Deoxyshikonin Inhibits Influenza A Virus Infection at an Early Stage

Deoxyshikonin (DS) is a derivative of shikonin, the main compound present in <i>Lithospermi radi</i>, the root of <i>Lithospermum erythrorhizon</i> Siebold and Zucc. In this study, we investigated the antiviral effects of DS using Influenza A/PR8/34, which expresses green fluorescent protein (GFP) as well as wild-type PR8/34 H1N1 Influenza A virus (IAV). Fluorescence microscopy and flow cytometry results showed that DS from 1.25 to 5 µM significantly and dose-dependently inhibited PR8-GFP IAV infection. A plaque assay confirmed the inhibitory effect of DS against H1N1 IAV infection. Consistently, immunofluorescence results showed that DS suppresses IAV protein expression. Time-of-drug-addition and hemagglutination inhibition assays revealed that DS exhibits anti-influenza virus efficacy by blocking the viral attachment and penetration into the cells and has a direct virus-eradication effect in the early stages of infection. However, DS did not repress neuraminidase activity. Our findings suggest that DS could be used not only to protect against the early stages of IAV infection, but also to treat influenza virus infections in combination with NA inhibitors.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-08-22
DOI
https://doi.org/10.3390/ijms26178158
Primary Topic
Influenza Virus Research Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Deoxyshikonin Inhibits Influenza A Virus Infection at an Early Stage

Jin Yeul, Won‐Kyung Cho
International Journal of Molecular Sciences
Influenza Virus Research Studies
article

Deoxyshikonin Inhibits Influenza A Virus Infection at an Early Stage

Jin Yeul, Won‐Kyung Cho
article en

Abstract

Deoxyshikonin (DS) is a derivative of shikonin, the main compound present in <i>Lithospermi radi</i>, the root of <i>Lithospermum erythrorhizon</i> Siebold and Zucc. In this study, we investigated the antiviral effects of DS using Influenza A/PR8/34, which expresses green fluorescent protein (GFP) as well as wild-type PR8/34 H1N1 Influenza A virus (IAV). Fluorescence microscopy and flow cytometry results showed that DS from 1.25 to 5 µM significantly and dose-dependently inhibited PR8-GFP IAV infection. A plaque assay confirmed the inhibitory effect of DS against H1N1 IAV infection. Consistently, immunofluorescence results showed that DS suppresses IAV protein expression. Time-of-drug-addition and hemagglutination inhibition assays revealed that DS exhibits anti-influenza virus efficacy by blocking the viral attachment and penetration into the cells and has a direct virus-eradication effect in the early stages of infection. However, DS did not repress neuraminidase activity. Our findings suggest that DS could be used not only to protect against the early stages of IAV infection, but also to treat influenza virus infections in combination with NA inhibitors.

International Journal of Molecular SciencesVol. 26(17)
Korea Institute of Oriental Medicine (KR)
National Research Foundation, National Research Foundation Singapore, Chungnam National University, National Research Foundation of Korea, Ministry of Science and ICT, South Korea
Openalex Percentile: Top 70%
Influenza Virus Research Studies
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