The use of RNAi and transgenics to develop viral disease resistant livestock.

T G Wise, D S Schafer, J W Lowenthal, T J Doran
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引用次数: 21

Abstract

The possibility of genetically engineering poultry to make them resistant to avian influenza is attracting attention and has now become a real possibility with improved methods for genetic modification and the emergence of RNAi as an antiviral strategy. In order to test this possibility, we have generated transgenic mice that express RNAi molecules targeting a conserved region of the influenza A NP gene and are testing these mice for resistance to influenza infection. Transgenes were initially developed that express short hairpin RNAs (shRNAs) targeting multiple influenza A viral genes. The shRNAs were tested for inhibition of H1N1 PR8 virus in vitro. Two potent shRNAs that target the NP and PA genes were chosen for lentiviral mediated generation of transgenic mice. Transgenic founders for the NP shRNA construct and also a negative control shRNAtargeting EGFP were generated. The constitutive expression of the shRNA molecules in a range of tissue types including lung, was confirmed and so far stable transmission of the RNAi transgenes from the F0 to F3 generation has been observed. Resistance to influenza infection in these transgenic mice is now being confirmed.

利用RNAi和转基因技术培育抗病毒家畜。
对家禽进行基因工程以使其对禽流感具有抵抗力的可能性正在引起人们的注意,随着基因修饰方法的改进和RNAi作为抗病毒策略的出现,这种可能性现在已经成为一种真正的可能性。为了测试这种可能性,我们已经产生了表达RNAi分子靶向流感a NP基因保守区域的转基因小鼠,并正在测试这些小鼠对流感感染的抵抗力。转基因最初是通过表达针对多种甲型流感病毒基因的短发夹rna (shRNAs)而开发的。在体外测试了这些shrna对H1N1 PR8病毒的抑制作用。选择了两个靶向NP和PA基因的强效shrna用于慢病毒介导的转基因小鼠的产生。产生了NP shRNA构建物的转基因奠基物和一个阴性对照的靶向EGFP的shRNA。shRNA分子在包括肺在内的一系列组织类型中的组成性表达已被证实,到目前为止,RNAi转基因从F0代到F3代的稳定传播已被观察到。这些转基因小鼠对流感感染的抵抗力现已得到证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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