议。将培养的Symbiont细胞引入与Symbiont的成人宿主增加总体宿主细胞增殖率。加速度主要发生在含有Symbiont的胃肠杆菌中,靠近Symbionts的簇,但也观察到在Symbiont的表皮组织层中观察到,表明在定子期间,共生的存在有助于整个宿主的升高的增殖速率。 Symbiont细胞周期进展不同于培养的藻类和居住在主机内的那些;内胞生物状态导致S相增加,但G _(2)/ m相分析群体增加。这些表型和细胞周期的减速随Smitbiont身份和宿主状态而变化。这些结果表明,宿主和共生细胞对其相互融合伙伴的增殖率具有大量和物种特异性影响。这是第一个支持单一CNIDAR-DINOFLAGLAGENCE联想中Symbiont细胞周期的特异性调节的第一证据证据;类似的监管机制可能对其他珊瑚藻类合作社的互补者协调进行治理,并将其生态学反应塑造变化的气候。

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