NLRP3 inflammasome in major swine viral infections: Host defense and viral antagonism

The NLRP3 inflammasome is a cytosolic signaling platform that drives caspase-1-dependent maturation of IL-1β and IL-18 and gasdermin D (GSDMD)-mediated pyroptosis. During infection with major porcine viruses – including African swine fever virus, porcine reproductive and respiratory syndrome virus, pseudorabies virus, porcine epidemic diarrhea virus, transmissible gastroenteritis virus, and porcine circovirus type 2, NLRP3 exerts opposing effects: moderate activation restricts viral propagation, whereas sustained stimulation drives tissue injury. We review how structurally unrelated viral proteins converge on limited upstream events – endolysosomal damage, ion flux, mitochondrial injury, ER stress, and the ubiquitin–autophagy network. Because genetically distinct porcine pathogens exploit this same regulatory axis, it represents a shared point of vulnerability. We assess therapeutic options targeting NLRP3 assembly, GSDMD pore formation, and host proteostasis, and highlight questions requiring validation in porcine cells and pigs.

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Publication Details

Journal
Figshare
Published
2026-10-30
DOI
https://doi.org/10.6084/m9.figshare.34865469
Primary Topic
Inflammasome and immune disorders
Type
article
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article

NLRP3 inflammasome in major swine viral infections: Host defense and viral antagonism

Ya-di Guo, Sheng‐Li Ming, Bei‐Bei Chu, Yu-Xin Xiang et al.
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Figshare
Inflammasome and immune disorders
article

NLRP3 inflammasome in major swine viral infections: Host defense and viral antagonism

Ya-di Guo, Sheng‐Li Ming, Bei‐Bei Chu, Yu-Xin Xiang, Hang-Tian Mei, Jiang Wang, Guo-Yu Yang, Ying-Nan Li, Lei Zeng, Yang Wang
article en

Abstract

The NLRP3 inflammasome is a cytosolic signaling platform that drives caspase-1-dependent maturation of IL-1β and IL-18 and gasdermin D (GSDMD)-mediated pyroptosis. During infection with major porcine viruses – including African swine fever virus, porcine reproductive and respiratory syndrome virus, pseudorabies virus, porcine epidemic diarrhea virus, transmissible gastroenteritis virus, and porcine circovirus type 2, NLRP3 exerts opposing effects: moderate activation restricts viral propagation, whereas sustained stimulation drives tissue injury. We review how structurally unrelated viral proteins converge on limited upstream events – endolysosomal damage, ion flux, mitochondrial injury, ER stress, and the ubiquitin–autophagy network. Because genetically distinct porcine pathogens exploit this same regulatory axis, it represents a shared point of vulnerability. We assess therapeutic options targeting NLRP3 assembly, GSDMD pore formation, and host proteostasis, and highlight questions requiring validation in porcine cells and pigs.

Figshare
Good health and well-being
Openalex Percentile: Top 22%
Inflammasome and immune disorders
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