Inhibition of the Epstein-Barr virus lytic cycle by Zta-targeted RNA interference

被引:39
作者
Chang, Y
Chang, SS
Lee, HH
Doong, SL
Takada, K
Tsai, CH
机构
[1] Natl Taiwan Univ, Coll Med, Grad Inst Microbiol, Sect 1, Taipei 10764, Taiwan
[2] Hokkaido Univ, Inst Med Genet, Sapporo, Hokkaido, Japan
关键词
D O I
10.1099/vir.0.79886-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Epstein-Barr virus (EBV) reactivation into the lytic cycle plays certain roles in the development of EBV-associated diseases, so an effective strategy to block the viral lytic cycle may be of value to reduce the disease risk or to improve the clinical outcome. This study examined whether the EBV lytic cycle could be inhibited using RNA interference (RNAi) directed against the essential viral gene Zta. In cases of EBV reactivation triggered by chemicals or by exogenous Rta, Zta-targeted RNAi prevented the induction of Zta and its downstream genes and further blocked the lytic replication of viral genomes. This antiviral effect of RNAi was not likely to be mediated by activation of the interferon pathway, as phosphorylation of STAT1 was not induced. In addition, novel EBV-infected epithelial cells showing constitutive activation of the lytic cycle were cloned; such established lytic infection was also suppressed by Zta-targeted RNAi. These results indicate that RNAi can be used to inhibit the EBV lytic cycle effectively in vitro and could also be of potential use to develop anti-EBV treatments.
引用
收藏
页码:1371 / 1379
页数:9
相关论文
共 55 条
[1]   Epstein-Barr virus immediate-early proteins BZLF1 and BRLF1 activate the ATF2 transcription factor by increasing the levels of phosphorylated p38 and c-Jun N-terminal kinases [J].
Adamson, AL ;
Darr, D ;
Holley-Guthrie, E ;
Johnson, RA ;
Mauser, A ;
Swenson, J ;
Kenney, S .
JOURNAL OF VIROLOGY, 2000, 74 (03) :1224-1233
[2]   EXPRESSION OF PROTEINS ENCODED BY EPSTEIN-BARR-VIRUS TRANSACTIVATOR GENES DEPENDS ON THE DIFFERENTIATION OF EPITHELIAL-CELLS IN ORAL HAIRY LEUKOPLAKIA [J].
BECKER, J ;
LESER, U ;
MARSCHALL, M ;
LANGFORD, A ;
JILG, W ;
GELDERBLOM, H ;
REICHART, P ;
WOLF, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (19) :8332-8336
[3]   CHARACTERIZATION OF MACROMOLECULAR LIGNINS AS EPSTEIN-BARR-VIRUS INDUCER IN FOODSTUFF ASSOCIATED WITH NASOPHARYNGEAL CARCINOMA RISK [J].
BOUVIER, G ;
HERGENHAHN, M ;
POLACK, A ;
BORNKAMM, GW ;
DETHE, G ;
BARTSCH, H .
CARCINOGENESIS, 1995, 16 (08) :1879-1885
[4]   A system for stable expression of short interfering RNAs in mammalian cells [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
SCIENCE, 2002, 296 (5567) :550-553
[5]   Requirement for cell-to-cell contact in Epstein-Barr virus infection of nasopharyngeal carcinoma cells and keratinocytes [J].
Chang, Y ;
Tung, CH ;
Huang, YT ;
Lu, J ;
Chen, JY ;
Tsai, CH .
JOURNAL OF VIROLOGY, 1999, 73 (10) :8857-8866
[6]   Chromosomal integration of Epstein-Barr virus genomes in nasopharyngeal carcinoma cells [J].
Chang, Y ;
Cheng, SD ;
Tsai, CH .
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK, 2002, 24 (02) :143-150
[7]  
Chang Y, 1998, LAB INVEST, V78, P715
[8]   Serologic markers of Epstein-Barr virus infection and nasopharyngeal carcinoma in Taiwanese men [J].
Chien, YC ;
Chen, JY ;
Liu, MY ;
Yang, HI ;
Hsu, MM ;
Chen, CJ ;
Yang, CS .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (26) :1877-1882
[9]   AN ENHANCER WITHIN THE DIVERGENT PROMOTER OF EPSTEIN-BARR VIRUS RESPONDS SYNERGISTICALLY TO THE R-TRANSACTIVATORS AND Z-TRANSACTIVATORS [J].
COX, MA ;
LEAHY, J ;
HARDWICK, JM .
JOURNAL OF VIROLOGY, 1990, 64 (01) :313-321
[10]   PROGNOSTIC VALUE OF EBV MARKERS IN THE CLINICAL MANAGEMENT OF NASOPHARYNGEAL CARCINOMA (NPC) - A MULTICENTER FOLLOW-UP-STUDY [J].
DEVATHAIRE, F ;
SANCHOGARNIER, H ;
DETHE, H ;
PIEDDELOUP, C ;
SCHWAAB, G ;
HO, JHC ;
ELLOUZ, R ;
MICHEAU, C ;
CAMMOUN, M ;
CACHIN, Y ;
DETHE, G .
INTERNATIONAL JOURNAL OF CANCER, 1988, 42 (02) :176-181