低盐度对Chromis notata渗透调节、氧化应激和微生物破坏的影响(Temminck & Schlegel, 1843)。

IF 1.9 3区 生物学 Q1 ZOOLOGY
Jin A Kim, Ji Yong Choi, Seul Hee Lee, Cheol Young Choi
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引用次数: 0

摘要

气候变化导致海洋环境发生重大变化,包括冰川融化导致的盐度降低、降雨增加和淡水流入,这些都对海洋生物造成压力。低渗应激导致活性氧的产生增加,从而破坏海洋鱼类的生理过程,如渗透调节、氧化反应和肠道微生物稳定性。为了更好地了解低盐对渗透调节、氧化应激和肠道微生物群的影响,我们研究了低盐雀鲷Chromis notata在低盐条件下(27和20 psu)的反应。通过测定血浆渗透压和鳃组织中Na+/K+- atp酶(NKA)活性来评估渗透调节的变化。血浆过氧化氢(H₂O₂)水平和脂质过氧化(LPO)水平作为氧化应激标志物进行测量。此外,通过16S rRNA测序和RNA测序,分别分析肠道微生物多样性和转录组反应。低盐度条件下,血浆渗透压和NKA活性显著降低,而H₂O₂和LPO水平显著升高。低盐度组的肠道微生物组α-多样性降低,变形菌属(包括致病属)丰度增加,而乳酸杆菌丰度降低。上调的基因与免疫和炎症反应有关,包括补体激活和盐跨膜转运蛋白活性,而下调的基因与侧质膜和线粒体膜有关。这些发现表明,低肾上腺素可诱导氧化应激,破坏草芥肠道微生物群的稳定性,从而引发复杂的生理和分子反应。这些发现为了解沿海和海洋生态系统中海洋鱼类因气候变化而面临的挑战提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Hyposalinity on Osmoregulation, Oxidative Stress, and Microbial Disruption in Chromis notata (Temminck & Schlegel, 1843).

Climate change causes substantial alterations in marine environments, including salinity reduction due to glacial melting, increased rainfall, and freshwater influx, which impose stress on marine organisms. Hypoosmotic stress leads to increased production of reactive oxygen species, thereby disrupting physiological processes, such as osmoregulation, oxidative responses, and gut microbial stability, in marine fish. Here, we investigated the responses of Chromis notata, a stenohaline damselfish, exposed to hyposaline conditions (27 and 20 psu), to better understand the effects of hyposalinity on osmoregulation, oxidative stress, and gut microbiota. Plasma osmolality was measured alongside Na+/K+-ATPase (NKA) activity in gill tissue to assess osmoregulatory changes. The plasma levels of hydrogen peroxide (H₂O₂) and lipid peroxidation (LPO) levels were measured as oxidative stress markers. Furthermore, 16S rRNA sequencing and RNA sequencing were conducted to analyze gut microbial diversity and transcriptomic responses, respectively. Plasma osmolality and NKA activity markedly decreased, whereas H₂O₂ and LPO levels remarkably increased under low-salinity conditions. The gut microbiome in the low-salinity groups exhibited decreased α-diversity and increased abundance of Proteobacteria, including pathogenic genera, whereas Lactobacillus abundance was reduced. Upregulated genes were associated with immune and inflammatory responses, including complement activation, and salt transmembrane transporter activity, whereas downregulated genes were linked to the lateral plasma membrane and mitochondrial membrane. These findings suggest that hyposaline induces oxidative stress and disrupts gut microbiome stability in C. notata, thereby triggering complex physiological and molecular responses. These findings provide insights into the challenges encountered by marine fish in coastal and oceanic ecosystems due to climate change.

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来源期刊
Journal of experimental zoology. Part A, Ecological and integrative physiology
Journal of experimental zoology. Part A, Ecological and integrative physiology Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
4.90
自引率
3.60%
发文量
0
期刊介绍: The Journal of Experimental Zoology – A publishes articles at the interface between Development, Physiology, Ecology and Evolution. Contributions that help to reveal how molecular, functional and ecological variation relate to one another are particularly welcome. The Journal publishes original research in the form of rapid communications or regular research articles, as well as perspectives and reviews on topics pertaining to the scope of the Journal. Acceptable articles are limited to studies on animals.
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