Antihepatitis B Virus Activity of a Protein-Enriched Fraction from Housefly (Musca domestica) in a Stable HBV-Producing Cell Line
Hepatitis B virus (HBV) infection remains a major public health problem. Although several vaccines and therapeutic strategies are currently being implemented to combat HBV virus, effective antiviral therapy against HBV infection has not been fully developed. Alternative strategies and new drugs to c...
Saved in:
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2014-01-01
|
Series: | The Scientific World Journal |
Online Access: | http://dx.doi.org/10.1155/2014/389560 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832548668666806272 |
---|---|
author | Xuemei Lu Xiaobao Jin Jie Wang Fujiang Chu Jiayong Zhu |
author_facet | Xuemei Lu Xiaobao Jin Jie Wang Fujiang Chu Jiayong Zhu |
author_sort | Xuemei Lu |
collection | DOAJ |
description | Hepatitis B virus (HBV) infection remains a major public health problem. Although several vaccines and therapeutic strategies are currently being implemented to combat HBV virus, effective antiviral therapy against HBV infection has not been fully developed. Alternative strategies and new drugs to combat this disease are urged. Insects and insect derivatives are a large and unexploited source of potentially useful compounds for modern medicine. In the present study, we investigated the first anti-HBV activity of a protein-enriched fraction (PE) from the larvae of the housefly (Musca domestica) in a stable HBV-producing cell line. HBsAg and HBeAg in the culture medium were measured by enzyme-linked immunosorbent assay. HBV-DNA was quantified by fluorescent quantification PCR. HBV core protein was assayed by immunofluorescent staining. Results indicate PE treatment inhibited both HBsAg, HBeAg secretion, and HBV-DNA replication. Furthermore, PE could also suppress HBV core protein expression. PE could be a potential candidate for the development of a novel and effective drug for the treatment of HBV infection. |
format | Article |
id | doaj-art-3343e64031ce47c2b432dab15b0ddc13 |
institution | Kabale University |
issn | 2356-6140 1537-744X |
language | English |
publishDate | 2014-01-01 |
publisher | Wiley |
record_format | Article |
series | The Scientific World Journal |
spelling | doaj-art-3343e64031ce47c2b432dab15b0ddc132025-02-03T06:13:19ZengWileyThe Scientific World Journal2356-61401537-744X2014-01-01201410.1155/2014/389560389560Antihepatitis B Virus Activity of a Protein-Enriched Fraction from Housefly (Musca domestica) in a Stable HBV-Producing Cell LineXuemei Lu0Xiaobao Jin1Jie Wang2Fujiang Chu3Jiayong Zhu4Guangdong Provincial Key Laboratory of Pharmaceutical Bioactive Substances, Guangzhou Higher Education Mega Center, Guangdong Pharmaceutical University, 280 Wai Huan Dong Road, Guangzhou 510006, ChinaGuangdong Provincial Key Laboratory of Pharmaceutical Bioactive Substances, Guangzhou Higher Education Mega Center, Guangdong Pharmaceutical University, 280 Wai Huan Dong Road, Guangzhou 510006, ChinaGuangdong Provincial Key Laboratory of Pharmaceutical Bioactive Substances, Guangzhou Higher Education Mega Center, Guangdong Pharmaceutical University, 280 Wai Huan Dong Road, Guangzhou 510006, ChinaGuangdong Provincial Key Laboratory of Pharmaceutical Bioactive Substances, Guangzhou Higher Education Mega Center, Guangdong Pharmaceutical University, 280 Wai Huan Dong Road, Guangzhou 510006, ChinaGuangdong Provincial Key Laboratory of Pharmaceutical Bioactive Substances, Guangzhou Higher Education Mega Center, Guangdong Pharmaceutical University, 280 Wai Huan Dong Road, Guangzhou 510006, ChinaHepatitis B virus (HBV) infection remains a major public health problem. Although several vaccines and therapeutic strategies are currently being implemented to combat HBV virus, effective antiviral therapy against HBV infection has not been fully developed. Alternative strategies and new drugs to combat this disease are urged. Insects and insect derivatives are a large and unexploited source of potentially useful compounds for modern medicine. In the present study, we investigated the first anti-HBV activity of a protein-enriched fraction (PE) from the larvae of the housefly (Musca domestica) in a stable HBV-producing cell line. HBsAg and HBeAg in the culture medium were measured by enzyme-linked immunosorbent assay. HBV-DNA was quantified by fluorescent quantification PCR. HBV core protein was assayed by immunofluorescent staining. Results indicate PE treatment inhibited both HBsAg, HBeAg secretion, and HBV-DNA replication. Furthermore, PE could also suppress HBV core protein expression. PE could be a potential candidate for the development of a novel and effective drug for the treatment of HBV infection.http://dx.doi.org/10.1155/2014/389560 |
spellingShingle | Xuemei Lu Xiaobao Jin Jie Wang Fujiang Chu Jiayong Zhu Antihepatitis B Virus Activity of a Protein-Enriched Fraction from Housefly (Musca domestica) in a Stable HBV-Producing Cell Line The Scientific World Journal |
title | Antihepatitis B Virus Activity of a Protein-Enriched Fraction from Housefly (Musca domestica) in a Stable HBV-Producing Cell Line |
title_full | Antihepatitis B Virus Activity of a Protein-Enriched Fraction from Housefly (Musca domestica) in a Stable HBV-Producing Cell Line |
title_fullStr | Antihepatitis B Virus Activity of a Protein-Enriched Fraction from Housefly (Musca domestica) in a Stable HBV-Producing Cell Line |
title_full_unstemmed | Antihepatitis B Virus Activity of a Protein-Enriched Fraction from Housefly (Musca domestica) in a Stable HBV-Producing Cell Line |
title_short | Antihepatitis B Virus Activity of a Protein-Enriched Fraction from Housefly (Musca domestica) in a Stable HBV-Producing Cell Line |
title_sort | antihepatitis b virus activity of a protein enriched fraction from housefly musca domestica in a stable hbv producing cell line |
url | http://dx.doi.org/10.1155/2014/389560 |
work_keys_str_mv | AT xuemeilu antihepatitisbvirusactivityofaproteinenrichedfractionfromhouseflymuscadomesticainastablehbvproducingcellline AT xiaobaojin antihepatitisbvirusactivityofaproteinenrichedfractionfromhouseflymuscadomesticainastablehbvproducingcellline AT jiewang antihepatitisbvirusactivityofaproteinenrichedfractionfromhouseflymuscadomesticainastablehbvproducingcellline AT fujiangchu antihepatitisbvirusactivityofaproteinenrichedfractionfromhouseflymuscadomesticainastablehbvproducingcellline AT jiayongzhu antihepatitisbvirusactivityofaproteinenrichedfractionfromhouseflymuscadomesticainastablehbvproducingcellline |