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Antiviral activity of the water extract and ethanol extract of against influenza A virus . | LitMetric

AI Article Synopsis

  • * Both extracts showed significant antiviral effects without being toxic to cells, inhibiting various stages of the influenza virus life cycle, including blocking viral entry and release.
  • * The extracts were found to impair key viral proteins, specifically hemagglutinin and neuraminidase, suggesting that SCH could be valuable for creating new antiviral drugs targeting influenza A viruses.

Article Abstract

Although vaccines and antivirals are currently available, influenza virus infections continually present major threats to human health. Due to genetic diversity and variability of influenza viruses, the development of new antiviral agents against the virus remains as a considerable challenge. In this study, we evaluated the antiviral activity of the water extract and ethanol extract of Hedl. (SCH), widely used as a medical herb, against influenza A viruses and identified molecular mechanisms for the antiviral activity. The water extract and ethanol extract of SCH demonstrated virucidal activity against influenza A virus at the noncytotoxic concentrations. In addition, cytopathic effect reduction assay and GFP fluorescence image analysis suggest that SCH extracts have inhibitory activity on multiple stages during influenza virus life cycle. Mechanisms studies showed that SCH extracts inhibited the biological functions of influenza viral surface hemagglutinin and neuraminidase proteins that play critical roles in the viral entry and release steps. SCH extracts not only prevented the receptor binding of influenza viral HA to the cellular receptors but also inhibited the HA-mediated membrane fusion. In addition, SCH extracts suppressed the enzyme activity of the viral neuraminidase. The results together suggest that SCH extracts contain antiviral natural compounds that inhibit multiple influenza viral proteins including the viral surface proteins. Our findings suggest that SCH extracts could be promising resources for the development of novel antiviral agents against influenza A viruses.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11620158PMC
http://dx.doi.org/10.1016/j.heliyon.2024.e39049DOI Listing

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