Qi Maozhen, Liu Jianguo, Jiang Qingran, Niu Hongyu, Wang Xinyu, Zhou Dong, Lin Pengfei, Chen Huatao, Wang Aihua, Jin Yaping
Key Laboratory of Animal Biotechnology of the Ministry of Agriculture, College of Veterinary Medicine, Northwest A&F University, Yangling, 712100, Shaanxi, China.
Department of Clinical Veterinary Medicine, College of Veterinary Medicine, Northwest A&F University, Yangling, 712100, Shaanxi, China.
Braz J Microbiol. 2021 Jun;52(2):939-952. doi: 10.1007/s42770-021-00422-5. Epub 2021 Jan 16.
Trueperella pyogenes (T. pyogenes) is a common opportunistic pathogen of many livestock and play an important regulation role during multibacterial infection and interaction with the host by its primary virulence factor pyolysin (PLO). The purpose of this study was to investigate the regulation role of PLO which serve as a combinational pathogen with lipopolysaccharide (LPS) during endometritis. In this study, the expression of bioactive recombinant PLO (rPLO) in a prokaryotic expression system and its purification are described. Moreover, we observed that rPLO inhibited the innate immune response triggered by LPS and that methyl-β-cyclodextrin (MBCD) abrogated this inhibitory effect in goat endometrium stromal cells (gESCs). Additionally, we show from pharmacological and genetic studies that rPLO-induced autophagy represses gene expression by inhibiting NLRP3 inflammasome activation. Importantly, this study reported that ATF6 serves as a primary regulator of the cellular inflammatory reaction to rPLO. Overall, these observations suggest that T. pyogenes PLO could create an immunosuppressive environment for other pathogens invasion by regulating cellular signaling pathways.
化脓隐秘杆菌是许多家畜常见的机会性病原菌,其主要毒力因子溶血素(PLO)在多菌感染及与宿主相互作用过程中发挥重要调节作用。本研究旨在探讨PLO作为与脂多糖(LPS)联合的病原菌在子宫内膜炎中所起的调节作用。本研究描述了生物活性重组PLO(rPLO)在原核表达系统中的表达及其纯化。此外,我们观察到rPLO抑制LPS触发的天然免疫反应,且甲基-β-环糊精(MBCD)可消除山羊子宫内膜基质细胞(gESCs)中的这种抑制作用。此外,我们从药理学和遗传学研究表明,rPLO诱导的自噬通过抑制NLRP3炎性小体激活来抑制基因表达。重要的是,本研究报道ATF6作为细胞对rPLO炎症反应的主要调节因子。总体而言,这些观察结果表明,化脓隐秘杆菌PLO可通过调节细胞信号通路为其他病原菌入侵创造免疫抑制环境。