Integrated Analysis of Physiological, Histological, and Transcriptomic Responses to Transport Density in Schizothorax nukiangensis

IF 2.8 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jinlin Wang, Yuting Duan, Dapeng Gu, Hejiao Li, Luo Lei, Ning Wang, Wenjia He, Yinhua Zhou, Rongrong Liao, Mei Peng, Xinyu Liu, Zhaofang Han, Haiping Liu, Chaowei Zhou, Benhe Zeng
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Abstract

Transport density is a pivotal regulatory factor during live fish transport, as it determines the intensity of stress responses and subsequent survival. With increasing demands for artificial propagation, stock enhancement, and scientific research, the frequency of transporting Schizothorax nukiangensis has risen substantially. This study evaluated the effects of different transport densities (100, 150, and 200 kg/m3) after 4 h on water quality, plasma biochemistry, tissue morphology, and transcriptional responses. High-density transport elevated ammonia nitrogen and temperature, reduced pH, and caused mortality in the highest-density group. Gill and liver tissues exhibited progressive structural damage, accompanied by increased plasma ROS, SOD, cortisol, and glucose levels, while IgG, CAT and T-AOC decreased under higher densities. Transcriptomic analyses showed that upregulated DEGs in the gill were primarily enriched in Antigen processing and presentation, whereas innate immune pathways—including RIG-I-like receptor, IL-17, and cytosolic DNA-sensing—were suppressed. This pattern suggests that increasing transport density suppresses innate immune responses, thereby shifting immune regulation toward enhanced adaptive immune activation via antigen processing and presentation. Both gill and liver exhibited pronounced enrichment of lipid metabolism–related pathways—including steroid biosynthesis, fatty acid metabolism, glycerolipid metabolism, and fat digestion and absorption—accompanied by extensive upregulation of these genes. These changes are tightly associated with activation of the PPAR signaling pathway, which facilitates fatty acid transport, degradation, and β-oxidation, thus sustaining energy supply under transport-induced stress. These findings clarify the physiological and molecular mechanisms of transport stress in S. nukiangensis and provide guidance for optimizing short-distance transport strategies.

nukiangschizothorax nukiangensis生理、组织学和转录组学对转运密度的综合分析。
运输密度是活鱼运输过程中的关键调控因素,因为它决定了应激反应的强度和随后的存活。随着人工繁殖、种群增养和科学研究等需求的增加,努江裂胸鱼的运输频率大幅上升。本研究评估了不同输运密度(100、150和200 kg/m3) 4 h后对水质、血浆生化、组织形态和转录反应的影响。高密度转运使氨氮和温度升高,pH值降低,并导致最高密度组的死亡。鳃和肝组织表现出进行性结构损伤,伴随着血浆ROS、SOD、皮质醇和葡萄糖水平升高,而IgG、CAT和T-AOC在高密度下下降。转录组学分析显示,鳃中上调的deg主要富集于抗原加工和呈递中,而先天免疫途径(包括rig -i样受体、IL-17和胞质dna传感)则受到抑制。这种模式表明,增加转运密度会抑制先天免疫反应,从而将免疫调节转向通过抗原加工和递呈增强适应性免疫激活。鳃和肝脏均表现出脂质代谢相关途径的显著富集,包括类固醇生物合成、脂肪酸代谢、甘油脂代谢、脂肪消化和吸收,并伴有这些基因的广泛上调。这些变化与PPAR信号通路的激活密切相关,PPAR信号通路促进脂肪酸的运输、降解和β-氧化,从而在运输诱导的应激下维持能量供应。这些研究结果阐明了女足转运胁迫的生理和分子机制,为优化短距离转运策略提供了指导。
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来源期刊
Marine Biotechnology
Marine Biotechnology 工程技术-海洋与淡水生物学
CiteScore
4.80
自引率
3.30%
发文量
95
审稿时长
2 months
期刊介绍: Marine Biotechnology welcomes high-quality research papers presenting novel data on the biotechnology of aquatic organisms. The journal publishes high quality papers in the areas of molecular biology, genomics, proteomics, cell biology, and biochemistry, and particularly encourages submissions of papers related to genome biology such as linkage mapping, large-scale gene discoveries, QTL analysis, physical mapping, and comparative and functional genome analysis. Papers on technological development and marine natural products should demonstrate innovation and novel applications.
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