欧洲鳗鲡膨化颗粒饲料养殖试验

本实验用“海马”牌幼鳗膨化颗粒饲料和幼鳗粉状饲料进行了为期４９ｄ的欧洲鳗鲡养殖对比试验,结果表明,膨化颗粒饲料具有良好的适口性和较高的饲料效率（７０．８％）,可保证鳗于的正常摄食和生长,并能降低养殖用饲料成本,减轻对水质的污染,提高鳗鱼生长的均匀度。     

鳗鲡气单胞菌引起的烂尾病病原菌抑菌药物的研究

应用药敏纸片法研究了三株烂尾病病原菌（气单胞菌）对３１种药物及不同配合药物的敏感性，测定了４种药物及配合药物ＨＰ对三株菌的最低抑菌浓度（ＭＩＣ）及最低杀菌浓度（ＭＢＣ）。结果表明，配合药物ＨＰ具较强的抑菌能力。     

欧洲鳗鲡胃肠道激素免疫组织化学的研究

用免疫组织化学技术研究了9种哺乳动物胃肠道激素抗体在正常生长欧鳗和僵鳗胃肠道的定位分布,研究结果表明,5－HT,SOM,GAS,α－1－AT和P物质免疫活性内分泌细胞存在于正常鳗和僵鳗胃肠道中,其余4种抗体显阴性反应,文中讨论了胃肠道激素在僵鳗成因中可能的生理作用。     

欧洲鳗鲡的性分化和僵鳗成因的探讨

欧洲鳗鲡性分化时间在白仔鳗转变为黑仔鳗时期体长１０．５－１２．０ｃｍ,性腺切片观察可见雌性卵巢中有原始卵原细胞雄性生精小管中有精原细胞,性别分化明显旱鳗鲡从福建省两个养鳗场采集僵鳗,取甚生腺切片观察有精原除个别僵鳗外,全部为雄性,提示僵鳗成因可能与性别有关。文中讨论了发生僵鳗的复杂因素。     

欧洲鳗鲡肝肾病病原菌的分离与鉴定

患肝肾病的养殖欧洲鳗鲡(Anguilla anguilla)出现肝、肾肿大,且肝脏具白色溃疡灶的症状。从肝脏中分离、纯化到优势细菌,定名AL60306NA1。人工感染试验证实:向欧洲鳗鲡腹腔内注射1.0×108cfu/mL菌株悬液,实验鱼死亡率达100.0%;注射1.0×107cfu/mL,死亡率为60.0%;形态学观察、API20E细菌鉴定试剂盒鉴定实验证明菌株AL60306NA1有动力、拥有革兰氏反应阴性、氧化酶阴性、H2O2酶阳性、兼性厌氧、发酵葡萄糖产酸产气、不发酵蔗糖和蜜二糖及L一阿拉伯糖、赖氨酸脱羧酶阳性、柠檬酸盐弱阳性、产生硫化氢和吲哚、MR阳性和典型的β-溶血等特征;16S rRNA特异性基因分析鉴定实验说明克隆的AL60306NA1 16S rRNA基因部份序列为1507bp、与迟缓爱德华氏菌(AB050829.1)的同源性达99.7%。综合上述结果,确定该菌株为养殖欧洲鳗鲡肝肾病的病原菌,并鉴定为迟缓爱德华氏菌(Edwardsiella tarda)野生型。用菌株AL60306NA1感染小白鼠实验测定该菌对小白鼠的LD50为7.1×105cfu/mL,同时自该菌株PCR扩增到长度约1000bp的溶血素基因特异性片段,结果表明菌株AL60306NA1有一定的致病力。     

福建省养殖鳗鲡细菌性疾病的调查与防治

自１９９３年１１月－１９９５年６月，对福建省养殖鳗鲡的细菌性疾病进行了调查，共调查到８种细菌病，本文介绍各种细菌病的流行病学。诊断方法及防治措施。     

海水养殖尼罗罗非鱼尾鳍腐烂病的病原菌性状

对海水养殖尼罗罗非鱼Oreochromis niloticus尾鳍腐烂病(烂尾病)病原菌的形态、生理生化特性进行了研究。经鉴定为嗜水气单胞菌无气亚种Aeromonas hydrophila subsp.anaero-genes Schubert.菌体细胞为直杆,单个,以单极鞭毛运动,革兰氏染色阴性。患病鱼行动迟缓,常浮在水面上游动,鱼体变黑至死亡。     

日本鳗鲡(Anguilla japonica)和欧洲鳗鲡(A. anguilla)的微卫星差异

采用PCR扩增单位点微卫星的方法研究了日本鳗鲡(Anguilla japonica)和欧洲鳗鲡(A. anguilla)的遗传差异.结果表明,微卫星等位基因数目分布范围为8-26,35组被试(5个分类单元各7个位点)的显著性检验的结果表明其杂合性显著缺乏(P＜0.01),日本鳗鲡的4个亚种群的所有微卫星位点均偏离哈-温平衡,对日本鳗鲡种群分化进行的正合检验结果也否定了种内个体随机分布的假设.FST值为0.0098(P=0.00048)揭示了日本鳗鲡亚种群内存在较弱但显著的遗传分化.各分类单元间的FST及RST逐一对应矩阵显示了日本鳗鲡与欧洲鳗鲡两个远缘种之间存在显著差异.计算Goldstein的遗传距离并由此推算出两个种的分化时间约为200多万年.     

欧鳗“狂游症”病毒的细胞定位与超微病变

应用电镜标本制备和观察技术对45尾“狂游症”欧鳗的主要脏器进行系统观察，在脑、心脏、肌肉和皮肤组织中，发现一种致病性病毒，多数病毒定位于细胞的内质网腔，一般为球状或椭圆球状，大小约为50～80nm×100～150nm，具有囊膜，囊膜外附有纤突，可以造成脑细胞的肿胀、空泡变性和心肌细胞线粒体的结构破坏和空泡化等细胞病变．人工感染欧鳗中找到同样病毒，表明该病毒是欧鳗“狂游症”的致病原．     

BSA-ISCOMs对欧洲鳗鲡免疫效应及抗细菌性病原的效果研究

为证实免疫刺激复合物(ISCOMs)的非特异免疫增强作用,将牛血清白蛋白(BSA)制备成ISCOMs(BSA-ISCOMs).将欧洲鳗鲡(Anguilla anguilla)随机分为3组,分别用BSA-ISCOMs、BSA和磷酸盐缓冲液(PBS,对照组)腹腔注射免疫.二次免疫完成后第30d采血,测血清部分非特异性免疫指标,剩余鳗鲡分别用创伤弧菌(Vibrio vulnificus)和嗜水气单胞菌(Aeromona hydrophila)攻毒.结果显示,BSA-ISCOMs组的血清溶菌酶活力显著高于BSA组和对照组(p≤0.05);超氧化物歧化酶(SOD)和补体C3活力与对照组无显著差异(p0.05).攻毒结果显示,BSA-ISCOMs组的存活率显著高于BSA组和对照组(p≤0.05),对创伤弧菌和嗜水气单胞菌攻击的相对免疫保护率分别为43.3%和51.7%.表明BSA-ISCOMs能有效增强欧洲鳗鲡对主要病原创伤弧菌和嗜水气单胞菌的抗病能力.     

欧洲鳗病原菌控菌药物的研究

应用药敏纸片法测定２４种抗菌药物对欧洲鳗致病菌：非０１群霍乱弧菌、温和气单胞菌、鲁氏不动杆菌、迟钝爱德华氏菌和嗜水气单胞菌的敏感性。其中,诺氟沙星、四环素、头孢三嗪、庆大霉素、头孢噻肟抑菌能力较强。最低抑菌浓度（ＭＩＣ）和最低杀菌浓度（ＭＢＣ）测定结果表明孢三嗪对病原菌能力强。最低抑菌浓度（ＭＩＣ）和最低杀菌浓度（ＭＢＣ）测定结果表明,头孢三嗪对病原菌杀灭能力强,复方新诺明、硫酸庆大霉素对病原菌抑     

Induction of DNA strand breakage and apoptosis in the eel Anguilla anguilla

The ability of benzo[a]pyrene, Aroclor 1254, 2-3-7-8-tetrachlorodibenzo-p-dioxin and beta-naphthoflavone to induce DNA strand breaks (SB) and apoptosis in erythrocytes of the European eel (Anguilla anguilla) was investigated following by in vivo exposure. DNA damage was evaluated by the Comet assay, while the diffusion assay was used to investigate the induction of apoptosis 7 days after a single intraperitoneal administration. 2-3-7-8-Tetrachlorodibenzo-p-dioxin induced the highest genotoxic effect, followed by benzo[a]pyrene, while the other two substances had limited effects. A significant induction of apoptosis was observed at the highest doses after exposure to benzo[a]pyrene, when DNA damage was also elevated. The occurrence of apoptotic cells after exposure to Aroclor, 2-3-7-8-tetrachlorodibenzo-p-dioxin and beta-naphthoflavone was quite variable and did not show clear dose-related responses. The role of oxidative stress in mediating DNA damage was also discussed.     

Evidence of marine mammal predation of the European eel (Anguilla anguilla L.) on its marine migration

Temperature and depth logging tags were implanted into adult eels released on Atlantic west coasts of France and Ireland to study their oceanic migration behavior. For three of the tags, 25 to 256 days after release there was a dramatic rise in temperature from 10 °C to 36 °C and the dive profile changed from depths of 300–1000 m to repeated ascents to the surface. This indicated that the eels carrying the tags had been eaten by a mammalian predator. Two of the tags had sufficient sampling rate to resolve the dives in detail. They recorded a total of 91 dives to maximum depths of 250–860 m lasting 11–12 min and with surface intervals of 5–7 min. More than two thirds of the dives included a rapid descent from approximately 500 m to 600–700 m. From this we infer that the predator was most likely a deep-diving toothed whale. The dives logged while the tags were inside the predator revealed that the temperature usually decreased during dives, and increased again during surface periods. The temperature drops during dives were probably caused by the ingestion of prey or water. These observations provide insights into the behavior of toothed whales foraging in the mesopelagic zone.