Premium
Phyllanthus amarus suppresses hepatitis B virus by interrupting interactions between HBV enhancer I and cellular transcription factors
Author(s) -
OTT M.,
THYAGARAJAN S. P.,
GUPTA S.
Publication year - 1997
Publication title -
european journal of clinical investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.164
H-Index - 107
eISSN - 1365-2362
pISSN - 0014-2972
DOI - 10.1046/j.1365-2362.1997.2020749.x
Subject(s) - enhancer , transcription (linguistics) , hepatitis b virus , biology , microbiology and biotechnology , transcription factor , transfection , woodchuck hepatitis virus , hbeag , enhancer rnas , in vitro , virology , hepadnaviridae , virus , gene , biochemistry , hbsag , linguistics , philosophy
The Phyllanthus amarus plant suppresses HBV mRNA transcription in vitro and exhibits therapeutic potential in chronic HBV carriers, although further work is necessary to define its mechanism of action. Analysis in HuH‐7 cells with transfected plasmids using a luciferase reporter showed that P. amarus specifically inhibited HBV enhancer I activity. To identify the mechanism of this HBV enhancer I inhibition, liver‐enriched cellular transcription factors were co‐expressed in HuH‐7 cells. The C/EBPα and β, as well as HNF‐3α and β transcription factors, significantly up‐regulated the HBV enhancer I activity. In contrast, co‐transfection of HNF‐1α or β had no effect upon the HBV enhancer I activity. Exposure to P. amarus inhibited C/EBPα‐ and β‐mediated up‐regulation of HBV enhancer I activity in a dose‐dependent manner, whereas HNF‐3α‐ and β‐mediated up‐regulation of HBV enhancer I was unaffected. In vitro gel shifts showed that P. amarus inhibited complexing of C/EBP transcription factors to a consensus oligonucleotide sequence, whereas DNA binding of AP‐1 and SP‐1 transcription factors was unaffected. As P. amarus down‐regulates HBV mRNA transcription by a specific mechanism involving interactions between HBV enhancer I and C/EBP transcription factors, purification and further analysis of the active P. amarus component will advance insights into its antiviral activity.