Inhibition of Junin virus replication by small interfering RNAs

被引:17
|
作者
Artuso, Maria C. [1 ]
Ellenberg, Paula C. [1 ]
Scolaro, Luis A. [1 ]
Damonte, Elsa B. [1 ]
Garcia, Cybele C. [1 ]
机构
[1] Univ Buenos Aires, Virol Lab, Dept Biol Chem, Sch Sci, RA-1428 Buenos Aires, DF, Argentina
关键词
Junin virus; Arenavirus; Matrix protein; RNA interference; siRNAs; LYMPHOCYTIC CHORIOMENINGITIS VIRUS; FINGER-Z-PROTEIN; ZINC-BINDING PROTEIN; MESSENGER-RNA; ANTIVIRAL THERAPY; LASSA-VIRUS; CELLS; ARENAVIRUSES; EXPRESSION; SIRNA;
D O I
10.1016/j.antiviral.2009.07.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Junin virus (JUNV), the etiological agent of the Argentine hemorrhagic fever, has a single-stranded RNA genome with ambisense expression which encodes for five proteins. In previous works we have demonstrated that the Z arenavirus matrix protein represents an attractive target for antiviral therapy. With the aim of studying a new alternative therapeutic mechanism, four Z-specific siRNAs (Z1 - to Z4-siRNAs) were tested showing variable efficacy. The most effective inhibitor was Z2-siRNA targeted at the region encompassed by nt 179-197 of Z gene. The efficacy of this Z2-siRNA against JUNV was also demonstrated in virus-infected cells, by testing infectious virus plaque formation (92.8% JUNV yield reduction), viral RNA level or antigen expression, as well as in cells transfected with Z-specific reporter plasmids (91% reduction in expression of Z-EGFP fusion protein). Furthermore, the lack of effect of this Z-siRNA on the expression of other JUNV proteins, such as N and GPC, confirmed the specificity of action exerted by Z2-siRNA on Z transcript. Thus, the present study represents the first report of vir-us inhibition mediated by RNA interference for a New World arenavirus. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:31 / 37
页数:7
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