Grove Søren, Johansen Renate, Reitan Liv J, Press Charles M, Dannevig Birgit H
Department of Immunoprophylaxix, National Veterinary Institute, PO Box 8156 Dep., 0033 Oslo, Norway.
Fish Shellfish Immunol. 2006 Nov;21(5):525-39. doi: 10.1016/j.fsi.2006.03.001. Epub 2006 Mar 22.
The present study reports the quantitative analysis of the spatio-temporal development of nodavirus infection and corresponding immune response in juvenile Atlantic halibut (Hippoglossus hippoglossus) challenged by intramuscular injection of nodavirus. Novel quantitative real-time RT-PCR protocols were applied to evaluate the absolute copy numbers of nodavirus RNA2 (RNA2) and secretory-IgM mRNA (sec-igmicro) in the eye, brain, mid/posterior kidney and spleen sampled over a period of 81 days. In the eye and brain, levels of both RNA2 and sec-igmicro increased significantly early in the infection. In the spleen and mid/posterior kidney, both RNA2 and sec-igmicro were detected but the levels remained unchanged during the experimental period. The levels of RNA2 and sec-igmicro in the eye and brain were strongly correlated (P<0.0001). Nodavirus antigen was demonstrated by immunohistochemistry (IHC) in the retina of eyes from a relatively few fish from day 34 post challenge (brain not examined), but not at any time in the spleen and anterior kidney. By IHC, IgM+ cells were observed in conjunction with nodavirus positive IHC labelling in the retina. In both the spleen and anterior kidney, the number of IgM+ cells increased from day 3 post challenge. By conventional real-time RT-PCR, RNA2 was only sporadically demonstrated in the posterior intestine, heart and gills. ELISA analysis revealed a nodavirus specific antibody response in serum that was significant from day 18 post challenge. No clinical signs or mortality related to nodavirus infection were observed in the challenged halibut. The results suggest that the nodavirus infection induced a significant antibody response through activation of B-cells in the kidney and spleen, and involved a substantial migration of antibody-secreting cells to infected peripheral tissues.
本研究报告了通过肌肉注射诺达病毒对幼年大西洋庸鲽(Hippoglossus hippoglossus)进行攻击后,诺达病毒感染的时空发展及相应免疫反应的定量分析。应用新型定量实时逆转录聚合酶链反应(RT-PCR)方案,评估在81天内采集的眼、脑、中/后肾和脾脏中诺达病毒RNA2(RNA2)和分泌型免疫球蛋白M mRNA(sec-igmicro)的绝对拷贝数。在眼和脑中,RNA2和sec-igmicro的水平在感染早期均显著升高。在脾脏和中/后肾中,检测到了RNA2和sec-igmicro,但在实验期间其水平保持不变。眼和脑中RNA2和sec-igmicro的水平呈强相关(P<0.0001)。通过免疫组织化学(IHC)在攻毒后34天起在相对较少的鱼的眼中视网膜中检测到诺达病毒抗原(未检查脑),但在脾脏和前肾中任何时候均未检测到。通过IHC,在视网膜中观察到IgM+细胞与诺达病毒阳性IHC标记同时出现。在脾脏和前肾中,IgM+细胞的数量从攻毒后第3天开始增加。通过传统实时RT-PCR,仅在后肠、心脏和鳃中偶尔检测到RNA2。酶联免疫吸附测定(ELISA)分析显示,血清中诺达病毒特异性抗体反应从攻毒后第18天起显著。在受攻击的庸鲽中未观察到与诺达病毒感染相关的临床症状或死亡。结果表明,诺达病毒感染通过激活肾和脾中的B细胞诱导了显著的抗体反应,并涉及抗体分泌细胞大量迁移至受感染的外周组织。