Wang Guizhen, Gao Yawen, Wu Xiuhua, Gao Xiue, Zhang Min, Liu Hongmei, Fang Tianqi
Department of Respiratory Medicine, The First Hospital of Jilin University, Jilin University, Changchun, China.
College of Food Engineering, Jilin Engineering Normal University, Changchun, China.
Front Microbiol. 2020 Nov 27;11:593588. doi: 10.3389/fmicb.2020.593588. eCollection 2020.
Suilysin (SLY) plays a critical role in infections making it an ideal target to the combat infection caused by this pathogen. In the present study, we found that piceatannol (PN), a natural compound, inhibits pore-formation by blocking the oligomerization of SLY without affecting the growth of and the expression of SLY. Furthermore, PN alleviated the J774 cell damage and the expression of the inflammatory cytokine tumor necrosis factor-α (TNF-α) and interleukin-1α (IL-1β) induced by . The computational biology and biochemistry results indicated that PN binds to the joint region of D2 and D4 in SLY, and Asn57, Pro58, Pro59, Glu76, Ile379, Glu380, and Glu418 were critical residues involved in the binding. The binding effect between PN and SLY hindered the SLY monomers from forming the oligomers, thereby weakening the hemolytic activity of SLY. This mechanism was also verified by hemolysis analysis and analysis of formation after site-specific mutagenesis. Furthermore, PN protected mice from infections by reducing bacterial colony formation and the inflammatory response in target organs . These results indicate that PN is a feasible drug candidate to combat infections.
溶细胞素(SLY)在感染过程中起关键作用,使其成为对抗该病原体引起的感染的理想靶点。在本研究中,我们发现天然化合物白皮杉醇(PN)通过阻断SLY的寡聚化来抑制孔形成,而不影响该病原体的生长和SLY的表达。此外,PN减轻了该病原体诱导的J774细胞损伤以及炎性细胞因子肿瘤坏死因子-α(TNF-α)和白细胞介素-1α(IL-1β)的表达。计算生物学和生物化学结果表明,PN与SLY中D2和D4的连接区域结合,天冬酰胺57、脯氨酸58、脯氨酸59、谷氨酸76、异亮氨酸379、谷氨酸380和谷氨酸418是参与该结合的关键残基。PN与SLY之间的结合作用阻碍了SLY单体形成寡聚物,从而削弱了SLY的溶血活性。位点特异性诱变后的溶血分析和孔形成分析也验证了这一机制。此外,PN通过减少细菌集落形成和靶器官中的炎症反应来保护小鼠免受该病原体感染。这些结果表明,PN是对抗该病原体感染的一种可行的候选药物。