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敏感性PCR检测猪肉弓形虫方法的建立与应用
引用本文:余莉,朱新伊,胡元生,张俊玲,罗庆礼,沈继龙.敏感性PCR检测猪肉弓形虫方法的建立与应用[J].中国人兽共患病杂志,2010,26(10):895-899.
作者姓名:余莉  朱新伊  胡元生  张俊玲  罗庆礼  沈继龙
作者单位:安徽医科大学病原生物学教研室人兽共患病安徽省重点实验室;安徽医科大学第三附属医院检验科;
基金项目:国家自然科学基金青年基金,安徽省教育厅高校自然科学基金 
摘    要:目的建立一种敏感快速的猪肉弓形虫PCR检测方法,并用来检测市售猪肉弓形虫的感染情况。方法采用不同数量的弓形虫模拟感染猪肉样本,分别以529 bp重复序列、B1基因、SAG1、SAG2、SAG3作为目标检测基因,对其敏感性进行评价,在此基础上运用敏感的靶标检测100份市售猪肉样本中弓形虫的感染情况。结果 529 bp重复序列的敏感性最高,用此靶标检测合肥市售猪肉,弓形虫阳性率为17%。结论 529 bp重复序列基因是一个可用于肉制品中弓形虫PCR检测的理想靶标。

关 键 词:弓形虫  PCR  猪肉  
收稿时间:2010-10-20

Establishment and application on a sensitive PCR assay for detection of Toxoplasma gondii in retail pork
YU Li,ZHU Xin-yi,HU Yuan-sheng,ZHANG Jun-ling,LUO Qing-li,SHEN Ji-long.Establishment and application on a sensitive PCR assay for detection of Toxoplasma gondii in retail pork[J].Chinese Journal of Zoonoses,2010,26(10):895-899.
Authors:YU Li  ZHU Xin-yi  HU Yuan-sheng  ZHANG Jun-ling  LUO Qing-li  SHEN Ji-long
Affiliation:(Department of Microbiology and Parasitology,Anhui Medical University,Hefei 230032,China)
Abstract:A sensitive PCR assay for detection of Toxoplasma gondii(T.gondii) was developed and evaluated in retail pork infeeted with T.gondii.Pork samples were contaminated artificially by different amounts of T.gondii tachyzoite(0-10 000),and the 529 bp repetitive sequence(Toxo-529),B1 gene,SAG1,SAG2,and SAG3 of T.gondii were used as detecting targets respectively.Sensitivity of target genes was evaluated,and results indicated that the 529 bp repetitive sequence was the most sensitive target among these candidate genes.Then,100 retail pork samples were collected to analyze T.gondii contamination and the positive rate for T.gondii DNA fragments was about 17%.These results demonstrate that the 529 bp repetitive sequence is a sensitive target gene for PCR detection of T.gondii in retail pork.
Keywords:PCR
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