Mineralo-organic particles inhibit influenza A virus infection by targeting viral hemagglutinin activity

Aim: Mineralo-organic particles, naturally present in human body fluids, participate in ectopic calcification and inflammatory diseases. These particles coexist with influenza A virus (IAV) in the same microenvironment during viral infection. Our objective was to investigate the functional consequen...

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Hauptverfasser: Chiang, Huan-Jung, Peng, Hsin-Hsin, Weng, Kuo-Feng, Hsiung, Kuei-Ching, Liang, Chieh-Yu, Kuo, Shun-Li, Ojcius, David M., Young, John Ding-E, Shih, Shin-Ru
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Sprache:eng
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Zusammenfassung:Aim: Mineralo-organic particles, naturally present in human body fluids, participate in ectopic calcification and inflammatory diseases. These particles coexist with influenza A virus (IAV) in the same microenvironment during viral infection. Our objective was to investigate the functional consequences of the potential interactions between these particles and the virions. Materials & methods: We used in vitro models, including electron microscopy, fluorescence microscopy, hemagglutination assay and viral infection assays to examine the interactions. Results: Mineralo-organic particles bind to IAV virions through interactions involving particle-bound fetuin-A and mineral content, effectively engaging viral hemagglutinin. These interactions result in hindered viral infection. Conclusion: These findings uncover the novel interactions between mineralo-organic particles and IAV, highlighting the impact of virus microenvironment complexity. In vitro mineralo-organic particles, produced in controlled settings, enabled study of particle−virion interactions with physiological implications. These particles are capable of binding to influenza A virus and reduce infection in mammalian cells. Mineralo-organic particles exhibit the ability to inhibit influenza A virus-induced hemagglutination and disrupt viral attachment to cells by engaging in interactions between particle-associated fetuin-A and viral HA. Mineralo-organic particles are capable of engaging with virions, thereby presenting a particle-mediated host factor that influences infectious disease outcomes.
DOI:10.6084/m9.figshare.27102904