Action of mutagenic agents and antiviral inhibitors on foot-and-mouth disease virus

被引:39
作者
Pariente, N
Sierra, S
Airaksinen, A
机构
[1] Univ Autonoma Madrid, CSIC, Ctr Biol Mol Severo Ochoa, E-28049 Madrid, Spain
[2] Univ Calif Los Angeles, AIDS Inst, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA
关键词
error catastrophe; lethal mutagenesis; foot-and-mouth disease virus; FMDV; fluorouracil; ribavirin; 5-azacytidine; mycophenolic acid; viral extinction; mutagen; inhibitor; picornavirus;
D O I
10.1016/j.virusres.2004.11.008
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Our current knowledge on foot-and-mouth disease virus (FMDV) entry into error catastrophe is reviewed. FMDV can establish cytolytic and persistent infections in the field and in cell culture. Both types of FMDV infection in cell culture can be treated with mutagens, with or without classical (non-mutagenic) antiviral inhibitors, to drive the virus to extinction. 5-Fluorouracil (FU) and 5-azacytidine (AZC) have been employed as mutagenic agents to treat cytolytic FMDV infections, and ribavirin (Rib) to treat persistent infections. Extinction is dependent on the relative fitness of the viral isolate, as well as on the viral load. In cytolytic infections, extinctions could be efficiently obtained with combinations of mutagens and inhibitors. High-fitness FMDV extinction could only be achieved with treatments that contained a mutagen, and not with combinations of inhibitors that exerted the same antiviral effect. Persistent infections could be cured with Rib treatment alone. The results presented here show entry into error catastrophe as a valid strategy for treatment of viral infections, although much work remains to be done before it can be implemented. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:183 / 193
页数:11
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