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PCR-RFLP和特异PCR技术用于鲁道夫对盲囊线虫鉴定的研究
引用本文:何芳,屈仁建,杨廷宝,宋慧群,吴绍强,林瑞庆,朱兴全.PCR-RFLP和特异PCR技术用于鲁道夫对盲囊线虫鉴定的研究[J].中国兽医杂志,2005,41(9):3-5.
作者姓名:何芳  屈仁建  杨廷宝  宋慧群  吴绍强  林瑞庆  朱兴全
作者单位:1. 华南农业大学兽医学院,广东,广州,510642
2. 山西恒丰强动物药业有限公司广州分公司,广东,广州,510650
3. 中山大学生命科学学院,广东,广州,510275
基金项目:国家杰出青年科学基金项目(30225033)
摘    要:本研究运用新建立的Contracaecum rudolphii姊妹种的PCR-RFLP和特异PCR鉴定方法对来自我国青海湖的鲁道夫对盲囊线虫进行分子鉴定。经PCR-RFLP分析,来自我国青海湖的鲁道夫对盲囊线虫的两个样品的带型与C.rudolphiiB的酶切带型一致。经特异PCR扩增,C.rudolphii B的特异引物能从我国鲁道夫对盲囊线虫中扩增出目的片段,与对照C.rudolphii B的代表样品扩增片段大小相同。该两种方法试验结果都说明来自我国青海湖的对盲囊线虫为C.rudolphii B,与PCR-SSCP方法鉴定结果一致。本次研究结果及所建立的分子分类学方法为我国异尖线虫的进一步研究奠定了基础。

关 键 词:鲁道夫对盲囊线虫  PCR-RFLP  特异PCR  鉴定
文章编号:0529-6005(2005)09-0003-03
收稿时间:11 28 2004 12:00AM
修稿时间:2004年11月28

Determination of specific status of Contracaecum rudolphii from China by PCR-RFLP and Specific PCR assays
HE Fang,QU Ren-jian,YANG Ting-bao,SONG Hui-qun,WU Shao-qiang,LIN Rui-qing,ZHU Xing-quan.Determination of specific status of Contracaecum rudolphii from China by PCR-RFLP and Specific PCR assays[J].Chinese Journal of Veterinary Medicine,2005,41(9):3-5.
Authors:HE Fang  QU Ren-jian  YANG Ting-bao  SONG Hui-qun  WU Shao-qiang  LIN Rui-qing  ZHU Xing-quan
Abstract:The present study was designed to determine the specific status of specimens representing Contracaecum rudolphii, collected from Qinghai Lake in China, by PCR-linked restriction fragment length polymorphism (PCR-RFLP) and specific PCR assays. The result of PCR-RFLP analysis revealed that the restriction profiles of C. rudolphii specimens from China were identical to that of C. rudolphii B. Specific amplicons were amplified from the Chinese C. rudolphii specimens using the C. rudolphii B-specific primers, identical in lengh to that of C. rudolphii B. These findings indicated that C. rudolphii specimens from China represented C. rudolphii B. The findings of the presented study and the two molecular assays taken have implications for studying the systematics and molecular genetics of anisakid nematodes from China.
Keywords:Contracaecum rudolphii  PCR-RFLP  specific PCR  identification
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