Wen Jing, Liu Shuyao, Yang Bingbing, Tan Mingyue, Shen Xiuli, Du Zhiqiang
School of Life Science and Technology, Inner Mongolia University of Science and Technology, Baotou, Inner Mongolia autonomous region, 014010, China.
Library, Inner Mongolia University of Science and Technology, Baotou, Inner Mongolia autonomous region, 014010, China.
Dev Comp Immunol. 2025 Sep;170:105438. doi: 10.1016/j.dci.2025.105438. Epub 2025 Aug 6.
This study focused on peroxiredoxin (Prx) as a core target to investigate its regulatory mechanism in the innate immunity of Procambarus clarkii (crayfish). We observed that a reduction in the expression of prx 4 via injection of double-stranded RNA (dsRNA) induced early upregulation of HO levels in the hepatopancreas of crayfish. When the crayfish were subsequently infected with Vibrio harveyi, the HO levels further increased, and the antioxidant enzyme system was activated. After injecting dsPc-Prx 4 and subsequently stimulating the crayfish with V. harveyi, we observed upregulated expression of genes related to the melanization pathway, reactive oxygen species (ROS) pathway, apoptosis pathway, and Toll pathway. Furthermore, after the injection of dsPc-Prx 4 followed by V. harveyi and subsequent N-acetylcysteine (NAC) exposure, the expression of genes related to the melanization, apoptosis, and Toll pathways was downregulated; moreover, the melanization phenomenon was significantly weakened, and the survival rate of the crayfish decreased. The abovementioned experimental results demonstrate that Pc-Prx 4 is an important regulatory enzyme in the antioxidant system of crayfish. It can influence the antibacterial innate immune response of P. clarkii by modulating HO levels. This study provides a significant addition to the fundamental theory of antibacterial innate immunity in invertebrates and offers a theoretical basis for the prevention and control of bacterial diseases in P. clarkii.
本研究聚焦于过氧化物酶(Prx)这一核心靶点,以探究其在克氏原螯虾(小龙虾)先天免疫中的调控机制。我们观察到,通过注射双链RNA(dsRNA)降低prx 4的表达会诱导小龙虾肝胰腺中HO水平的早期上调。当小龙虾随后感染哈维氏弧菌时,HO水平进一步升高,且抗氧化酶系统被激活。在注射dsPc-Prx 4并随后用哈维氏弧菌刺激小龙虾后,我们观察到与黑化途径、活性氧(ROS)途径、凋亡途径和Toll途径相关的基因表达上调。此外,在注射dsPc-Prx 4后再用哈维氏弧菌刺激,随后进行N-乙酰半胱氨酸(NAC)处理,与黑化、凋亡和Toll途径相关的基因表达下调;此外,黑化现象显著减弱,小龙虾的存活率降低。上述实验结果表明,Pc-Prx 4是小龙虾抗氧化系统中的一种重要调节酶。它可以通过调节HO水平影响克氏原螯虾的抗菌先天免疫反应。本研究为无脊椎动物抗菌先天免疫的基础理论增添了重要内容,并为克氏原螯虾细菌性疾病的防控提供了理论依据。