您好，欢迎访问中国农业科学院 机构知识库！

全部

  • 全部
  • 标题
  • 学者
  • 机构
  • 关键词

Amber codon is genetically unstable in generation of premature termination codon (PTC)-harbouring Foot-and-mouth disease virus (FMDV) via genetic code expansion

文献类型： 外文期刊

作者： Hao, Rongzeng 1 ; Ma, Kun 1 ; Ru, Yi 1 ; Li, Dan 1 ; Song, Gaoyuan 1 ; Lu, Bingzhou 1 ; Liu, Huanan 1 ; Li, Yajun 1 ; Zhang, 1 ;

作者机构： 1.Chinese Acad Agr Sci, OIE Natl Foot & Mouth Dis Reference Lab, Lanzhou Vet Res Inst, State Key Lab Vet Etiol Biol, Lanzhou, Peoples R China

2.Univ Texas Med Branch UTMB, Sealy Ctr Vaccine Dev, Dept Microbiol & Immunol, Galveston, TX USA

3.Univ Texas Med Branch UTMB, Inst Human Infect & Immun, Galveston, TX USA

关键词： Amber codon; genetic code expansion; premature termination codon (ptc); foot-and-mouth disease virus; genetic stability

期刊名称：RNA BIOLOGY （ 影响因子：5.35； 五年影响因子：5.414 ）

ISSN： 1547-6286

年卷期：

页码：

收录情况： SCI

摘要： The foot-and-mouth disease virus (FMDV) is the causative agent of FMD, a highly infectious and devastating viral disease of domestic and wild cloven-hoofed animals. FMD affects livestock and animal products' national and international trade, causing severe economic losses and social consequences. Currently, inactivated vaccines play a vital role in FMD control, but they have several limitations. The genetic code expansion technology provides powerful strategies for generating premature termination codon (PTC)-harbouring virus as a live but replication-incompetent viral vaccine. However, this technology has not been explored for the design and development of new FMD vaccines. In this study, we first expanded the genetic code of the FMDV genome via a transgenic cell line containing an orthogonal translation machinery. We demonstrated that the transgenic cells stably integrated the orthogonal pyltRNA/pylRS pair into the genome and enabled efficient, homogeneous incorporation of unnatural amino acids into target proteins in mammalian cells. Next, we constructed 129 single-PTC FMDV mutants and four dual-PTC FMDV mutants after considering the tolerance, location, and potential functions of those mutated sites. Amber stop codons individually substituted the selected amino acid codons in four viral proteins (3D, L, VP1, and VP4) of FMDV. We successfully rescued PTC-FMDV mutants, but the amber codon unexpectedly showed a highly degree of mutation rate during PTC-FMDV packaging and replication. Our findings highlight that the genetic code expansion technology for the generation of PTC-FMD vaccines needs to be further improved and that the genetic stability of amber codons during the packaging and replication of FMDV is a concern.

  • 相关文献
作者其他论文 更多>>
置顶
购物车
反馈

© 京ICP备09089781号-29 主办单位：中国农业科学院

学术资源： 中国农业科学院 农业专业知识服务系统 农科联盟资源共建共享平台 中国农业科技文献与信息服务平台 中国农业期刊集成服务平台