›› 2013, Vol. 40 ›› Issue (12): 12-20.

• 生物技术 • 上一篇    下一篇

shRNA抑制猪繁殖与呼吸综合征病毒(PRRSV)JXA1-R株在Marc-145细胞中复制及抗PRRSV细胞株的建立

李红梅1,2, 贺聪2, 张茂3, 孟轩2, 张建峰2, 张健騑2, 郭鹏举2   

  1. 1. 华南农业大学动物科学学院, 广东广州 510642;
    2. 广东省农业科学院动物卫生研究所公共实验室, 广东广州 510640;
    3. 广东省农业科学院动物科学研究所, 广东广州 510640
  • 收稿日期:2013-05-17 出版日期:2013-12-20 发布日期:2014-02-11
  • 作者简介:李红梅(1980- ),女,山西人,博士,讲师,研究方向:畜禽传染病及抗病育种。
  • 基金资助:
    农业部948项目(2011-Z56)。

Inhibition of Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) JXA1-R Replication in Marc-145 Cells by shRNA and Establishment of Anti-PRRSV Cell Lines

LI Hong-mei1,2, HE Cong2, ZHANG Mao3, MENG Xuan2, ZHANG Jian-feng2, ZHANG Jian-fei2, GUO Peng-ju2   

  1. 1. College of Animal Science, South China Agricultural University, Guangzhou 510642, China;
    2. Public Laboratory, Institute of Animal Health, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China;
    3. Institute of Animal Science, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China
  • Received:2013-05-17 Online:2013-12-20 Published:2014-02-11

摘要: 猪繁殖与呼吸综合征(porcine reproductive and respiratory syndrome,PRRS)是世界上主要的猪传染性疾病之一,目前,疫苗和抗病毒药物只能提供有限的保护。本研究选择猪繁殖与呼吸综合征病毒(porcine reproductive and respiratory syndrome virus,PRRSV)JXA1-R株ORF1a、ORF3、ORF4、ORF5、ORF6、ORF7的保守区域为靶序列,利用pSilencer2.1-U6 neo构建shRNA表达载体并转染Marc-145细胞。经实时荧光定量PCR、细胞病变及病毒滴度分析,结果显示,ORF1a-4-shRNA、ORF3-1-shRNA、ORF6-2-shRNA干扰质粒能明显抑制病毒基因的转录,并有效抑制PRRSV在Marc-145上的增殖,显著降低病毒滴度。最后筛选ORF6-2-shRNA表达质粒转染猪胎儿成纤维细胞,构建稳定转染细胞株,为抗PRRSV转基因猪的生产奠定了基础。

关键词: 猪繁殖与呼吸综合征病毒; RNA干扰; 抗猪繁殖与呼吸综合征病毒细胞株

Abstract: Porcine reproductive and respiratory syndrome (PRRS) was one of the most important infectious diseases of swine in the world.However,current vaccination strategies and antiviral drugs provided only limited protection. In this study, the ability of specific short hairpin RNA targeting to ORF1a, ORF3, ORF4, ORF5, ORF6, ORF7 were constructed, and it was found that ORF1a-4-shRNA, ORF3-1-shRNA, ORF6-2-shRNA could effectively down-regulate specific gene expression and inhibit viral replication in Marc-145 cells compared to the controls. In addition, in this study ORF6-2-shRNA was selected to be transfected into porcine fetal fibroblasts to establish anti-PRRSV cell lines. This work might provide the foundation for further research on the production of anti-PRRSV transgenetic pig.

Key words: porcine reproductive and respiratory syndrome virus (PRRSV); RNA interference; anti-PRRSV cell lines

中图分类号: