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建立环介导等温扩增方法快速检测鱼类链球菌病病原体鳗孤菌。

Development of loop-mediated isothermal amplification method for rapid detection of Streptococcus iniae, the causative agent of streptococcicosis in fish.

机构信息

Fisheries College, Guangdong Ocean University, Zhanjiang, China.

出版信息

J Basic Microbiol. 2012 Apr;52(2):116-22. doi: 10.1002/jobm.201100082. Epub 2011 Jul 21.

Abstract

Streptococcus iniae is a major pathogen that causes sever economic losses in tilapia aquaculture. A set of four specific primers was designed by targeting lctO gene. With Bst DNA polymerase, the target DNA can be clearly amplified for 60 min at 64 °C in a simple water bath. The sensitivity of the LAMP assay for the detection of S. iniae is about 12.4 cells per reaction in both of pure cultures and added fish tissues cultures. LAMP products could be judged with agar gel or naked eye after addition of SYBR Green I. There were no cross-reactions with other bacterial strains indicating high specificity of the LAMP. The LAMP method was also applied to detect S. iniae-infected tilapia tissues effectively. The LAMP assay reported here indicates the potential usefulness of the technique as a valuable simple, rapid alternative procedure for the detection of S. iniae during streptococcicosis monitoring of cultured fish.

摘要

杀鲑气单胞菌是一种主要的病原体,可导致罗非鱼养殖业遭受严重的经济损失。本研究针对 lctO 基因设计了四组特异性引物,使用 Bst DNA 聚合酶在简单的水浴中于 64°C 下即可将目标 DNA 清晰地扩增 60 分钟。LAMP 检测法对纯培养物和添加的鱼组织培养物中 S. iniae 的检测灵敏度约为每个反应 12.4 个细胞。加入 SYBR Green I 后,可通过琼脂凝胶或肉眼判断 LAMP 产物。与其他细菌菌株无交叉反应,表明该方法具有高度特异性。该 LAMP 方法还可有效用于检测感染杀鲑气单胞菌的罗非鱼组织。本研究报告的 LAMP 检测法表明,该技术具有作为一种简单、快速的替代方法,在养殖鱼类链球菌病监测中用于检测 S. iniae 的潜在用途。

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