Antiviral potency of a siRNA targeting a conserved region of coxsackievirus A24

被引:12
作者
Jun, Eun Jung [1 ,3 ]
Nam, Young Ran [1 ,3 ]
Ahn, Jeonghyun [1 ,3 ]
Tchah, Hungwon [2 ,3 ]
Joo, Chul Hyun [1 ,3 ]
Jee, Youngmee [4 ]
Kim, Yoo Kyum [1 ,3 ]
Lee, Heuiran [1 ,3 ]
机构
[1] Univ Ulsan, Coll Med, Dept Microbiol, Seoul, South Korea
[2] Univ Ulsan, Coll Med, Dept Ophthalmol, Seoul, South Korea
[3] Univ Ulsan, Coll Med, Res Inst Biomacromol, Seoul, South Korea
[4] Minist Hlth & Welf, Korea Ctr Dis Control & Prevent, Natl Inst Hlth, Dept Virol,Div Enter & Hepatitis Viruses, Seoul, South Korea
关键词
Coxsackievirus A24; Acute hemorrhagic conjunctivitis; Small-interfering RNA; Antiviral effect; cis-Acting replication element;
D O I
10.1016/j.bbrc.2008.08.169
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Coxsackievirus A24 (CVA24) is responsible for acute hemorrhagic conjunctivitis, a highly contagious eye disease for which no prevention or treatment is Currently available. We thus assessed the antiviral potential of a small interfering RNA (siRNA) targeting CVA24. HeLa cells with or without four different siRNAs complementary to 2C or 3D genome region, were challenged with various CVA24s. Among several siRNAs, a siRNA targeting the highly conserved genome region called the cis-acting replication element (CVA24-CRE), was the only siRNA that decreased virus replication and Subsequent cytotoxicity by both CVA24 variant and clinical isolates. Furthermore, CVA24-CRE had effective antiviral activity against CVA24 in primary human conjunctival cells. In addition, CVA24-CRE was highly resistant to the emergence of genetically altered escape mutants. Collectively, the present Study provides evidence that CVA24-CRE targeting a conserved viral genome region had universal, prolonged anti-CVA24 activity. This siRNA may thus hold a potential to act clinically as a novel anti-CVA24 agent. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:389 / 394
页数:6
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