›› 2011, Vol. 38 ›› Issue (11): 113-116.

• 生物技术 • 上一篇    下一篇

快速检测双芽巴贝斯虫LAMP方法的建立

王素华1, 蔡渭明2, 李群3, 杜爱芳3   

  1. 1. 温州出入境检验检疫局,浙江温州 325027;2. 绍兴出入境检验检疫局,浙江绍兴 312000;3. 浙江大学动物预防医学研究所,浙江杭州 310029
  • 收稿日期:2011-04-06 修回日期:1900-01-01 出版日期:2011-11-20 发布日期:2011-11-20

Rapid Detection of Babesia bigemina by Loop-mediated Isothermal Amplification

WANG Su-hua1, CAI Wei-ming2, LI Qun3, DU Ai-fang3   

  1. 1. Wenzhou Entry-Exit inspection and Quarantine Bureau,Wenzhou 325027,China;2. Shaoxing Entry-Exit Inspection and Quarantine Bureau,Shaoxing 312000,China;3. Institute of Preventive Veterinary Medicine,Zhejiang University,Hangzhou 310029,China
  • Received:2011-04-06 Revised:1900-01-01 Online:2011-11-20 Published:2011-11-20

摘要: 为提高双芽巴贝斯虫(Babesia bigemina)检出率,本研究采用环介导等温扩增技术(LAMP)建立一种快速、灵敏、特异的B.bigemina检测方法。根据GenBank上公布的Babesia bigemina细胞色素b(Cytochrome b,cyt b)基因序列,设计4条特异地识别B.bigeminacyt b基因6个特殊区域的LAMP引物,优化反应体系和条件,在Bst DNA聚合酶的作用下,65 ℃反应60 min,加入SYBR Green Ⅰ后观察。结果表明,该LAMP检测方法特异性强,与牛巴贝斯虫(Babesia bovis)等DNA不发生交叉反应;敏感性高,对B.bigeminacyt b基因最小检测值为0.085 fg/μL,是一般PCR方法的1000倍。该方法具有简单、快速、低成本的特点,可用于B.bigemina的基层现场快速检测。

关键词: 双芽巴贝斯虫; 环介导等温扩增技术; 检测; cyt b基因

Abstract: A loop-mediated isothermal amplification(LAMP) assay for rapid detection of Babesia bigemina was developed using primers specific to six distinct regions of Cytochrome b gene of Babesia bigemina. LAMP was performed using Bst DNA polymerase at 65 ℃ in water bath for 60 min and amplification results was visualized with SYBR Green Ⅰ. Specific bands could be detected for Babesia bigemina,but not for others. The detection limit of the assay was 0.085 fg/μL for Babesia bigemina,which was up to 1000 times higher than that of PCR methods. The LAMP methods was rapid and could be easily performed at a low cost.

Key words: Babesia bigemina; loop-mediated isothermal amplification (LAMP); detection; cyt b gene

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