数字农科院2.0

Pathogen-derived peptidoglycan skeleton enhances innate immune defense against Staphylococcus aureus via mTOR-HIF-1α-HK2-mediated trained immunity

文献类型： 外文期刊

作者： Zheng Jia;Lingdi Niu;Junjie Guo;Jiaqing Wang;Hai Li;Runhang Liu;Ning Liu;Shuhe Zhang;Fang Wang;Junwei Ge

作者机构：

关键词： Innate immunity;Metabolic reprogramming;Methicillin-resistance;Peptidoglycan skeleton;Staphylococcus aureus;Trained immunity

期刊名称： Microbiological Research

ISSN： 0944-5013

年卷期： 2025 年 296 卷

页码：

收录情况： SCIE（2025版） ; ; EI（2025版）

摘要： Regulation of the innate immune response may be an effective strategy to enhance Staphylococcus aureus vaccines. Based on our previous findings that the Listeria peptidoglycan skeleton (pBLP) enhances the immune response through an unknown mechanism, we hypothesized that pBLP provides protection by modulating the innate immune response via trained immunity. In vitro, pBLP increased phagocytosis and inflammatory cytokine levels and elevated the anti-inflammatory cytokine TGF-β following secondary stimulation. In an in vivo model, our findings indicate that pBLP, when administered with a vaccine, protects mice from methicillin-resistant S. aureus challenge and also provides protection against S. aureus CMCC26003 in the absence of antigens. Using an ex vivo model, we demonstrated that pBLP increases markers of trained immunity in peritoneal macrophages. Transcriptome analysis of differentially expressed genes and inhibitor experiments revealed that the trained immunity process induced by pBLP depends on mTOR-HIF-1α and hexokinase 2. This study is the first to demonstrate that pBLP can induce trained immunity. Furthermore, we show that the peptidoglycan skeleton induces a distinct trained immunity phenotype compared to β-glucan, enhancing vaccine protection. Our study provides valuable insights for the design of novel vaccines that integrate both specific and innate immune responses.

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