牛支原体、无乳支原体和丝状支原体丝状亚种小克隆三重PCR检测方法的建立及初步应用

合集下载
  1. 1、下载文档前请自行甄别文档内容的完整性,平台不提供额外的编辑、内容补充、找答案等附加服务。
  2. 2、"仅部分预览"的文档,不可在线预览部分如存在完整性等问题,可反馈申请退款(可完整预览的文档不适用该条件!)。
  3. 3、如文档侵犯您的权益,请联系客服反馈,我们会尽快为您处理(人工客服工作时间:9:00-18:30)。

牛支原体、无乳支原体和丝状支原体丝状亚种小克隆三重
PCR检测方法的建立及初步应用
李大伟;黄灿平;张彦明;谢建华;冉智光;熊仲良;范伟兴
【期刊名称】《畜牧兽医学报》
【年(卷),期】2011(042)002
【摘要】The study was aimed at establishing a triplex PCR to differentiate M. bovis, M. mycoides subsp. mycoides Small Colony Type and M. agalactiae out of the same sample, for clinical diagnosis and epidemiological survey. Three pairs of primers were designed and synthesized according to the published literatures in GenBank. And a triple PCR was developed to amplify conservative regions of each bacterial genomes of M. Bovis, M. mycoides subsp. mycoides Small Colony Type and M. agalactiae, with the target sequences of 448, 549 and 375 bp, respectively.Sensitivity of this triple PCR was analyzed. Specificity was verified with template from M. gallisepticum, M. Swine, M. agalactiae and M. mycoides subsp. mycoides Small Colony. And reliability was tested by comparing the results from determinative bacteriology. Three specific fragments of 448, 549 and 375 bp, corresponding to M. Bovis, M. mycoides subsp. mycoides Small Colony Type and M. agalactiae, were amplified under optimized condition, without interference between templates and the primers. And results were in agreement with determinative bacteriology. No band was shown in targeting genomes from M.
gallis epticum and M. Swine. Sensitivity was determined as 0. 8 ng ·μL-1. These results suggest that the triplex PCR could differentiate M. Bovlis, M. mycoides subsp. mycoides Small Colony Type and M. agalactiae based on one single sample, with high sensitivity, specificity and reliability,and can be applied in clinical diagnosis and epidemiological survey.%本研究旨在建立一种可一次性区分牛支原体、丝状支原体丝状亚种小克隆和无乳支原体的三重PCR诊断方法,为临床诊断和流行病学调查提供可靠检测技术.根据GenBank发表的上述3种病原的基因组序列保守区域设计3对特异性引物建立三重PCR方法;确定其检测敏感性,以猪支原体、鸡支原体、无乳支原体和丝状支原体丝状亚种小克隆基因作模板检验其特异性;同时和病原分离鉴定结果对比其准确性.结果表明在优化体系和条件下能够同时得到扩增长度为448、549、375 bp 3条特异性片段,未扩增出猪、鸡支原体模板特异性片段;其敏感性(可检测到的最小模板DNA含量)为0.8 ng·μL-1;36份临床样品检测结果显示,三重PCR检测结果与分离培养鉴定方法一致,均能鉴定出牛支原体阳性病料.本研究建立的三重PCR诊断方法能够一次性鉴别3种支原体,具有高敏感性、特异性和准确性,可用于临床诊断和流行病学调查.【总页数】5页(P306-310)
【作者】李大伟;黄灿平;张彦明;谢建华;冉智光;熊仲良;范伟兴
【作者单位】中国动物卫生与流行病学中心,青岛,266032;中国动物卫生与流行病学中心,青岛,266032;中国动物卫生与流行病学中心,青岛,266032;重庆市动物疫病预防控制中心,重庆,401147;重庆市动物疫病预防控制中心,重庆,401147;重庆市动物疫病预防控制中心,重庆,401147;中国动物卫生与流行病学中心,青岛,266032【正文语种】中文
【中图分类】S852.62
【相关文献】
1.绵羊肺炎支原体和丝状支原体双重PCR检测方法的建立 [J], 宋勤叶;李潭清;刘兰亚;刘月琴;张英杰
2.羊口疮病毒和丝状支原体簇双重PCR检测方法的建立及应用 [J], 林裕胜;江锦秀;江斌;游伟;胡奇林
3.丝状支原体丝状亚种SC生物型PCR检测方法的建议 [J], 辛九庆;高玉龙;杨婉容;王砚范
4.绵羊肺炎支原体、丝状支原体山羊亚种和山羊支原体山羊肺炎亚种多重PCR检测方法的建立 [J], 林裕胜;江锦秀;江斌;游伟;胡奇林
5.丝状支原体山羊亚种抗体间接血凝检测方法的建立及应用 [J], 储岳峰;逯忠新;赵萍;高鹏程;贺英;石琴
因版权原因,仅展示原文概要,查看原文内容请购买。

相关文档
最新文档