Suppression of mRNA accumulation by the duck hepatitis B virus reverse transcriptase

被引:11
作者
Cao, F
Tavis, JE
机构
[1] St Louis Univ, Sch Med, Dept Mol Microbiol & Immunol, St Louis, MO 63104 USA
[2] St Louis Univ, Sch Med, Ctr Liver, St Louis, MO 63104 USA
关键词
duck hepatitis B virus; gene regulation; viral replication; reverse transcriptase; polymerase; chronic infection; mRNA;
D O I
10.1016/j.virol.2006.02.026
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hepadnaviruses establish chronic liver infections, but the mechanisms of persistence and immune evasion are poorly understood. We previously found that the duck hepatitis B virus (DHBV) and hepatitis B virus reverse transcriptases (P protein) unexpectedly accumulate in the cytoplasm where they could affect function(s) beyond viral DNA synthesis, such as gene expression. Therefore, we measured effects of DHBV P on gene expression from reporter constructs and the viral genome. P reduced reporter expression at the mRNA level to similar to 30-40%, independent of reporter tested. Accumulation of the viral pregenomic RNA from its native promoter was suppressed three-to four-fold by P. and accumulation of the capsid protein and intracellular core particles was similarly suppressed because the pregenomic RNA encodes the capsid protein. Therefore, suppression of the pregenomic RNA by DHBV P creates a negative feedback loop to limit viral antigen accumulation and replication, possibly contributing to maintenance of chronic infection. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:475 / 483
页数:9
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