CSFV restricts necroptosis to sustain infection by inducing autophagy/mitophagy-targeted degradation of RIPK3

Microbiol Spectr. 2024 Jan 11;12(1):e0275823. doi: 10.1128/spectrum.02758-23. Epub 2023 Dec 15.

Abstract

CSFV infection in pigs causes persistent high fever, hemorrhagic necrotizing multi-organ inflammation, and high mortality, which seriously threatens the global swine industry. Cell death is an essential immune response of the host against pathogen invasion, and lymphopenia is the most typical clinical feature in the acute phase of CSFV infection, which affects the initial host antiviral immunity. As an "old" virus, CSFV has evolved mechanisms to evade host immune response after a long genetic evolution. Here, we show that necroptosis is a limiting host factor for CSFV infection and that CSFV-induced autophagy can subvert this host defense mechanism to promote its sustained replication. Our findings reveal a complex link between necroptosis and autophagy in the process of cell death, provide evidence supporting the important role for CSFV in counteracting host cell necrosis, and enrich our knowledge of pathogens that may subvert and evade this host defense.

Keywords: CSFV; NS4A; RIPK3; TRIM25; autophagic degradation; autophagy; mitophagy; necroptosis.

MeSH terms

  • Animals
  • Autophagy
  • Classical Swine Fever Virus* / physiology
  • Classical Swine Fever* / genetics
  • Mitophagy
  • Necroptosis
  • Signal Transduction
  • Swine