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Updated: May 28, 2026

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Early Viral Entry Assays for the Identification and Evaluation of Antiviral Compounds
Published on: October 29, 2015
Phellodendron amurense Leaf Extract Inhibits Rhabdovirus Infection by Targeting Early Stages of Viral Entry.
Su Yeon Kim1, Taek-Kyun Lee2, Tae-Jin Choi1
1Department of Microbiology, School of Marine and Fisheries Sciences, Pukyong National University, Busan 48513, Republic of Korea.
Pathogens (Basel, Switzerland)
|May 27, 2026
Summary
Phellodendron amurense leaf extract shows promise as a broad-spectrum antiviral. This plant extract effectively inhibits viral entry and infectivity in enveloped RNA viruses.
Area of Science:
- Virology
- Natural Product Chemistry
- Drug Discovery
Background:
- RNA viruses mutate rapidly, requiring antivirals targeting conserved infection pathways.
- Viral hemorrhagic septicemia virus (VHSV) serves as a safe surrogate for high-throughput screening of potential antiviral agents.
Purpose of the Study:
- To identify novel antiviral compounds from natural sources using VHSV as a model.
- To investigate the mechanism of action of promising antiviral candidates.
Main Methods:
- High-throughput screening of 17,265 compounds, 2000 plant extracts, and 100 marine extracts against a recombinant VHSV.
- Cytotoxicity and antiviral activity assays, including dose-response, virucidal assays, and time-of-addition experiments.
- Fractionation of active extracts and analysis of lipophilic compound involvement.
Main Results:
- Phellodendron amurense (PL) leaf extract demonstrated significant antiviral activity with low cytotoxicity (selectivity index ≈ 10).
- The PL extract reduced viral infectivity and showed cross-activity against snakehead rhabdovirus.
- Mechanistic studies indicated the extract acts at early infection stages, likely by inactivating viral particles and interfering with attachment/entry.
Conclusions:
- Phellodendron amurense leaf extract is a potent antiviral agent targeting conserved entry mechanisms in enveloped RNA viruses.
- Lipophilic compounds in the n-hexane fraction are likely responsible for the observed antiviral effects.
- This extract represents a promising source for developing broad-spectrum antivirals.
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