果寡糖对姬蛙水单胞菌诱导的氧化应激和细胞凋亡的保护作用

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BMC Genomics Pub Date : 2024-10-17 DOI:10.1186/s12864-024-10881-3
Chunnuan Zhang, Dongxue Jiang, Huajuan Shi, Cheng Zhang, Feng Yang, Qian Qi, Ruiyi Xu
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引用次数: 0

摘要

本研究旨在探讨膳食果寡糖(FOS)对钝吻鳊(Megalobrama amblycephala)嗜水气单胞菌(A. hydrophila)诱导的氧化应激和细胞凋亡的影响。鱼类分为以下三组:C1(对照组)、T1(蚜茧蜂)和 T2(蚜茧蜂 + 4 g/kg FOS)。结果表明,蚜茧蜂感染导致抗氧化酶活性增加,肝脏形态排列紊乱,细胞大面积坏死。而膳食纤维素能改善上述肝损伤。此外,FOS还提高了促凋亡分子(包括caspase-8和9)的mRNA水平,并下调了抗凋亡分子Bcl-2的mRNA水平。转录组分析表明,鳗鲡感染钝口鳊后,肠道中与氧化应激相关的 DEGs 通路被激活。添加 FOS 的组别富集了更多的健康通路。进一步的WGCNA共表达网络分析显示,筛选出的单个基因被聚类为49个模块。结合生理生化特征,选择与五个性状关联度最高的两个模块(10 个中枢基因)构建网络。综上所述,本研究为探索食源性 FOS 中的亲水藻类修复基因奠定了基础,也为今后的水产养殖奠定了理论基础。
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Protective effect of fructooligosaccharide against oxidative stress and apoptosis induced by Aeromonas hydrophila in Megalobrama amblycephala.

This research aimed to investigate the effects of dietary fructooligosaccharides (FOS) on attenuating the Aeromonas hydrophila (A. hydrophila)-induced oxidative stress and apoptosis in blunt snout bream Megalobrama amblycephala. Fish were divided into three groups as follows: C1 (Control), T1 (A. hydrophila), and T2 (A. hydrophila + 4 g/kg FOS). The results showed that the activities of antioxidant enzymes increased, the liver morphology had disorderly arrangement, and extensive cell necrosis occurred because of A. hydrophila-infection. While the dietary FOS improved the above-mentioned liver damage. Additionaly, FOS elevated mRNA levels of pro-apoptotic molecules, including caspase-8 and 9, and down-regulated mRNA levels of the anti-apoptotic molecule Bcl-2, which is triggered by A. hydrophila-infection. The transcriptome analysis showed that the oxidative stress-related DEGs pathways were activated in intestine of blunt snout bream by A. hydrophila-infection. The FOS-added group led to the enrichment of more pathways to health. Further WGCNA co-expression network analysis showed that the screened single genes were clustered into 49 modules. The two modules with the highest association to the five traits (10 hub genes) were chosen to build the network by combining the physiological and biochemical characteristic. In summary, this research offers a foundation for the exploring of A. hydrophila-restoration genes in dietary FOS, and also lays a theoretical foundation for aquaculture in the future.

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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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