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作 者:朱壮春[1] 陈阳[1] 郝东升[2] 马玉妹[1] 王艳茹[1] 曹向可[1] 穆艮艮[1] 李金坤[1] 史相国
机构地区:[1]华北煤炭医学院生物科学系,河北唐山063000 [2]华北煤炭医学院附属医院,河北唐山063000 [3]陡河水库管理处,河北唐山063000
出 处:《水产科学》2010年第6期363-365,共3页Fisheries Science
基 金:唐山市科技局科技攻关项目(06125401A-3)
摘 要:用迟钝爱德华氏菌免疫家兔,制备出高效价迟钝爱德华氏菌免疫血清。先制备迟钝爱德华氏菌抗原,耳缘静脉注射免疫家兔。经微量反应板法检测血清效价,效价达到1∶2560;用Millipore Montage抗体纯化试剂纯化抗体,纯化的抗体经SDS-PAGE电泳,杂带较少,条带主要集中于50 kD处;用斑点酶联免疫吸附试验检测时,迟钝爱德华氏菌呈阳性,温和气单胞菌、嗜水气单胞菌、河流弧菌、溶藻弧菌、鳗弧菌、腐败希瓦氏菌、产碱普罗威斯登菌、阪崎肠杆菌和大肠杆菌均呈阴性。试验结果表明,特异、高效价的迟钝爱德华氏菌免疫血清,为快速检测牙鲆腹水病病原奠定了基础。The methods used in preparation of high-titer anti-Edwardsieua tarda(Et) serum by immunized rabbits with E.trada were described as the following:Firstly,the antigen of Et was prepared by the rabbits vaccinated by an ear vein.The agglutination efficiency of the immune serum was found to be 1︰2560 with micro-reaction plate.Then,the antibody was purified by Millipore Montage antibody purified kit,and the purified antibodies by SDS-PAGE electrophoresis with less miscellaneous focus had the main strip of about 50 kD.E.tarda was positive in the Dot-ELISA while Aeromonas sobria,A.hydrophila,Vibrio fluvialis,V.alginolyticus,V.anguillarum,Shewanella putrefaciens,Providencia alcalifaciens,Enterobacter sakazakii and Escherichia coli were negative in the assay.The specificity and high titer of immune serum were produced in this study,leading to a strategy to detect Bifidobacteriumin dairy products serologically.The specificity and high titer E.tarda immune serum provide the foundation for the rapid detection of pathogenic bacteria in Japanese flounder(Paralichthys olivaceus)with ascites.
关 键 词:牙鲆 迟钝爱德华氏菌 免疫血清 纯化 斑点酶联免疫吸附试验
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