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Plant extracts from Cameroonian medicinal plants strongly inhibit hepatitis C virus infection in vitro. | LitMetric

Plant extracts from Cameroonian medicinal plants strongly inhibit hepatitis C virus infection in vitro.

Front Microbiol

Molecular and Cellular Virology, Center for Infection and Immunity of Lille, Inserm U1019 - CNRS UMR 8204, Institut de Biologie de Lille, Pasteur Institute of Lille, University of Lille Lille, France.

Published: June 2015

According to some recent studies, Cameroon is one of the sub-Saharan African countries most affected by hepatitis C, with low access to the standard therapy based on the combination of pegylated interferon and ribavirin. A first ethnobotanical survey, conducted in the Western region of Cameroon, reported the use of several medicinal plants in traditional medicine for the healing of liver-related disorders. Crude organic extracts of five plants surveyed were prepared and their effect against hepatitis C virus (HCV) infection investigated. The HCV JFH1 strain cell culture system HCVcc was used. The antiviral activity was quantified by immunofluorescent labeling of HCV E1 envelope protein at 30 h post-infection in the presence of the plant extracts. Active compounds were then tested in time course infection experiments. Dose-response and cellular toxicity assays were also determined. Three extracts, methanol extracts from roots of Trichilia dregeana, stems of Detarium microcarpum and leaves of Phragmanthera capitata, showed anti-HCV activity, with half-maximal inhibitory concentration of 16.16, 1.42, and 13.17 μg/mL, respectively. Huh-7 cells were incubated with the extracts for 72 h and it appears that T. dregeana extract is not toxic up to 200 μg/mL, D. microcarpum up to 100 μg/mL and P. capitata up to 800 μg/mL. All the three extracts showed a strong inhibition of HCV entry and no effect on replication or secretion. Taken together, these results showed that extracts from Cameroonian medicinal plants are promising sources of anti-HCV agents.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4432692PMC
http://dx.doi.org/10.3389/fmicb.2015.00488DOI Listing

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