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呼肠孤病毒Ⅲ型(Reo3)RT-PCR检测方法的建立

Development of A RT-PCR Method for Determination of Mammalian Orthoreovirus 3

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【作者】 王吉卫礼贺争鸣岳秉飞

【Author】 WANG Ji,WEI Li,HE Zheng-ming,YUE Bing-fei(National Institutes for food and drug Control,National Center for quality of Laboratory Animal,Beijing 100050,China)

【机构】 中国食品药品检定研究院、国家实验动物微生物遗传检测中心

【摘要】 目的建立呼肠孤病毒Ⅲ型(Reo3)RT-PCR检测方法,应用于实验动物及人用动物源性材料及生物制品外源Reo3的检测。方法根据已发表的呼肠孤病毒Ⅲ型(Reo3)M1基因序列,设计合成引物。提取Reo3细胞毒RNA,以其为模板,进行PCR扩增。优化反应条件,进行特异性、敏感性、重复性试验。结果建立的Reo3RT-PCR检测方法特异、敏感、稳定。以Reo3 RNA逆转录产物为模板,所能检测RNA最小模板浓度为0.42pg/μL,可检测病毒最小滴度为10-9/mL。结论建立的呼肠孤病毒Ⅲ型(Reo3)RT-PCR检测方法可用于实验动物及人用动物源性材料及生物制品外源Reo3的检测。

【Abstract】 Objective To develop a RT-PCR method for determination of Mammalian Orthoreovirus 3(Reo3) in laboratory animal and the biological materials or the biological products for human use from the animal.Methods Two pair of primers specific to the sequences of M1 gene were designed according to the published Mammalian Orthoreovirus 3.With which the RNA of Reo3 was extracted and reversely transcribed to cDNA as a template for PCR amplification.The developed RT-PCR method was optimized,verified for specificity and sensitivity.Results The developed RT-PCR method is good in ensitivity,specificity and stability,and its minimum detection limit using the recombinant plasmid containing Reo3 gene as atemplate was 0.42pg/μL,and the lowest detection virus titer is 10-9/mL.Conclusion The developed RT-PCR method can be used in detecting the Mammalian Orthoreovirus 3(Reo3) in laboratory animaland the biological materials or the biological products for human use from the animal.

【基金】 “国家科技支撑计划”疫苗类生物制品安全性评价技术研究(2008BAI54B01)
  • 【文献出处】 中国比较医学杂志 ,Chinese Journal of Comparative Medicine , 编辑部邮箱 ,2012年09期
  • 【分类号】R392.1
  • 【被引频次】7
  • 【下载频次】113
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