从转录组深入了解高温条件下弧菌诱发蛤蜊死亡的情况

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Li Dong , Jiajia Yu , Hongxia Wang , Xin Yue , Baozhong Liu
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引用次数: 0

摘要

在这项研究中,我们调查了蛤蜊 Meretrix petechialis 在不同温度下面对弧菌挑战时的死亡率及其潜在的分子机制。我们的实验清楚地表明,蛤蜊的死亡主要是在高温条件下观察到的,这凸显了热应力对蛤蜊感染易感性的关键影响。利用 RNA-seq,我们进一步比较了蛤鳃在高温和低温下对弧菌的全局转录反应。与其他组相比,高温下弧菌感染组的差异表达基因与免疫、氧化应激和膜转运有关。主要结果显示,高温下蛤蜊的免疫反应减弱,尤其是 TNF 信号通路,膜运输效率降低,特别是 SLC 蛋白。此外,高温增强了与促炎相关的不饱和脂肪酸代谢,导致氧化损伤增加。我们的生化检测进一步证明了这一点,高温下蛤蜊的脂质过氧化和蛋白质羰基化水平明显升高,表明氧化损伤加剧。对所选 DEGs 的 RT-PCR 验证证实了 RNA-seq 的发现。我们的研究结果有助于理解夏季贝类更频繁死亡的原因,强调了温度在病原体反应中的作用,阐明了病原体和高温胁迫协同效应的分子机制。所发现的关键基因为抗性辅助育种提供了潜在目标。这项研究对双壳类水产养殖及其生理学具有重要意义,尤其是在全球气候变化影响海洋生态系统的情况下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Transcriptomic insights into vibrio-induced mortality in the clam Meretrix petechialis under high temperature

Transcriptomic insights into vibrio-induced mortality in the clam Meretrix petechialis under high temperature

In this study, we investigate the mortality of the clam Meretrix petechialis facing a vibrio challenge under different temperatures and the underlying molecular mechanisms. Our experiment distinctly revealed that clam mortality was predominantly observed under high temperature, highlighting the critical impact of thermal stress on clam susceptibility to infection. Using RNA-seq, we further compared the global transcriptional response to vibrio in clam gills between high and low temperatures. Compared to other groups, the differentially expressed genes in vibrio-challenged group at high temperature associated with immunity, oxidative stress, and membrane transport. Key results show a weakened immune response in clams at high temperature, especially in the TNF signaling pathway, and a decrease in membrane transport efficiency, notably in SLC proteins. Additionally, high temperature enhanced pro-inflammatory related unsaturated fatty acid metabolism, leading to increased oxidative damage. This was further evidenced by our biochemical assays, which showed significantly higher levels of lipid peroxidation and protein carbonylation in clams at high temperature, indicating heightened oxidative damage. RT-PCR validation of selected DEGs corroborated the RNA-seq findings. Our findings contribute to the understanding of more frequent shellfish mortality in summer, emphasizing the role of temperature in pathogen response, elucidating the molecular mechanisms underlying the synergistic effect of pathogen and high temperature stresses. The key genes identified provide potential targets for resistance-assisted breeding. This research has significant implications for bivalve aquaculture and their physiology, particularly in light of global climate changes affecting marine ecosystems.

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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
69
审稿时长
33 days
期刊介绍: Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology. Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.
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