Aquatic Animal Health Research Unit, USDA-ARS, 990 Wire Road, Auburn, AL 36832, USA.
Fish Shellfish Immunol. 2013 Oct;35(4):1070-8. doi: 10.1016/j.fsi.2013.07.017. Epub 2013 Jul 25.
The objectives of this study were: 1) to determine the transcriptional profiles of G-protein coupled receptor 18 (GPR18) in channel catfish after infection with Aeromonas hydrophila compared to that in healthy catfish; 2) to determine whether over-expression of GPR18 in catfish gill cells will offer protection against infection of A. hydrophila; 3) to determine whether recombinant pcDNA-GPR18 could be used as an immunostimulant to protect channel catfish against A. hydrophila infection. Quantitative PCR revealed that the transcription levels of GPR18 in all tissues of infected catfish were significantly (P < 0.05) induced except in the intestine. When pcDNA3.2-vectored recombinant GPR18 was transfected in catfish gill cells G1B, the over-expression of pcDNA-GPR18 offered significant (P < 0.05) protection to G1B cells against A. hydrophila infection. When channel catfish were intraperitoneally injected with QCDCR adjuvant formulated pcDNA-GPR18 and challenged with a highly virulent A. hydrophila strain at 1-, 2-, 14-, and 28-days post treatment, pcDNA-GPR18 offered 50%, 100%, 57%, and 55% protection to channel catfish, respectively. Macrophages of fish treated with pcDNA-GPR18 produced significantly (P < 0.05) higher amounts of reactive oxygen species and nitric oxide than that of fish treated with pcDNA vector alone. In addition, serum lysozyme activity of catfish injected with pcDNA-GPR18 was significantly (P < 0.08) increased. Taken together, our results suggest that pcDNA-GPR18 could be used as a novel immunostimulant to provide immediate protection to channel catfish against A. hydrophila infection.
1)比较健康斑点叉尾鮰与感染嗜水气单胞菌后的斑点叉尾鮰中 G 蛋白偶联受体 18(GPR18)的转录谱,以确定 2)GPR18 在斑点叉尾鮰的鱼鳃细胞中的过表达是否可以提供对嗜水气单胞菌感染的保护,3)确定重组 pcDNA-GPR18 是否可以作为免疫刺激物来保护斑点叉尾鮰免受嗜水气单胞菌感染。实时定量 PCR 显示,除了肠道之外,所有感染鱼组织中的 GPR18 转录水平均显著(P < 0.05)诱导。当 pcDNA3.2 载体重组 GPR18 在斑点叉尾鮰的鱼鳃细胞 G1B 中转染时,pcDNA-GPR18 的过表达为 G1B 细胞提供了针对嗜水气单胞菌感染的显著(P < 0.05)保护。当斑点叉尾鮰被腹腔内注射 QCDCR 佐剂配方的 pcDNA-GPR18 并在治疗后 1、2、14 和 28 天用高毒力的嗜水气单胞菌菌株攻毒时,pcDNA-GPR18 分别为斑点叉尾鮰提供 50%、100%、57%和 55%的保护。用 pcDNA-GPR18 处理的鱼的巨噬细胞产生的活性氧和一氧化氮的量明显(P < 0.05)高于用 pcDNA 载体单独处理的鱼。此外,注射 pcDNA-GPR18 的斑点叉尾鮰的血清溶菌酶活性显著(P < 0.08)增加。综上所述,我们的结果表明,pcDNA-GPR18 可作为一种新型免疫刺激物,为斑点叉尾鮰提供针对嗜水气单胞菌感染的即时保护。