Thermal fluctuations independently modulate physiological plasticity and the dynamics of the gut microbiome in a tropical rocky shore oyster

IF 1.8 3区 生物学 Q3 ECOLOGY
Bovern Suchart Arromrak , Adrian Tsz Chun Wong , Tin Yan Hui , Kin Sum Leung , Gray A. Williams , Monthon Ganmanee , Thierry Durand , Jetty Chung-Yung Lee , Juan D. Gaitan-Espitia
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Abstract

Extreme high thermal conditions on tropical rocky shores are challenging to the survival of intertidal ectotherms. Yet, many species are highly successful in these environments in part due to their ability to regulate intrinsic mechanisms associated with physiological stress and their metabolic demand. More recently, there has been a growing awareness that other extrinsic mechanisms, such as animal-associated microbial communities, can also influence the tolerance and survival of ectotherms under stressful conditions. However, the extent to which the intrinsic and extrinsic mechanisms are functionally linked as part of the overall adaptive response of intertidal animals to temperature change and stress is poorly understood. Here, we examined the dynamics and potential interactions of intrinsic and extrinsic mechanisms in the tropical high-supratidal oyster, Isognomon nucleus. We found that oysters modulate their internal biochemistry (oxidized PUFA products, including 5-F2t-IsoP, 10-F4t-NeuroP, 13-F4t-NeuroP, and 16-F1t-PhytoP) as part of their adaptive regulation to cope with physiological stress during periods of extreme high temperatures when emersed. However, while we detected variation in alpha diversity (ASV richness and Shannon diversity index), dominant microbial taxa and microbial functions across time, no association was found with the host biochemical profiles. The findings here suggest that the thermal condition within oysters can independently influence their intrinsic biochemical responses and extrinsic microbiome profiles. Together, these mechanisms may contribute to the thermal tolerance and survival of the oysters in the challenging conditions of the tropical high-supratidal zone.

热波动独立调节热带岩岸牡蛎的生理可塑性和肠道微生物群动态
热带岩石海岸的极端高热条件对潮间带外温动物的生存构成了挑战。然而,许多物种之所以能在这些环境中取得巨大成功,部分原因是它们有能力调节与生理压力和新陈代谢需求相关的内在机制。最近,人们越来越意识到,其他外在机制(如动物相关微生物群落)也会影响外温动物在压力条件下的耐受性和存活率。然而,潮间带动物对温度变化和压力的整体适应性反应中,内在和外在机制在多大程度上存在功能上的联系,目前还知之甚少。在这里,我们研究了热带高潮位牡蛎(Isognomon nucleus)的内在和外在机制的动态和潜在相互作用。我们发现,牡蛎会调节其内部生物化学(氧化的 PUFA 产物,包括 5-F2t-IsoP、10-F4t-NeuroP、13-F4t-NeuroP 和 16-F1t-PhytoP),作为其适应性调节的一部分,以应对浸没在极端高温期间的生理压力。然而,虽然我们发现α多样性(ASV丰富度和香农多样性指数)、优势微生物类群和微生物功能在不同时期存在差异,但没有发现与宿主生化特征有关。研究结果表明,牡蛎体内的热条件可独立影响其内在生化反应和外在微生物组特征。这些机制共同作用,可能有助于牡蛎在热带高潮上带的挑战性条件下耐热和生存。
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来源期刊
Journal of Experimental Marine Biology and Ecology
Journal of Experimental Marine Biology and Ecology 生物-海洋与淡水生物学
CiteScore
4.30
自引率
0.00%
发文量
98
审稿时长
14 weeks
期刊介绍: The Journal of Experimental Marine Biology and Ecology provides a forum for experimental ecological research on marine organisms in relation to their environment. Topic areas include studies that focus on biochemistry, physiology, behavior, genetics, and ecological theory. The main emphasis of the Journal lies in hypothesis driven experimental work, both from the laboratory and the field. Natural experiments or descriptive studies that elucidate fundamental ecological processes are welcome. Submissions should have a broad ecological framework beyond the specific study organism or geographic region. Short communications that highlight emerging issues and exciting discoveries within five printed pages will receive a rapid turnaround. Papers describing important new analytical, computational, experimental and theoretical techniques and methods are encouraged and will be highlighted as Methodological Advances. We welcome proposals for Review Papers synthesizing a specific field within marine ecology. Finally, the journal aims to publish Special Issues at regular intervals synthesizing a particular field of marine science. All printed papers undergo a peer review process before being accepted and will receive a first decision within three months.
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