Ginsenoside Rh1 suppresses Peste des petits ruminants virus replication by inhibiting autophagy to promote interferon responses and restrict inflammatory responses.

Abstract

Peste des Petits Ruminants (PPR), a highly contagious disease of domestic and wild small ruminants, is characterized by severe morbidity and mortality. PPRV, the causative agent, is ain the family. The virus poses a significant barrier to sustainable agricultural development in the developing world. Currently, no effective therapeutics agent for PPRV infection is available. Ginsenoside Rh1, a protopanaxadiol ginsenoside, the major pharmacological ingredient in the plants of ginseng, was reported to inhibit the replication of a broad range of human viruses. However, it is unclear whether Ginsenoside Rh1 can act as an antiviral against PPRV infection. Here, we demonstrate that Ginsenoside Rh1 exhibits significant antiviral activity against PPRV in cell culture models. The mechanism of action of Ginsenoside Rh1 against PPRV is mainly attributed to its ability to block PPRV mediated autophagy, thus leading to stimulation of interferon responses and inhibition of inflammatory responses. In summary, our study establishes Ginsenoside Rh1 as a novel antiviral agent effective against PPRV and potentially other related morbilliviruses, sheds light on its mode of action, and reveals a novel autophagy-dependent dual immunomodulatory strategy that may prove essential for combating both current and future viral outbreaks.