LaFrentz Benjamin R, LaPatra Scott E, Jones Gerald R, Cain Kenneth D
Department of Fish and Wildlife Resources, Aquaculture Research Institute, University of Idaho, Moscow, Idaho 83844-1136, USA.
Dis Aquat Organ. 2004 Apr 21;59(1):17-26. doi: 10.3354/dao059017.
Vaccine development for coldwater disease (CWD), also known as rainbow trout fry syndrome (RTFS), has been based primarily on whole-cell bacterins or outer membrane fractions of Flavobacterium psychrophilum. In the present study, immunogenic regions of the bacterium corresponding to 18-28, 41-49, and 70-100 kDa were identified by western blot analysis using rainbow trout Oncorhynchus mykiss immune sera. Following sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), antigens within these regions were isolated by electro-elution and used in immunization trials. Groups of rainbow trout fry were immunized with these regions emulsified with Freund's complete adjuvant (FCA) and a formalin-killed bacterin emulsified with FCA. It was demonstrated that the 70-100 and 41-49 kDa regions and F. psychrophilum treatments elicited significant protection when compared to the saline control following subcutaneous challenge with 2 doses of a virulent strain of F. psychrophilum. Immunization with the 70-100 kDa region resulted in near complete protection in fish with mean cumulative percent mortality (CPM) of 6% and mean relative percent survival (RPS) of 94% at the lower challenge dose (6.25 x 10(6) colony forming units fish(-1)). This preparation also stimulated a high level of specific antibody to F. psychrophilum, as detected by an enzyme-linked immunosorbent assay (ELISA). Western blot analysis using sera from fish immunized with the 70-100 kDa region demonstrated that high molecular weight proteins and the O-polysaccharide component of lipopolysaccharide (LPS) are recognized by serum antibodies. This suggests that these antigens may be involved in eliciting a highly protective immune response, and could serve as vaccine candidates.
冷水病(CWD),也称为虹鳟鱼苗综合征(RTFS),其疫苗研发主要基于嗜冷黄杆菌的全细胞菌苗或外膜组分。在本研究中,使用虹鳟Oncorhynchus mykiss免疫血清通过蛋白质免疫印迹分析确定了该细菌对应于18 - 28 kDa、41 - 49 kDa和70 - 100 kDa的免疫原性区域。在十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE)后,通过电洗脱分离这些区域内的抗原,并用于免疫试验。将虹鳟鱼苗分组,用这些区域与弗氏完全佐剂(FCA)乳化后的制剂以及用FCA乳化的福尔马林灭活菌苗进行免疫。结果表明,与用盐水对照相比,在用两剂嗜冷黄杆菌强毒株进行皮下攻击后,70 - 100 kDa和41 - 49 kDa区域以及嗜冷黄杆菌处理均引发了显著的保护作用。用70 - 100 kDa区域进行免疫,在较低攻击剂量(6.25×10⁶菌落形成单位/鱼⁻¹)时,鱼的平均累积死亡率(CPM)为6%,平均相对存活率(RPS)为94%,几乎实现了完全保护。通过酶联免疫吸附测定(ELISA)检测,该制剂还刺激产生了高水平的针对嗜冷黄杆菌的特异性抗体。使用来自用70 - 100 kDa区域免疫的鱼的血清进行蛋白质免疫印迹分析表明,血清抗体可识别高分子量蛋白质和脂多糖(LPS)的O - 多糖组分。这表明这些抗原可能参与引发高度保护性免疫反应,并可作为候选疫苗。