1. Academic Validation
  2. Ginsenoside Rb3 Suppresses Peste des Petits Ruminants Virus Replication by Inhibiting Autophagy to Potentiate Immune Responses

Ginsenoside Rb3 Suppresses Peste des Petits Ruminants Virus Replication by Inhibiting Autophagy to Potentiate Immune Responses

  • Microorganisms. 2026 Mar 26;14(4):738. doi: 10.3390/microorganisms14040738.
Qinglu Zhao 1 Hongmei Chen 1 Zhanying Hu 1 Dingcheng Wei 1 Xueliang Zhu 2 Rui Zhang 1
Affiliations

Affiliations

  • 1 Key Laboratory of Animal Medicine of Sichuan Education Department, Southwest Minzu University, Chengdu 610041, China.
  • 2 State Key Laboratory for Animal Disease Control and Prevention, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Xujiaping 1, Yanchangpu, Lanzhou 730046, China.
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 a morbillivirus in the family Paramyxoviridae. 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 Rb3, the major bioactive constituent in the Plants of ginseng, was reported to exert a wide range of pharmacologic and immunologic effects. However, it is unclear whether Ginsenoside Rb3 can act as an Antiviral against PPRV Infection. Here, we show that Ginsenoside Rb3 exhibits significant Antiviral activity against PPRV in Cell Culture models. The mechanism of action of Ginsenoside Rb3 against PPRV is mainly attributed to its ability to inhibit PPRV-mediated Autophagy, thus leading to promotion of interferon responses. In summary, our study establishes Ginsenoside Rb3 as a novel Antiviral agent effective against PPRV, sheds light on its mode of action, and reveals a novel immunomodulatory strategy that may prove essential for combating both current and future viral outbreaks.

Keywords

Peste des petits ruminants virus; antiviral; autophagy; ginsenoside Rb3; immunomodulatory strategy.

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