Sep 13 – 15, 2026
University of Muenster (Castle)
Europe/Berlin timezone

NATURAL PRODUCTS FROM PLANT BIODIVERSITY AS A SOURCE OF ANTIVIRAL AND PRO-RESOLVING COMPOUNDS AGAINST INFLUENZA A VIRUS

Sep 14, 2026, 1:34 PM
1m
Basement

Basement

Poster presentation Antivirals and Vaccines Poster viewing

Speaker

José Hugo de Sousa Gomes (UKM, Institute fur Virologie)

Description

Influenza A virus (IAV) remains a major global health challenge due to its high genetic variability, limited therapeutic options, and the emergence of antiviral resistance. Natural products are a promising source of antiviral agents. However, their antiviral and immunomodulatory mechanisms remain poorly understood. In particular, their potential to promote the resolution of virus-induced inflammation remains largely unexplored. In this context, our group has investigated two Brazilian species, Terminalia glabrescens (Tg) and Terminalia phaeocarpa (Tp), in in vitro models of Zika virus (ZIKV) and SARS-CoV-2 infection. Their antiviral activity has been associated with distinct classes of secondary metabolites, including the terpene β-sitosterol from Tg, the ellagitannins 1-O-α-galloylpunicalagin and punicalagin, and the flavonoids quercitrin and afzelin isolated from Tp leaves. Based on these findings, we investigated whether these natural products also exhibit antiviral and pro-resolving activity against IAV. While no cytotoxicity was observed, antiviral assays demonstrated that all tested compounds significantly reduced IAV replication. Further studies are evaluating their antiviral potency and investigating their capacity to modulate virus-induced inflammatory responses as pro-resolving agents. Collectively, these findings highlight plant-derived compounds as promising antiviral agents for IAV therapy.

Keywords

Antiviral agents; Pro-resolving agents; Influenza A virus; Brazilian biodiversity

Registration ID INF26-69
Professional status of the speaker Postdoc
Junior scientist status No, I am not a junior scientist.

Author

José Hugo de Sousa Gomes (UKM, Institute fur Virologie)

Co-authors

Dr Felipe Rocha da Silva Santos (UFMG) Dr Fernão Castro Braga (UFMG) Dr Eike R. Hrincius (UKM) Prof. Stephan Ludwig (UKM)

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