首页 | 期刊介绍 | 编委会 | 道德声明 | 投稿指南 | 常用下载 | 过刊浏览 | In English
引用本文:李杰,莫照兰,茅云翔,肖鹏.两株养殖大菱鲆体表出血病原菌的分离鉴定[J].海洋科学,2008,32(10):1-5.
【打印本页】   【HTML】   【下载PDF全文】   查看/发表评论  下载PDF阅读器  关闭
←前一篇|后一篇→ 过刊浏览    高级检索
本文已被:浏览 1798次   下载 1754 本文二维码信息
码上扫一扫!
分享到: 微信 更多
两株养殖大菱鲆体表出血病原菌的分离鉴定
李杰1, 莫照兰2, 茅云翔3, 肖鹏2
1.中国海洋大学水产学院;2.中国科学院海洋研究所海洋生物学开放实验室;3.中国海洋大学海洋生命学院
摘要:
从秦皇岛和胶南患出血病的大菱鲆(Scophthalmus maximus)肾脏中分别分离得到优势菌株MHK2和JN,人工感染实验证实这两株菌对大菱鲆有较强的致病性,半数致死量(LD50)分别为6.30×103cfu/尾和2.51×104cfu/尾。对病原菌16s rDNA序列对比分析及进化树分析表明,MHK2和JN与迟缓爱德华氏菌(Edwardsiella tarda)高度一致。API ID32E快速鉴定结果表明,MHK2和JN生理生化特征与非致病性迟缓爱德华氏菌标准菌株LSE6一致,属于迟缓爱德华氏菌。经API ZYM酶活检测,MHK2和JN的碱性磷酸盐酶和酸性磷酸酶活性明显高于LSE6,这两项酶活特征有望作为区别致病性和非致病性迟缓爱德华氏菌的一个标准。
关键词:  大菱鲆(Scophthalmus maximus)  出血病  迟缓爱德华氏菌(Edwardsiella tarda)
DOI:
分类号:
基金项目:国家高技术研究发展计划项目(2006AA100310);;国家重点基础研究发展计划资助项目(2006CB101803);;国家海洋局908专项项目(908-01-ZH3);;国家自然科学基金资助项目(30671613)
Isolation and classification of two pathogenic bacteria associated with hamorrhages of Scophthalmus maximus
Abstract:
Two dominated strains MHK2 and JN were isolated from cultured turbot (Scophthalmus maximus) with hamorrhage disease in Qinhuangdao and Jiaonan respectively. Infection experiments showed that two strains were highly pathogenic to turbot. The LD50 of MHK2 is 6.30×103 cfu/fish, and JN is 2.51×104 cfu/fish. The sequences of 16S rDNA of MHK2 and JN were compared to those in Genbank Datebase. They shared high similarity to Edwardsiella tarda. By API ID32E systematic identification,MHK2 and JN were similar in characteristics to E. tarda standard strain LSE6, and were indentified as E. tarda. By API ZYM enzymatic activity detection, MHK2 and JN were significantly higher in alkaline phosphatase and acid phosphatase activity than those of LSE6. These two charcteristics may be a way to distinguish the pathoge nicity from the non-pathogenic E. tarda.
Key words:  Scophthalmus maximus  Hamorrhages  Edwardsiella tarda
版权所有 《海洋科学》 Copyright©2008 All Rights Reserved
主管单位:中国科学院 主办单位:中国科学院海洋研究所
地址:青岛市市南区福山路32号  邮编:266071  电话:0532-82898755  E-mail:marinesciences@qdio.ac.cn
技术支持:北京勤云科技发展有限公司