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猪链球菌 2 型血清型 4 型分泌效应蛋白 SspA-1 通过 TLR2 内体和 I 型干扰素信号诱导前炎性细胞因子产生。

Streptococcus suis Serotype 2 Type IV Secretion Effector SspA-1 Induces Proinflammatory Cytokine Production via TLR2 Endosomal and Type I Interferon Signaling.

机构信息

Department of Breast and Thyroid Surgery, Chongqing General Hospital, Chongqing, China.

Department of Microbiology, College of Basic Medical Sciences, Key Laboratory of Microbial Engineering Under the Educational Committee in Chongqing, Army Medical University, Chongqing, China.

出版信息

J Infect Dis. 2024 Jul 25;230(1):188-197. doi: 10.1093/infdis/jiad454.

Abstract

The subtilisin-like protease-1 (SspA-1) plays an important role in the pathogenesis of a highly virulent strain of Streptococcus suis 2. However, the mechanism of SspA-1-triggered excessive inflammatory response is still unknown. In this study, we demonstrated that activation of type I IFN signaling is required for SspA-1-induced excessive proinflammatory cytokine production. Further experiments showed that the TLR2 endosomal pathway mediates SspA-1-induced type I IFN signaling and the inflammatory response. Finally, we mapped the major signaling components of the related pathway and found that the TIR adaptor proteins Mal, TRAM, and MyD88 and the downstream activation of IRF1 and IRF7 were involved in this pathway. These results explain the molecular mechanism by which SspA-1 triggers an excessive inflammatory response and reveal a novel effect of type I IFN in S. suis 2 infection, possibly providing further insights into the pathogenesis of this highly virulent S. suis 2 strain.

摘要

枯草溶菌素蛋白酶 1(SspA-1)在高毒力猪链球菌 2 菌株的发病机制中发挥重要作用。然而,SspA-1 引发过度炎症反应的机制尚不清楚。在本研究中,我们证明了 I 型 IFN 信号的激活对于 SspA-1 诱导的过度促炎细胞因子产生是必需的。进一步的实验表明,TLR2 内体途径介导了 SspA-1 诱导的 I 型 IFN 信号和炎症反应。最后,我们定位了相关途径的主要信号成分,发现 TIR 衔接蛋白 Mal、TRAM 和 MyD88 以及下游 IRF1 和 IRF7 的激活参与了这一途径。这些结果解释了 SspA-1 引发过度炎症反应的分子机制,并揭示了 I 型 IFN 在猪链球菌 2 感染中的新作用,可能为该高毒力猪链球菌 2 菌株的发病机制提供了进一步的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18c9/11272045/ffebd2637206/jiad454f1.jpg

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