Tay Yi Juin, Liang Ji, Yao Shu, Han Mingming
Universiti Sains Malaysia, 11800, Minden, Penang, Malaysia.
Human Nutrition Research Centre, Newcastle University, Newcastle upon Tyne, UK.
Mar Biotechnol (NY). 2025 Jun 23;27(4):100. doi: 10.1007/s10126-025-10469-2.
Berberine hydrochloride (BH), the derivative component of Coptidis chinensis, is widely used to treat bacterial infections due to its notable antibacterial properties. However, the underlying molecular mechanisms of its therapeutic effects remain largely unexplored. This study employed transcriptome sequencing to investigate berberine hydrochloride's therapeutic efficacy and molecular responses in Branchiostoma belcheri infected with Aeromonas hydrophila. In this study, B. belcheri was first exposed to 200 mg/L berberine hydrochloride (BH) for 24 h, and then infected with A. hydrophila. After 48 h, transcriptome differential expression analysis was performed to compare the transcriptomic changes with the control group. A total of 2,478 differentially expressed genes (DEGs) were identified. Enrichment analysis revealed that these DEGs are involved in key pathways such as metabolism, cellular processes, signal transduction, and immune functions. Berberine hydrochloride treatment activated pathways including retinol metabolism, proteasome function, oxidative phosphorylation, lysosome, phagosome, and glutathione metabolism. RT-PCR validation confirmed the upregulation of immune-related genes such as TUBA, RAB5A, CTSL, GST, GPX4, G6PD, ND1, COX2, FECH, and LYP3A across these seven pathways. Notably, the glutathione metabolism, phagocytosis, and oxidative phosphorylation pathways appear to be central in regulating BH-mediated protection against A. hydrophila infection in B. belcheri. Moreover, BH significantly enhanced the activity of glutathione-related pathways, including GST, GSH, GPX, and GSSG in the hepatic caecum, activating oxidative defence systems and modulating immune-related responses in B. belcheri under A. hydrophila exposure. These results provide new insights into the potential role of BH in enhancing immune and oxidative stress responses in lancelets, which may have implications for its application in aquaculture.
盐酸小檗碱(BH)是黄连的衍生成分,因其显著的抗菌特性而被广泛用于治疗细菌感染。然而,其治疗效果的潜在分子机制在很大程度上仍未得到探索。本研究采用转录组测序来研究盐酸小檗碱对感染嗜水气单胞菌的文昌鱼的治疗效果和分子反应。在本研究中,首先将文昌鱼暴露于200mg/L盐酸小檗碱(BH)中24小时,然后感染嗜水气单胞菌。48小时后,进行转录组差异表达分析,以比较与对照组的转录组变化。共鉴定出2478个差异表达基因(DEG)。富集分析表明,这些DEG参与了代谢、细胞过程、信号转导和免疫功能等关键途径。盐酸小檗碱处理激活了包括视黄醇代谢、蛋白酶体功能、氧化磷酸化、溶酶体、吞噬体和谷胱甘肽代谢等途径。RT-PCR验证证实了这七条途径中免疫相关基因如TUBA、RAB5A、CTSL、GST、GPX4、G6PD、ND1、COX2、FECH和LYP3A的上调。值得注意的是,谷胱甘肽代谢、吞噬作用和氧化磷酸化途径似乎在调节BH介导的对文昌鱼嗜水气单胞菌感染的保护中起核心作用。此外,BH显著增强了肝盲囊中谷胱甘肽相关途径(包括GST、GSH、GPX和GSSG)的活性,激活了氧化防御系统,并在嗜水气单胞菌暴露下调节文昌鱼的免疫相关反应。这些结果为BH在增强文昌鱼免疫和氧化应激反应中的潜在作用提供了新的见解,这可能对其在水产养殖中的应用具有启示意义。