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作 者:杜雅楠 李静 刘艳成 杜鹏 包福祥 DU Ya-nan;LI Jing;LIU Yan-cheng;DU Peng;BAO Fu-xiang(Key Laboratory of Clinical Diagnosis and Treatment Technology in Animal Disease ,Ministry of Agriculture,College of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot, Inner Mongolia,010018,China;Xingan League Animal Disease Control Center,Ulanhot, Inner Mongolia ,137400,China)
机构地区:[1]内蒙古农业大学兽医学院/农业部动物疾病临床诊疗技术重点实验室,内蒙古呼和浩特010018 [2]兴安盟动物疫病预防控制中心,内蒙古乌兰浩特137400
出 处:《动物医学进展》2019年第9期29-33,共5页Progress In Veterinary Medicine
基 金:内蒙古自治区自然科学基金项目(980202);国家自然科学基金项目(81660297)
摘 要:为建立一种操作简便、准确率高的检测方法,对内蒙古地区猪传染性胃肠炎流行情况进行调查,参考GenBank中收录的猪传染性胃肠炎病毒的N基因序列,设计合成了一对特异性引物,针对该基因建立了TGEV的RT-PCR检测方法。应用建立的RT-PCR方法对从内蒙古地区7个盟市采集的204份猪腹泻样品进行了TGEV检测。结果显示,受检的204份样品中有24份样品呈现TGEV阳性,阳性率为11.76%。其中从赤峰市采集的样品TGEV阳性率最高,为20.83%;不同类型样品TGEV的检出率也有差异,其中肛门拭子的检出率最高(15.56%),其次是肠道样品(12.00%),粪便样品的检出率最低(7.87%)。表明所建立的RT-PCR检测方法灵敏度高、特异性强,可用于猪传染性胃肠炎病毒的快速检测。The research aimed to establish a simple and accurate method for detecting the epidemic situation of transmissible gastroenteritis virus in Inner Mongolia.A pair of specific primers were designed and synthesized according to the sequence of N gene of TGEV published in GenBank.The RT-PCR method was established according to N gene of TGEV.204 diarrhea fecal samples were collected from seven cities of Inner Mongolia,and tested by RT-PCR method.The results showed that 24 samples were TGEV positive,and the positive rate was 11.76%.The positive rate of samples collected from Chifeng city was the highest,up to 20.83%.The pathogen detection rate was different in the types of samples,therein TGEV detection rate of anal swab was the highest with 15.56%,the second was intestine,and the lowest was feces,and their positive rates of TGEV were 12.00% and 7.87%.The result showed that the method was highly sensitive and specific,and can be used for rapid detection of transmissible gastroenteritis virus.
关 键 词:猪传染性胃肠炎病毒 反转录-聚合酶链反应 检测
分 类 号:S852.659.6[农业科学—基础兽医学]
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