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原型沙粒病毒淋巴细胞性脉络丛脑膜炎病毒(LCMV)的致死性诱变

Lethal mutagenesis of the prototypic arenavirus lymphocytic choriomeningitis virus (LCMV).

作者信息

Ruiz-Jarabo Carmen M, Ly Calvin, Domingo Esteban, de la Torre Juan Carlos

机构信息

Centro de Biologia Molecular Severo Ochoa (CSIC, UAM), Universidad Autonoma de Madrid, Cantoblanco, 28049 Madrid, Spain.

出版信息

Virology. 2003 Mar 30;308(1):37-47. doi: 10.1016/s0042-6822(02)00046-6.

Abstract

Passage of the prototypic arenavirus lymphocytic choriomenigitis virus (LCMV) in cultured cells in the presence of the mutagenic agent 5-fluorouracil (FU) resulted in efficient and systematic virus extinction under conditions that did not significantly affect cell survival. FU-mediated extinction of LCMV was associated with 3.6- to 10-fold increases in the mutation frequencies for the three viral genes examined, but with only very modest effects on virus replication and transcription during a single round of infection. Likewise, FU did not affect expression of a LCMV minigenome. In contrast, the well documented antiviral effect of ribavirin against LCMV was not associated with significant increases in virus mutation frequencies, but rather with a dramatic inhibition of both viral RNA synthesis and LCMV minigenome expression. Mutagen induced viral extinction has been recently reported for positive strand RNA viruses polio and foot-and-mouth disease, and the lentivirus HIV-1. Our findings indicate that lethal mutagenesis can be effective also against LCMV, a negative strand RNA virus. Moreover, FU treatment prevented the establishment of LCMV persistent infection in mice deficient in B and T cells, suggesting the feasibility in vivo of lethal mutagenesis as a novel antiviral strategy.

摘要

在诱变剂5-氟尿嘧啶(FU)存在的情况下,原型沙粒病毒淋巴细胞性脉络丛脑膜炎病毒(LCMV)在培养细胞中传代,在对细胞存活没有显著影响的条件下导致病毒有效且系统性地灭绝。FU介导的LCMV灭绝与所检测的三个病毒基因的突变频率增加3.6至10倍相关,但在单轮感染期间对病毒复制和转录的影响非常小。同样,FU不影响LCMV微型基因组的表达。相比之下,利巴韦林对LCMV的抗病毒作用已得到充分证明,这与病毒突变频率的显著增加无关,而是与病毒RNA合成和LCMV微型基因组表达的显著抑制有关。最近报道了诱变剂诱导的正链RNA病毒脊髓灰质炎病毒和口蹄疫病毒以及慢病毒HIV-1的病毒灭绝。我们的研究结果表明,致死性诱变对负链RNA病毒LCMV也有效。此外,FU治疗可防止LCMV在B细胞和T细胞缺陷的小鼠中建立持续感染,这表明致死性诱变作为一种新型抗病毒策略在体内具有可行性。

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