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我国犬钩虫ITS及5.8S rDNA的克隆与序列分析
引用本文:宋慧群,李宾,林瑞庆,朱兴全. 我国犬钩虫ITS及5.8S rDNA的克隆与序列分析[J]. 中国兽医科学, 2007, 37(9): 756-759
作者姓名:宋慧群  李宾  林瑞庆  朱兴全
作者单位:华南农业大学,兽医学院,广东,广州,510642
摘    要:以从我国广东湛江犬小肠中采集的2条犬钩虫作为研究对象,用保守引物NC5及NC2扩增犬钩虫rDNA的ITS-1、5.8S及ITS-2片段,将PCR扩增出的片段纯化后克隆至pGEM-T Easy载体,重组质粒通过菌落PCR和酶切鉴定后,对阳性菌落进行序列测定并进行序列分析。结果显示,来自湛江的2条犬钩虫ITS及5.8S rDNA序列总长均为738 bp,其中ITS-1序列长为364 bp,5.8S序列长为153 bp,ITS-2序列长为221 bp;2个不同样品之间ITS序列存在多态性,ITS-1序列存在5个碱基的差异,ITS-2序列存在1个碱基的差异,5.8S rDNA序列无差异。研究结果为犬钩虫进一步的分类、鉴定和遗传变异研究奠定了基础。

关 键 词:犬钩虫  内转录间隔区(ITS)  序列分析
文章编号:1673-4696(2007)09-0756-04
修稿时间:2007-07-09

Cloning and sequence analysis of the ITS and 5.8S rDNA of Ancylostoma caninum in China
SONG Hui-qun,LI Bin,LIN Rui-qing,ZHU Xing-quan. Cloning and sequence analysis of the ITS and 5.8S rDNA of Ancylostoma caninum in China[J]. Chinese Veterinary Science, 2007, 37(9): 756-759
Authors:SONG Hui-qun  LI Bin  LIN Rui-qing  ZHU Xing-quan
Abstract:The internal transcribed spacer(ITS) and 5.8S rDNA of Ancylostoma caninum isolated in Guangdong Province of China were amplified by PCR using a pair of conserved primers and the amplicons were cloned into pGEM-T Easy vector,respectively.The inserts were successfully sequenced,and the ITS of the two A.caninum samples was 738 bp in length.Sequence analysis revealed that the ITS-1,5.8S and ITS-2 rDNA of both A.caninum samples were 364 bp,153 bp and 221 bp in length,respectively,and polymorphism was found in the ITS-1 and ITS-2 rDNA sequences between the two A.caninum samples.The results provided a foundation for further studies of molecular identification and molecular genetics of A.caninum.
Keywords:5.8S rDNA  PCR
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