@article{204556,
  author = {Ahn Jeong and Vikram Gopal and Aartjan Velthuis},
  title = {Zinc Ions Inactivate Influenza Virus Hemagglutinin and Prevent Receptor Binding},
  abstract = {<p><strong>Background:</strong> Influenza A viruses (IAV) cause seasonal flu and occasional pandemics. In addition, the potential for the emergence of new strains presents unknown challenges for public health. Face masks and other personal protective equipment (PPE) can act as barriers that prevent the spread of these viruses. Metal ions embedded into PPE have been demonstrated to inactivate respiratory viruses, but the underlying mechanism of inactivation and potential for resistance is presently not well understood. <strong>Methods:</strong> In this study, we used hemagglutination assays to quantify the effect of zinc ions on IAV sialic acid receptor binding. We varied the zinc concentration, incubation time, incubation temperature, and passaged IAV in the presence of zinc ions to investigate if resistance to zinc ions could evolve. <strong>Results:</strong> We found that zinc ions impact the ability of IAV particles to hemagglutinate and observed inhibition within 1 min of exposure. Maximum inhibition was achieved within 1 h and sustained for at least 24 h in a concentration-dependent manner. Inhibition was also temperature-dependent, and optimal above room temperature. Serial passaging of IAV in the presence of zinc ions did not result in resistance. <strong>Conclusions:</strong> e conclude that zinc ions prevent IAV hemagglutination in a concentration and temperature-dependent manner for at least 24 h. Overall, these findings are in line with previous observations indicating that zinc-embedded materials can inactivate the IAV hemagglutinin and SARS-CoV-2 spike proteins, and they support work toward developing robust, passive, self-cleaning antiviral barriers in PPE.</p>},
  year = {2025},
  journal = {Biomedicines},
  volume = {13},
  chapter = {1843},
  month = {07/2025},
  url = {https://www.mdpi.com/2227-9059/13/8/1843},
  doi = {10.3390/biomedicines13081843},
}