Chang Chin-Chyuan, Chang Hao-Che, Liu Kuan-Fu, Cheng Winton
Department of Aquaculture, National Pingtung University of Science and Technology, Pingtung 91201, Taiwan, ROC.
Tungkang Biotechnology Research Center, Fisheries Research Institute, C.O.A, Pingtung 92845, Taiwan, ROC.
Dev Comp Immunol. 2016 Jun;59:164-76. doi: 10.1016/j.dci.2016.02.003. Epub 2016 Feb 6.
Transglutaminases (TGs) play critical roles in blood coagulation, immune responses, and other biochemical functions, which undergo post-translational remodeling such as acetylation, phosphorylation and fatty acylation. Two types of TG have been identified in white shrimp, Litopenaeus vannamei, and further investigation on their potential function was conducted by gene silencing in the present study. Total haemocyte count (THC), differential haemocyte count (DHC), phenoloxidase activity, respiratory bursts (release of superoxide anion), superoxide dismutase activity, transglutaminase (TG) activity, haemolymph clotting time, and phagocytic activity and clearance efficiency to the pathogen Vibrio alginolyticus were measured when shrimps were individually injected with diethyl pyrocarbonate-water (DEPC-H2O) or TG dsRNAs. In addition, haemolymph glucose and lactate, and haemocytes crustin, lysozyme, crustacean hyperglycemic hormone (CHH), transglutaminaseI (TGI), transglutaminaseII (TGII) and clotting protein (CP) mRNA expression were determined in the dsRNA injected shrimp under hypothermal stress. Results showed that TG activity, phagocytic activity and clearance efficiency were significantly decreased, but THC, hyaline cells (HCs) and haemolymph clotting time were significantly increased in the shrimp which received LvTGI dsRNA and LvTGI + LvTGII dsRNA after 3 days. However, respiratory burst per haemocyte was significantly decreased in only LvTGI + LvTGII silenced shrimp. In hypothermal stress studies, elevation of haemolymph glucose and lactate was observed in all treated groups, and were advanced in LvTGI and LvTGI + LvTGII silenced shrimp following exposure to 22 °C. LvCHH mRNA expression was significantly up-regulated, but crustin and lysozyme mRNA expressions were significantly down-regulated in LvTGI and LvTGI + LvTGII silenced shrimp; moreover, LvTGII was significantly increased, but LvTGI was significantly decreased in LvTGI silenced shrimp following exposure to 28 and 22 °C. Knockdown of LvTGI and LvTGI + LvTGII also significantly increased the mortality of L. vannamei challenged with the pathogen V. alginolyticus. The same consequences have been confirmed in LvTGII silenced shrimp in our previous study. These results indicate that LvTGI and LvTGII not only reveal a complementary effect in gene expression levels but also play a key function in the immune defence mechanism of shrimp, by regulating the haemolymph coagulation, immune parameters and immune related gene expression, and in the regulation of carbohydrate metabolism.
转谷氨酰胺酶(TGs)在血液凝固、免疫反应及其他生化功能中发挥着关键作用,这些过程会经历如乙酰化、磷酸化和脂肪酰化等翻译后重塑。在凡纳滨对虾中已鉴定出两种类型的TG,本研究通过基因沉默对其潜在功能进行了进一步探究。当对虾分别注射焦碳酸二乙酯 - 水(DEPC - H₂O)或TG双链RNA(dsRNAs)后,测定了总血细胞计数(THC)、血细胞分类计数(DHC)、酚氧化酶活性、呼吸爆发(超氧阴离子释放)、超氧化物歧化酶活性、转谷氨酰胺酶(TG)活性、血淋巴凝固时间以及对溶藻弧菌病原体的吞噬活性和清除效率。此外,还测定了在低温胁迫下注射dsRNA的对虾的血淋巴葡萄糖和乳酸含量,以及血细胞中crustin、溶菌酶、甲壳动物高血糖激素(CHH)、转谷氨酰胺酶I(TGI)、转谷氨酰胺酶II(TGII)和凝血蛋白(CP)的mRNA表达。结果显示,在3天后接受凡纳滨对虾LvTGI dsRNA和LvTGI + LvTGII dsRNA的对虾中,TG活性、吞噬活性和清除效率显著降低,但THC、透明细胞(HCs)和血淋巴凝固时间显著增加。然而,仅在LvTGI + LvTGII沉默的对虾中,单个血细胞的呼吸爆发显著降低。在低温胁迫研究中,所有处理组的血淋巴葡萄糖和乳酸含量均升高,且在暴露于22°C后,LvTGI和LvTGI + LvTGII沉默的对虾中升高更为明显。在LvTGI和LvTGI + LvTGII沉默的对虾中,LvCHH mRNA表达显著上调,但crustin和溶菌酶mRNA表达显著下调;此外,在暴露于28°C和22°C后,LvTGI沉默的对虾中LvTGII显著增加,但LvTGI显著降低。敲低LvTGI和LvTGI + LvTGII也显著增加了受溶藻弧菌病原体攻击的凡纳滨对虾的死亡率。在我们之前的研究中,LvTGII沉默的对虾也证实了相同的结果。这些结果表明,LvTGI和LvTGII不仅在基因表达水平上表现出互补作用,而且通过调节血淋巴凝固、免疫参数和免疫相关基因表达以及碳水化合物代谢,在对虾的免疫防御机制中发挥关键作用。