Cytokine storms and pyroptosis are primarily responsible for the rapid death of mice infected with pseudorabies virus
Author(s) -
Wei Sun,
Shanshan Liu,
Xuefei Huang,
Rui Yuan,
Jiansheng Yu
Publication year - 2021
Publication title -
royal society open science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.84
H-Index - 51
ISSN - 2054-5703
DOI - 10.1098/rsos.210296
Subject(s) - pyroptosis , pathogenesis , pseudorabies , biology , virus , cytokine , cytokine storm , virology , immunology , caspase 1 , proinflammatory cytokine , inflammation , inflammasome , disease , medicine , pathology , infectious disease (medical specialty) , covid-19
Pseudorabies virus (PRV), the causative agent of Aujeszky's disease, is one of the most harmful pathogens to the pig industry. PRV can infect and kill a variety of mammals. Nevertheless, the underlying pathogenesis related to PRV is still unclear. This study aims to investigate the pathogenesis induced by PRV in a mouse model. The mice infected with the PRV-HLJ strain developed severe clinical manifestations at 36 h post-infection (hpi), and mortality occurred within 48–72 hpi. Hematoxylin-eosin staining and qRT-PCR methods were used to detect the pathological damage and expression of cytokines related to an immune reaction in brain tissue, respectively. The cytokine storms caused by IFN-α, IFN- β , TNF-α, IL-1 β , IL-6 and IL-18 were related to the histopathological changes induced by PRV. This pattern of cytokine secretion depicts an image of typical cytokine storms, characterized by dysregulated secretion of pro-inflammatory cytokines and imbalanced pro-inflammatory and anti-inflammatory responses. In addition, the pyroptosis pathway was also activated by PRV by elevating the expression levels of nod-like receptor protein 3, Caspase-1, Gasdermin-D and interleukin-1 β /18. These findings provide a way for further understanding the molecular basis in PRV pathogenesis.
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