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Middle East respiratory syndrome coronavirus infection is inhibited by griffithsin

Abstract : Highly pathogenic human coronaviruses associated with a severe respiratory syndrome, including Middle East respiratory syndrome coronavirus (MERS-CoV), have recently emerged. The MERS-CoV epidemic started in 2012 and is still ongoing, with a mortality rate of approximately 35%. No vaccine is available against MERS-CoV and therapeutic options for MERS-CoV infections are limited to palliative and supportive care. A search for specific antiviral treatments is urgently needed. Coronaviruses are enveloped viruses, with the spike proteins present on their surface responsible for virus entry into the target cell. Lectins are attractive anti-coronavirus candidates because of the highly glycosylated nature of the spike protein. We tested the antiviral effect of griffithsin (GRFT), a lectin isolated from the red marine alga Griffithsia sp. against MERS-CoV infection. Our results demonstrate that while displaying no significant cytotoxicity, griffithsin is a potent inhibitor of MERS-CoV infection. Griffithsin also inhibits entry into host cells of particles pseudotyped with the MERS-CoV spike protein, suggesting that griffithsin inhibits spike protein function during entry. Spike proteins have a dual function during entry, they mediate binding to the host cell surface and also the fusion of the viral envelope with host cell membrane. Time course experiments show that griffithsin inhibits MERS-CoV infection at the binding step. In conclusion, we identify griffithsin as a potent inhibitor of MERS-CoV infection at the entry step.
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Contributor : Karin Séron Connect in order to contact the contributor
Submitted on : Friday, April 19, 2019 - 3:14:00 PM
Last modification on : Wednesday, November 3, 2021 - 4:36:05 AM

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Jean K. Millet, Karin Séron, Rachael Labitt, Adeline Danneels, Kenneth Palmer, et al.. Middle East respiratory syndrome coronavirus infection is inhibited by griffithsin. Antiviral Research, Elsevier Masson, 2016, 133, pp.1-8. ⟨10.1016/j.antiviral.2016.07.011⟩. ⟨hal-02104470⟩



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