鉴别猪瘟野毒与疫苗毒的单一与二重RT-PCR检测方法的建立及应用

doi:10.16431/j.cnki.1671-7236.2016.09.003

《中国畜牧兽医》 ›› 2016, Vol. 43 ›› Issue (9): 2230-2239.doi: 10.16431/j.cnki.1671-7236.2016.09.003

鉴别猪瘟野毒与疫苗毒的单一与二重RT-PCR检测方法的建立及应用

马萍^1,2, 李达¹, 汤德元¹, 张元鑫², 张华², 曾智勇¹, 刘霞², 韦冠东¹

1. 贵州大学动物科学学院, 贵阳 550025;
2. 贵州省动物疫病预防控制中心, 贵阳 550008

收稿日期:2016-01-16 出版日期:2016-09-20 发布日期:2016-09-20
通讯作者: 汤德元 E-mail:tdyuan@163.com
作者简介:马萍(1969-),女,贵州遵义人,硕士,高级兽医师,研究方向:动物疫病诊断防控,E-mail:zhouyikong2012@163.com
基金资助:
贵州省2014年农业攻关项目（黔科合NY字[2014]3055号）；贵州省科学技术基金项目（黔科合J字[2013]2110号）；贵州大学研究生创新基金（农研[2015]030号）

Establishment and Application of Single and Duplex RT-PCR Method for Differentiation of Wild-type and Vaccine Viruses of Classical Swine Fever Virus

MA Ping^1,2, LI Da¹, TANG De-yuan¹, ZHANG Yuan-xin², ZHANG Hua², ZENG Zhi-yong¹, LIU Xia², WEI Guan-dong¹

1. Department of Animal Science, Guizhou University, Guiyang 550025, China;
2. Animal Disease Prevention and Control Center in Guizhou Province, Guiyang 550008, China

Received:2016-01-16 Online:2016-09-20 Published:2016-09-20

摘要/Abstract

摘要：

为建立一种对猪瘟病毒（classical swine fever virus，CSFV）临床样本快速、简便的检测技术，以区分猪瘟（classical swine fever，CSF）野毒和疫苗毒感染，为规模化猪场CSF净化奠定基础。通过对GenBank中CSF野毒、疫苗毒及近源病毒的基因组全序列比对，发现CSF兔化弱毒疫苗株3’-NTR独立存在富含T的插入序列，根据这一特点分别在该插入序列的上、下两端设计2对单一RT-PCR引物并选择特异保守区域设计了二重RT-PCR引物，优化筛选能够鉴别CSF野毒与兔化弱毒疫苗的PCR反应条件，建立了能鉴别CSF野毒和疫苗毒的单一与二重RT-PCR鉴别诊断方法。敏感性和特异性分析表明，单一RT-PCR检测CSFV各引物最低核酸检测量分别为2.2 pg（单一RT-PCR中的1对引物）和1.7 pg（单一RT-PCR中的另外1对引物）；二重RT-PCR检测CSFV各引物最低核酸检测量分别为8.2 pg（CSF野毒）和6.7 pg（CSF疫苗毒），两种方法均检测不到PRV、PRRSV、JEV、BVDV、PCV2的DNA/RNA。采用该方法对146份可疑临床样品进行检测，结果表明CSF疫苗毒与野毒在能繁母猪、育肥猪、保育猪和哺乳仔猪中的二重感染率分别为6.3%、7.4%、8.3%、8.6%。本研究建立的单一与二重RT-PCR方法都具有敏感性强、特异性优、重复性好的特点，该研究对规模化猪场猪瘟的净化具有十分重要的参考价值。

关键词: 猪瘟病毒; 野毒; 疫苗毒; 单一RT-PCR; 二重RT-PCR; 鉴别诊断; 净化应用

Abstract:

For the distinguishment of wild-type and vaccine viruses of classical swine fever (CSF),a rapid and simple method was established,which laid the foundation for the purification of classical swine fever virus (CSFV) in large-scale farms.It was found that T-rich insertion sequence independently that 3'-NTR in Lapinized vaccine strain according to the genome sequence comparative analysis of CSF wild virus,vaccine virus and near origin virus published in GenBank,on the basis of this,two pairs of specific primers were designed in the upper and lower ends of the insertion sequence and duplex RT-PCR primers were designed.The anneal temperature of polymerese chain reaction (PCR) was optimized,then the two single and duplex RT-PCR method for the differentiation of wild-type and vaccine viruses of CSF were established.The sensitivity and specificity results showed that the minimum amounts of nucleic acid by the single RT-PCR were 2.2 pg (one pair of primers in single RT-PCR)and 1.7 pg (another pair of primers in single RT-PCR),respectively,and that of the duplex RT-PCR were 8.2 pg (wild-type virus of CSF) and 6.7 pg (vaccine virus of CSF), respectively, and no amplification of PRV,PRRSV,JEV,BVDV,PCV2 DNA/RNA were detected by these methods.Then the methods were used to detect 146 suspicious clinical samples,and the results showed that the positive rates of the mixed infection by wild-type and vaccine viruses of CSF in breeding sows,fattening pigs,nursery pigs and suckling piglets were 6.3%,7.4%,8.3%,8.6%, respectively.The results indicated that the single and duplex RT-PCR methods had high specificity,sensitivity,and good repeatability,and it had an important reference value for the purification of CSF in large-scale farms.

Key words: classsical swine fever virus; wild-type; vaccine viruses; single RT-PCR; duplex RT-PCR; differential diagnosis; purification and application

中图分类号:

S852.65⁺1

马萍, 李达, 汤德元, 张元鑫, 张华, 曾智勇, 刘霞, 韦冠东. 鉴别猪瘟野毒与疫苗毒的单一与二重RT-PCR检测方法的建立及应用[J]. 《中国畜牧兽医》, 2016, 43(9): 2230-2239.

MA Ping, LI Da, TANG De-yuan, ZHANG Yuan-xin, ZHANG Hua, ZENG Zhi-yong, LIU Xia, WEI Guan-dong. Establishment and Application of Single and Duplex RT-PCR Method for Differentiation of Wild-type and Vaccine Viruses of Classical Swine Fever Virus[J]. , 2016, 43(9): 2230-2239.

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鉴别猪瘟野毒与疫苗毒的单一与二重RT-PCR检测方法的建立及应用

Establishment and Application of Single and Duplex RT-PCR Method for Differentiation of Wild-type and Vaccine Viruses of Classical Swine Fever Virus

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