Bakopoulos V, Hanif A, Poulos K, Galeotti M, Adams A, Dimitriadis G J
Division of Genetics, Department of Biology, University of Patras, Greece.
J Fish Dis. 2004 Jan;27(1):1-13. doi: 10.1046/j.1365-2761.2003.00513.x.
Photobacterium damsela subsp. piscicida, the causative agent of fish pasteurellosis, was grown in vivo. Bacterial cells and extracellular products (ECPs) were analysed via electrophoresis and immunoblot analysis, using specific sea bass antisera. Growth in vivo induced the synthesis of unique bacterial cell proteins at > 206, 206, 21.3, 18, 7.6 and < 7.6 kDa. Sea bass serum raised against live bacterial cells of the pathogen and especially a sea bass serum raised against formalin-inactivated bacterial cells grown in a specific novel medium recognized the novel antigens at > 206 (associated with iron sequestration), 21.3, 7.6 and < 7.6 kDa, suggesting that the latter medium conserves the synthesis of natural bacterial cell proteins in vitro. In vivo growth of the pathogen induced the synthesis of more toxic ECPs in comparison with in vitro growth and an inverse correlation between total protein concentration in the ECPs and toxicity per unit of protein was observed. Substrate-polyacrylamide electrophoresis revealed the presence of in vivo synthesized ECPs of the pathogen (proteases) at 175, 132, < 79 and 48.3 kDa. Histological examination of tissues isolated from fish injected with these ECPs revealed inflammatory and necrotic lesions in the spleen, liver, head kidney, intestine and heart as soon as 48 h post-introduction of the ECPs.
杀鲑气单胞菌嗜鱼亚种是鱼类巴斯德氏菌病的病原体,在体内进行培养。使用特异性海鲈抗血清,通过电泳和免疫印迹分析对细菌细胞和细胞外产物(ECPs)进行分析。体内生长诱导合成了分子量大于206、206、21.3、18、7.6和小于7.6 kDa的独特细菌细胞蛋白。针对病原体活细菌细胞产生的海鲈血清,尤其是针对在特定新型培养基中生长的福尔马林灭活细菌细胞产生的海鲈血清,识别出分子量大于206(与铁螯合相关)、21.3、7.6和小于7.6 kDa的新型抗原,这表明后一种培养基在体外保留了天然细菌细胞蛋白的合成。与体外生长相比,病原体的体内生长诱导合成了毒性更强的ECPs,并且观察到ECPs中总蛋白浓度与每单位蛋白毒性之间呈负相关。底物 - 聚丙烯酰胺电泳显示,病原体(蛋白酶)在体内合成的ECPs分子量为175、132、小于79和48.3 kDa。对注射这些ECPs的鱼所分离组织进行的组织学检查显示,在引入ECPs后48小时,脾脏、肝脏、头肾、肠道和心脏就出现了炎症和坏死性病变。