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口蹄疫病毒低保真度聚合酶突变体减毒。

Foot-and-mouth disease virus low-fidelity polymerase mutants are attenuated.

作者信息

Xie Xiaochun, Wang Haiwei, Zeng Jianxiong, Li Chen, Zhou Guohui, Yang Decheng, Yu Li

机构信息

Division of Livestock Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, No. 427 Maduan Street, Harbin, 150001, P. R. China.

出版信息

Arch Virol. 2014 Oct;159(10):2641-50. doi: 10.1007/s00705-014-2126-z. Epub 2014 Jun 3.

Abstract

Previous studies have shown that RNA viruses can be attenuated by either increased or decreased viral polymerase replication fidelity. Although foot-and-mouth disease virus (FMDV) high-fidelity RNA-dependent RNA polymerase (RdRp) variants with an attenuated phenotype have been isolated using mutagens, no FMDV mutant with a low-fidelity polymerase has been documented to date. Here, we describe the generation of several FMDV RdRp mutants using site-directed mutagenesis via a reverse genetic system. Mutation frequency assays confirmed that five rescued FMDV RdRp mutant populations had lower replication fidelity than the wild-type virus population, which allowed us to assess the effects of the change in replication fidelity on the virus phenotype. These low-fidelity FMDV RdRp mutants showed increased sensitivity to ribavirin or 5-fluorouracil (5-FU) treatment without a loss of growth capacity in cell cultures. In addition, decreased fitness and attenuated virulence were observed for the RdRp mutants with lower fidelity. Importantly, based on a quantitative analysis for fidelity and virulence, we concluded that lower replication fidelity is associated with a more attenuated virus phenotype. These results further contribute to our understanding of the replication fidelity of polymerases of RNA viruses and its relationship to virulence attenuation.

摘要

先前的研究表明,RNA病毒可通过提高或降低病毒聚合酶复制保真度来实现减毒。尽管使用诱变剂已分离出具有减毒表型的口蹄疫病毒(FMDV)高保真RNA依赖性RNA聚合酶(RdRp)变体,但迄今为止,尚未有低保真聚合酶的FMDV突变体的相关报道。在此,我们描述了通过反向遗传系统利用定点诱变产生几种FMDV RdRp突变体的过程。突变频率测定证实,五个拯救的FMDV RdRp突变体群体的复制保真度低于野生型病毒群体,这使我们能够评估复制保真度变化对病毒表型的影响。这些低保真FMDV RdRp突变体对利巴韦林或5-氟尿嘧啶(5-FU)处理表现出更高的敏感性,且在细胞培养中不失生长能力。此外,观察到保真度较低的RdRp突变体适应性降低且毒力减弱。重要的是,基于对保真度和毒力的定量分析,我们得出结论,较低的复制保真度与更减毒的病毒表型相关。这些结果进一步有助于我们理解RNA病毒聚合酶的复制保真度及其与毒力减弱的关系。

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