Dipartimento di Scienze Ambientali, Largo dell'Università, Università degli Studi della Tuscia, Viterbo 01100, Italy.
Fish Shellfish Immunol. 2010 Feb;28(2):303-11. doi: 10.1016/j.fsi.2009.11.008. Epub 2009 Nov 17.
Naïve sea bass juveniles (38.4 + or - 4.5 g) were intramuscularly infected with a sublethal dose of betanodavirus isolate 378/I03, followed after 43 days by a similar boosting. This infection resulted in an overall mortality of 7.6%. At various intervals, sampling of fish tissues was performed to investigate: i) B and T lymphocyte content in organs and tissues; ii), proliferation of leucocytes re-stimulated in vitro with inactivated virus; iii) presence of serum antibody specific for betanodavirus; iv) expression of genes coding for the following immunoregulatory molecules involved in innate and acquired responses: type I IFN, Mx, IL-1, Cox-2; IL-10, TGF-beta, TCRbeta, CD4, CD8alpha, IgM, by using a quantitative PCR array system developed for sea bass. The obtained results showed a detectable increase of T cells and B cells in PBL during betanodavirus infection. Furthermore, leucocytes obtained from blood, head kidney, and gills showed a detectable "in vitro" increase in viability upon addition of inactivated viral particles, as determined by measuring intracellular ATP concentration. ELISA analysis of sera showed that exposure to nodavirus induced a low, but specific antibody titer measured 43 days after infection, despite the presence of measurable levels of natural antibody. Finally, a strong upregulation of genes coding for type I IFN, Mx, and IgM was identified after both infection and boosting. Interestingly, an upregulation of Cox-2 until boosting, and of TGF-beta and IL-10 after boosting was also observed, while the other tested genes did not show any significant variations with respect to mock-treated fish. Overall, our work represents a first comprehensive analysis of cellular and molecular immune parameters in a fish species exposed to a pathogenic virus.
未成熟的海鲈幼鱼(38.4 ± 4.5 g)肌肉内感染了贝塔诺病毒分离株 378/I03 的亚致死剂量,43 天后再次进行类似的加强感染。这导致了 7.6%的总死亡率。在不同的时间间隔内,对鱼类组织进行采样,以研究:i)器官和组织中 B 和 T 淋巴细胞的含量;ii)体外用灭活病毒刺激后的白细胞增殖;iii)针对贝塔诺病毒的特异性血清抗体的存在;iv)编码参与先天和获得性反应的以下免疫调节分子的基因的表达:I 型 IFN、Mx、IL-1、Cox-2;IL-10、TGF-β、TCRβ、CD4、CD8α、IgM,使用为海鲈开发的定量 PCR 阵列系统。获得的结果表明,在贝塔诺病毒感染期间,PBL 中可检测到 T 细胞和 B 细胞的增加。此外,从血液、头肾和鳃中获得的白细胞在加入灭活病毒颗粒后,通过测量细胞内 ATP 浓度,显示出可检测的“体外”活力增加。ELISA 分析血清表明,尽管存在可测量水平的天然抗体,但暴露于诺达病毒会诱导低但特异性的抗体滴度,在感染后 43 天测量。最后,在感染和加强感染后,鉴定出编码 I 型 IFN、Mx 和 IgM 的基因的强烈上调。有趣的是,在加强感染后还观察到 Cox-2 的上调,以及 TGF-β 和 IL-10 的上调,而其他测试的基因与模拟处理的鱼类相比没有显示出任何显著变化。总的来说,我们的工作代表了对一种鱼类暴露于致病性病毒后的细胞和分子免疫参数的首次全面分析。