Cha Gui-Hong, Wang Wei-Na, Peng Ting, Huang Ming-Zhu, Liu Yuan
Key Laboratory of Ecology and Environmental Science in Guangdong Higher Education, Guangdong Provincial Key Laboratory for Healthy and Safe Aquaculture, College of Life Science, South China Normal University, Guangzhou 510631, China.
Key Laboratory of Ecology and Environmental Science in Guangdong Higher Education, Guangdong Provincial Key Laboratory for Healthy and Safe Aquaculture, College of Life Science, South China Normal University, Guangzhou 510631, China.
Dev Comp Immunol. 2015 Aug;51(2):226-37. doi: 10.1016/j.dci.2015.04.004. Epub 2015 Apr 16.
The small GTPase Rac1 acts as a molecular switch for signal transduction that regulates various cellular functions. However, its functions in crustaceans remain unclear. In this study, a cDNA encoding a RAS GTPase (LvRac1) in the Pacific white shrimp (L. vannamei) was identified and characterized. A recombinant variant of this GTPase, rLvRac1, was expressed in the model organism P. pastoris and its expression was confirmed by mass spectrometry. Biochemical assays indicated that the recombinant protein retained GTPase activity and was expressed in all of the organism's tested tissues. Injection of the bacterium V. alginolyticus into L. vannamei induced hepatopancreatic upregulation of LvRac1 expression. Moreover, knocking down LvRac1 in vivo significantly reduced the expression of the L. vannamei p53 and Cu/Zn superoxide dismutase genes (Lvp53 and LvCu/Zn SOD, respectively) while increasing that of the galectin gene (Lvgal). Hemolymph samples from control and LvRac1-silenced L. vannamei individuals were analyzed by flow cytometry, revealing that the latter exhibited significantly reduced respiratory burst activity and total hemocyte counts. Cumulative mortality in shrimp lacking LvRac1 was significantly greater than in control groups following V. alginolyticus challenge. The silencing of LvRac1 by double-stranded RNA injection thus increased the V. alginolyticus challenge sensitivity of L. vannamei and weakened its bacterial clearance ability in vivo. Suppressing LvRac1 also promoted the upregulation of Lvp53, LvCu/ZnSOD, and Lvgal following V. alginolyticus injection. Taken together, these results suggest that LvRac1 is important in the innate immune response of shrimp to V. alginolyticus infection.
小GTP酶Rac1作为信号转导的分子开关,调节各种细胞功能。然而,其在甲壳类动物中的功能仍不清楚。在本研究中,鉴定并表征了太平洋白虾(凡纳滨对虾)中编码RAS GTP酶(LvRac1)的cDNA。该GTP酶的重组变体rLvRac1在模式生物巴斯德毕赤酵母中表达,并通过质谱法确认了其表达。生化分析表明,重组蛋白保留了GTP酶活性,且在该生物体所有测试组织中均有表达。将溶藻弧菌注射到凡纳滨对虾体内可诱导肝胰腺中LvRac1表达上调。此外,体内敲低LvRac1可显著降低凡纳滨对虾p53和铜/锌超氧化物歧化酶基因(分别为Lvp53和LvCu/Zn SOD)的表达,同时增加半乳糖凝集素基因(Lvgal)的表达。通过流式细胞术分析对照和LvRac1沉默的凡纳滨对虾个体的血淋巴样本,发现后者的呼吸爆发活性和总血细胞计数显著降低。在溶藻弧菌攻击后,缺乏LvRac1的虾的累积死亡率显著高于对照组。因此,通过注射双链RNA沉默LvRac1可增加凡纳滨对虾对溶藻弧菌攻击的敏感性,并削弱其体内细菌清除能力。抑制LvRac1还促进了溶藻弧菌注射后Lvp53、LvCu/ZnSOD和Lvgal的上调。综上所述,这些结果表明LvRac1在凡纳滨对虾对溶藻弧菌感染的先天免疫反应中很重要。