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驽巴贝斯虫病PCR检测方法的建立和应用

罗金 刘光远 谢俊仁 田占成 沈辉 王芳芳 孙晓林 陈荣贵 王海军

中国畜牧兽医2011,Vol.38Issue(7):193-195,3.
中国畜牧兽医2011,Vol.38Issue(7):193-195,3.

驽巴贝斯虫病PCR检测方法的建立和应用

Application and Development of PCR Assay to Detect Babesia caballi

罗金 1刘光远 2谢俊仁 3田占成 3沈辉 3王芳芳 3孙晓林 3陈荣贵 1王海军4

作者信息

  • 1. 甘肃农业大学动物医学院,甘肃兰州730070
  • 2. 中国农业科学院兰州兽医研究所家畜疫病病原生物学 国家重点实验室甘肃省动物寄生虫病重点实验室农业部草食动物疫病重点开放实验室,甘肃兰州 730046
  • 3. 中国农业科学院兰州兽医研究所家畜疫病病原生物学 国家重点实验室甘肃省动物寄生虫病重点实验室农业部草食动物疫病重点开放实验室,甘肃兰州 730046
  • 4. 新疆伊犁州动物疾病控制与诊断中心,新疆伊犁735000
  • 折叠

摘要

Abstract

The 18S rRNA gene recently discovered was shown to be species-specific. A pair of primers was designed to specifically amplified a 452 bp fragment. The PCR result of specificity assay showed that one references B. Caballi could be detected by the PCR test,but no amplification was observed when other five bacterial species isolated from T. Equi,B. Bigimina,B. Motasi, B. Ovata, B. Major tissue were detected. And the sensitivity result showed that the minimum dose of B. Caballi that could be detected by PCR assay was 0. 01 fg/μL,45 clinical sample, from horses farm in China, doubtedly infected with B. Caballi were tested by PCR. The results showed that 12 positive samples could be detected by the PCR assay. At the same time,microscope were also used for the clinical samples. The test revealed that the sensitivity of the PCR assay was higher than that the microscope test.

关键词

驽巴贝斯虫/PCR诊断方法/应用

Key words

Babesia caballi /PCR diagnosis method /application

分类

农业科技

引用本文复制引用

罗金,刘光远,谢俊仁,田占成,沈辉,王芳芳,孙晓林,陈荣贵,王海军..驽巴贝斯虫病PCR检测方法的建立和应用[J].中国畜牧兽医,2011,38(7):193-195,3.

基金项目

甘肃省科技重大专项(092NKDA031). (092NKDA031)

中国畜牧兽医

OA北大核心CSTPCD

1671-7236

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