Li Ming, Li Chaozheng, Ma Chunxia, Li Haoyang, Zuo Hongliang, Weng Shaoping, Chen Xiaohan, Zeng Digang, He Jianguo, Xu Xiaopeng
MOE Key Laboratory of Aquatic Product Safety/State Key Laboratory for Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, PR China; Guangxi Key Laboratory of Aquatic Genetic Breeding and Healthy Aquaculture, Guangxi Institute of Fisheries, Nanning, PR China.
MOE Key Laboratory of Aquatic Product Safety/State Key Laboratory for Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, PR China.
Dev Comp Immunol. 2014 Oct;46(2):231-40. doi: 10.1016/j.dci.2014.04.014. Epub 2014 May 1.
C-type lectins (CTLs) play crucial roles in innate immune responses in invertebrates by recognizing and eliminating microinvaders. In this study, a CTL from pacific white shrimp Litopenaeus vannamei (LvCTL3) was identified. LvCTL3 contains a single C-type lectin-like domain (CTLD), which shows similarities to those of other shrimp CTLs and has a mutated 'EPD' motif in Ca(2+)-binding site 2. LvCTL3 mRNA can be detected in all tested tissues and expression of LvCTL3 in gills was up-regulated after Lipopolysaccharides, poly (I:C), Vibrio parahaemolyticus and white spot syndrome virus (WSSV) challenges, suggesting activation responses of LvCTL3 to bacterial, virus and immune stimulant challenges. The 5'flanking regulatory region of LvCTL3 was cloned and we identified a NF-κB binding motif in the LvCTL3 promoter region. Dual-luciferase reporter assays indicated that over-expression of L. vannamei dorsal can dramatically up regulate the promoter activity of LvCTL3, suggesting that LvCTL3 expression could be regulated through NF-κB signaling pathway. As far as we know, this is the first report on signaling pathway involve in shrimp CTLs expression. The recombinant LvCTL3 protein was expressed in Escherichia coli and purified by Ni-affinity chromatography. The purified LvCTL3 can agglutinate Gram-negative microbe Vibrio alginolyticus and V. parahaemolyticus and Gram-positive bacteria Bacillus subtilis in the presence of calcium ions, but cannot agglutinate Gram-positive bacteria Streptococcus agalactiae. The agglutination activity of LvCTL3 was abolished when Ca(2+) was chelated with EDTA, suggesting the function of LvCTL3 is Ca(2+)-dependent. In vivo challenge experiments showed that the recombinant LvCTL3 protein can significantly reduce the mortalities of V. parahemolyticus and WSSV infection, indicating LvCTL3 might play significant roles in shrimp innate immunity defense against bacterial and viral infection.
C型凝集素(CTLs)通过识别和清除微小入侵者在无脊椎动物的先天免疫反应中发挥关键作用。在本研究中,鉴定出了来自凡纳滨对虾(Litopenaeus vannamei)的一种CTL(LvCTL3)。LvCTL3包含一个单一的C型凝集素样结构域(CTLD),它与其他对虾CTLs的结构域相似,并且在钙离子结合位点2处有一个突变的“EPD”基序。在所有测试组织中都能检测到LvCTL3 mRNA,并且在脂多糖、聚肌苷酸:聚胞苷酸、副溶血性弧菌和白斑综合征病毒(WSSV)刺激后,鳃中LvCTL3的表达上调,这表明LvCTL3对细菌、病毒和免疫刺激物刺激有激活反应。克隆了LvCTL3的5'侧翼调控区,并且我们在LvCTL3启动子区域鉴定出一个NF-κB结合基序。双荧光素酶报告基因分析表明,凡纳滨对虾背蛋白的过表达可显著上调LvCTL3的启动子活性,这表明LvCTL3的表达可能通过NF-κB信号通路进行调控。据我们所知,这是关于参与对虾CTLs表达的信号通路的首次报道。重组LvCTL3蛋白在大肠杆菌中表达并通过镍亲和层析纯化。纯化后的LvCTL3在钙离子存在的情况下能够凝集革兰氏阴性菌溶藻弧菌和副溶血性弧菌以及革兰氏阳性菌枯草芽孢杆菌,但不能凝集革兰氏阳性菌无乳链球菌。当钙离子与乙二胺四乙酸螯合时,LvCTL3的凝集活性被消除,这表明LvCTL3的功能是钙离子依赖性的。体内攻毒实验表明,重组LvCTL3蛋白可显著降低副溶血性弧菌和WSSV感染的死亡率,这表明LvCTL3可能在对虾先天免疫防御细菌和病毒感染中发挥重要作用。