Small Interfering RNA Inhibition of Andes Virus Replication

被引:8
作者
Chiang, Cheng-Feng [1 ]
Albarino, Cesar G. [1 ]
Lo, Michael K. [1 ]
Spiropoulou, Christina F. [1 ]
机构
[1] Ctr Dis Control & Prevent, Viral Special Pathogens Branch, Div High Consequence Pathogens & Pathol, Atlanta, GA 30333 USA
关键词
HANTAVIRUS CARDIOPULMONARY SYNDROME; PULMONARY SYNDROME; NUCLEOCAPSID PROTEIN; ANTIVIRAL IMMUNITY; MOSQUITO CELLS; DOUBLE-BLIND; TRANSMISSION; INFECTIONS; RESISTANCE; RIBAVIRIN;
D O I
10.1371/journal.pone.0099764
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Andes virus (ANDV) is the most common causative agent of hantavirus pulmonary syndrome (HPS) in the Americas, and is the only hantavirus associated with human-to-human transmission. Case fatality rates of ANDV-induced HPS are approximately 40%. There are currently no effective vaccines or antivirals against ANDV. Since HPS severity correlates with viral load, we tested small interfering RNA (siRNA) directed against ANDV genes as a potential antiviral strategy. We designed pools of 4 siRNAs targeting each of the ANDV genome segments (S, M, and L), and tested their efficacy in reducing viral replication in vitro. The siRNA pool targeting the S segment reduced viral transcription and replication in Vero-E6 cells more efficiently than those targeting the M and L segments. In contrast, siRNAs targeting the S, M, or L segment were similar in their ability to reduce viral replication in human lung microvascular endothelial cells. Importantly, these siRNAs inhibit ANDV replication even if given after infection. Taken together, our findings indicate that siRNAs targeting the ANDV genome efficiently inhibit ANDV replication, and show promise as a strategy for developing therapeutics against ANDV infection.
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