Department of Oral Immunology and Infectious Diseases, School of Dentistry, University of Louisville, Louisville, KY, United States.
Complex Carbohydrate Research Center, University of Georgia, Athens, GA, United States.
Front Cell Infect Microbiol. 2024 Jun 12;14:1418651. doi: 10.3389/fcimb.2024.1418651. eCollection 2024.
This study unveils the intricate functional association between cyclic di-3',5'-adenylic acid (c-di-AMP) signaling, cellular bioenergetics, and the regulation of lipopolysaccharide (LPS) profile in , a Gram-negative obligate anaerobe considered as a keystone pathogen involved in the pathogenesis of chronic periodontitis. Previous research has identified variations in LPS profile as a major virulence factor, yet the underlying mechanism of its modulation has remained elusive.
We employed a comprehensive methodological approach, combining two mutants exhibiting varying levels of c-di-AMP compared to the wild type, alongside an optimized analytical methodology that combines conventional mass spectrometry techniques with a novel approach known as FLAT.
We demonstrate that c-di-AMP acts as a metabolic nexus, connecting bioenergetic status to nuanced shifts in fatty acid and glycosyl profiles within LPS. Notably, the predicted regulator gene , serving as a potent regulator of c-di-AMP synthesis, was found essential for producing N-acetylgalactosamine and an unidentified glycolipid class associated with the LPS profile.
The multifaceted roles of c-di-AMP in bacterial physiology are underscored, emphasizing its significance in orchestrating adaptive responses to stimuli. Furthermore, our findings illuminate the significance of LPS variations and c-di-AMP signaling in determining the biological activities and immunostimulatory potential of LPS, promoting a pathoadaptive strategy. The study expands the understanding of c-di-AMP pathways in Gram-negative species, laying a foundation for future investigations into the mechanisms governing variations in LPS structure at the molecular level and their implications for host-pathogen interactions.
本研究揭示了环状二核苷酸(c-di-AMP)信号、细胞生物能学与脂多糖(LPS)谱调控之间复杂的功能关联,这种关联在被认为是参与慢性牙周炎发病机制的关键病原体的革兰氏阴性专性厌氧菌 中存在。先前的研究已经确定 LPS 谱的变异是主要的毒力因子,但调节其的潜在机制仍不清楚。
我们采用了一种综合的方法学方法,结合了两种与野生型相比表现出不同 c-di-AMP 水平的突变体,以及一种结合了常规质谱技术和一种称为 FLAT 的新方法的优化分析方法。
我们证明 c-di-AMP 作为代谢枢纽,将生物能状态与 LPS 内脂肪酸和糖基谱的细微变化联系起来。值得注意的是,作为 c-di-AMP 合成的有力调节剂的预测调控基因 ,对于产生与 LPS 谱相关的 N-乙酰半乳糖胺和一种未鉴定的糖脂类是必不可少的。
c-di-AMP 在细菌生理学中的多方面作用得到了强调,强调了它在协调对刺激的适应性反应中的重要性。此外,我们的发现阐明了 LPS 变异和 c-di-AMP 信号在决定 LPS 生物学活性和免疫刺激潜力中的重要性,促进了一种病理适应策略。该研究扩展了对革兰氏阴性物种中 c-di-AMP 途径的理解,为未来在分子水平上研究 LPS 结构变异的机制及其对宿主-病原体相互作用的影响奠定了基础。