Departament de Biologia Cellular, Fisiologia Animal i Immunologia, Universitat Autònoma de Barcelona, 08193 Cerdanyola, Catalunya, Barcelona, Spain.
Fish Shellfish Immunol. 2011 Jan;30(1):182-8. doi: 10.1016/j.fsi.2010.10.006. Epub 2010 Oct 15.
Gilthead seabream (Sparus aurata) and European seabass (Dicentrarchus labrax) were subjected to either experimental infection with Photobacterium damselae subsp. piscicida or Nodavirus after a period of 2 weeks of crowding in which fish were subjected to a 5-fold increase in density (10-50 kg/m(3)). Samples were obtained before the crowding period (0 h or control) and at 24h and 72 h after crowding from both groups of infected fish. The Complement haemolytic activity and the expression of the C3 gene were evaluated in blood and liver samples respectively. The bacteriolytic and lysozyme activities were also assessed. The results showed that Complement haemolytic activity was reduced at 72 h with both bacteria and virus in high density Gilthead seabream, and a similar increase was observed at low density. Bacteriolytic activity under both bacterial and viral challenges for both species was increased at 24h, under low density. At high density, the bacterial challenge did not induce significant changes. C3 mRNA abundance was substantially increased after pathogen treatments in low density groups at 24h but no significant changes were detected at high densities. These results support the idea of the suppressor effect of stressors on the immune system since a reduction of Complement activity under virus and high density, or lack of response in C3 expression under high density were observed.
在为期 2 周的拥挤期后,吉尔拉夫特真鲷(Sparus aurata)和欧洲鲈鱼(Dicentrarchus labrax)分别受到美人鱼发光杆菌亚种(Photobacterium damselae subsp. piscicida)或诺达病毒的实验感染,在此期间,鱼的密度增加了 5 倍(10-50 kg/m³)。在拥挤期之前(0 小时或对照)以及拥挤后 24 小时和 72 小时,从两组感染鱼中获得了样本。分别评估了血液和肝脏样本中的补体溶血活性和 C3 基因的表达。还评估了溶菌酶和溶菌酶活性。结果表明,在高密度真鲷中,两种细菌和病毒均在 72 小时降低了补体溶血活性,而在低密度时观察到类似的增加。在两种细菌和病毒的挑战下,两种鱼的溶菌酶活性在 24 小时时均在低密度下增加。在高密度下,细菌挑战未引起明显变化。在低密度组中,病原体处理后 C3 mRNA 丰度在 24 小时内大量增加,但在高密度下未检测到明显变化。这些结果支持了应激源对免疫系统的抑制作用的观点,因为在病毒和高密度下补体活性降低,或者在高密度下 C3 表达缺乏反应。