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造礁石珊瑚共生藻的快速热适应。

Rapid thermal adaptation in photosymbionts of reef-building corals.

机构信息

Australian Institute of Marine Science, Townsville, Qld, Australia.

College of Marine and Environmental Sciences, James Cook University, Townsville, Qld, Australia.

出版信息

Glob Chang Biol. 2017 Nov;23(11):4675-4688. doi: 10.1111/gcb.13702. Epub 2017 Apr 27.

Abstract

Climate warming is occurring at a rate not experienced by life on Earth for 10 s of millions of years, and it is unknown whether the coral-dinoflagellate (Symbiodinium spp.) symbiosis can evolve fast enough to ensure coral reef persistence. Coral thermal tolerance is partly dependent on the Symbiodinium hosted. Therefore, directed laboratory evolution in Symbiodinium has been proposed as a strategy to enhance coral holobiont thermal tolerance. Using a reciprocal transplant design, we show that the upper temperature tolerance and temperature tolerance range of Symbiodinium C1 increased after ~80 asexual generations (2.5 years) of laboratory thermal selection. Relative to wild-type cells, selected cells showed superior photophysiological performance and growth rate at 31°C in vitro, and performed no worse at 27°C; they also had lower levels of extracellular reactive oxygen species (exROS). In contrast, wild-type cells were unable to photosynthesise or grow at 31°C and produced up to 17 times more exROS. In symbiosis, the increased thermal tolerance acquired ex hospite was less apparent. In recruits of two of three species tested, those harbouring selected cells showed no difference in growth between the 27 and 31°C treatments, and a trend of positive growth at both temperatures. Recruits that were inoculated with wild-type cells, however, showed a significant difference in growth rates between the 27 and 31°C treatments, with a negative growth trend at 31°C. There were no significant differences in the rate and severity of bleaching in coral recruits harbouring wild-type or selected cells. Our findings highlight the need for additional Symbiodinium genotypes to be tested with this assisted evolution approach. Deciphering the genetic basis of enhanced thermal tolerance in Symbiodinium and the cause behind its limited transference to the coral holobiont in this genotype of Symbiodinium C1 are important next steps for developing methods that aim to increase coral bleaching tolerance.

摘要

气候变暖正以数千万年来地球上生命从未经历过的速度发生,而珊瑚-虫黄藻(Symbiodinium spp.)共生体是否能进化得足够快以确保珊瑚礁的持续存在尚不清楚。珊瑚的热耐受性部分取决于其所携带的共生藻。因此,人们提出了在共生藻中进行定向实验室进化的策略,以增强珊瑚整体的热耐受性。通过往返移植设计,我们发现 Symbiodinium C1 的上限温度耐受性和温度耐受范围在经过约 80 代(2.5 年)的实验室热选择后增加。与野生型细胞相比,选择的细胞在体外 31°C 时表现出更好的光生理性能和生长速率,在 27°C 时表现不差;它们还具有较低水平的细胞外活性氧物质(exROS)。相比之下,野生型细胞无法在 31°C 下进行光合作用或生长,并且产生的 exROS 多达 17 倍。在共生关系中,从宿主体内获得的增加的热耐受性不太明显。在所测试的三个物种中的两个中,那些携带选择细胞的珊瑚幼虫在 27°C 和 31°C 处理之间的生长没有差异,并且在两个温度下都呈现出正增长趋势。然而,那些接种了野生型细胞的珊瑚幼虫在 27°C 和 31°C 处理之间的生长率存在显著差异,在 31°C 时呈现负增长趋势。在携带野生型或选择细胞的珊瑚幼虫中,白化的速度和严重程度没有差异。我们的研究结果强调需要对更多的共生藻基因型进行测试,以采用这种辅助进化方法。解析 Symbiodinium 中增强的热耐受性的遗传基础,以及这种热耐受性在这种 Symbiodinium C1 基因型中对珊瑚整体的有限转移的原因,是开发旨在提高珊瑚白化耐受性的方法的重要下一步。

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