State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Department of Pediatric Dentistry, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
mBio. 2024 Oct 16;15(10):e0183924. doi: 10.1128/mbio.01839-24. Epub 2024 Sep 9.
Dental caries is associated with microbial dysbiosis caused by the excessive proliferation of in dental biofilms, where oxidative stress serves as the major stressor to microbial communities. The adaptability of to oxidative stress is a prerequisite for its proliferation and even for exerting its virulence. Protein acetylation is a reversible and conserved regulatory mechanism enabling bacteria to rapidly respond to external environmental stressors. However, the functions of protein acetylation in regulating oxidative stress adaptability of are still unknown. Here, we unveil the impact of acetyltransferase ActA-mediated acetylation on regulating the oxidative stress response of overexpression increased the sensitivity of to hydrogen peroxide and diminished its competitive ability against . In contrast, deletion enhanced oxidative stress tolerance and competitiveness of . The mass spectrometric analysis identified pyruvate kinase (PykF) as a substrate of ActA, with its acetylation impairing its enzymatic activity and reducing pyruvate production. Supplementation with exogenous pyruvate mitigated oxidative stress sensitivity and restored competitiveness in multi-species biofilms. acetylation analysis further confirmed that ActA directly acetylates PykF, negatively affecting its enzymatic activity. Moreover, 18 potential lysine-acetylated sites on PykF were identified , which account for 75% of lysine-acetylated sites detected . Taken together, our study elucidates a novel regulatory mechanism of ActA-mediated acetylation of PykF in modulating oxidative stress adaptability of by influencing pyruvate production, providing insights into the importance of protein acetylation in microbial environmental adaptability and interspecies interactions within dental biofilms.
Dental caries poses a significant challenge to global oral health, driven by microbial dysbiosis within dental biofilms. The pathogenicity of , a major cariogenic bacterium, is closely linked to its ability to adapt to changing environments and cellular stresses. Our investigation into the protein acetylation mechanisms, particularly through the acetyltransferase ActA, reveals a critical pathway by which modulates its adaptability to oxidative stress, the dominant stressor within dental biofilms. By elucidating how ActA affects the oxidative stress adaptability and competitiveness of through the regulatory axis of ActA-PykF-pyruvate, our findings provide insights into the dynamic interplay between cariogenic and commensal bacteria within dental biofilms. This work emphasizes the significance of protein acetylation in bacterial stress response and competitiveness, opening avenues for the development of novel strategies to maintain oral microbial balance within dental biofilms.
龋齿与微生物群落失调有关,这是由牙菌斑中 过度增殖引起的,其中氧化应激是微生物群落的主要应激源。 对氧化应激的适应性是其增殖甚至发挥其毒力的前提。蛋白质乙酰化是一种可逆且保守的调节机制,使细菌能够快速响应外部环境应激源。然而,蛋白质乙酰化在调节 氧化应激适应性中的功能尚不清楚。在这里,我们揭示了乙酰转移酶 ActA 介导的乙酰化对调节 过表达的氧化应激反应的影响,过表达增加了 对过氧化氢的敏感性,并降低了其与 的竞争力。相比之下, 缺失增强了 对氧化应激的耐受性和竞争力。质谱分析鉴定出丙酮酸激酶 (PykF) 是 ActA 的底物,其乙酰化会损害其酶活性并减少丙酮酸的产生。补充外源性丙酮酸可减轻氧化应激敏感性并恢复多物种生物膜中的竞争力。 ActA 乙酰化分析进一步证实,ActA 直接乙酰化 PykF,从而降低其酶活性。此外,在 PykF 上鉴定出 18 个潜在赖氨酸乙酰化位点,占检测到的赖氨酸乙酰化位点的 75%。总之,我们的研究阐明了 ActA 介导的 PykF 乙酰化在通过影响丙酮酸产生来调节 的氧化应激适应性方面的新型调节机制,为蛋白质乙酰化在微生物环境适应性和牙菌斑内种间相互作用中的重要性提供了新的认识。
龋齿对全球口腔健康构成重大挑战,其原因是牙菌斑内微生物群落失调。作为主要致龋菌的 ,其致病性与其适应不断变化的环境和细胞应激的能力密切相关。我们对蛋白质乙酰化机制的研究,特别是通过乙酰转移酶 ActA,揭示了 调节其对牙菌斑内主要应激源氧化应激的适应性的关键途径。通过阐明 ActA 通过 ActA-PykF-丙酮酸调节轴如何影响 的氧化应激适应性和竞争力,我们的发现揭示了牙菌斑内致龋菌和共生菌之间动态相互作用。这项工作强调了蛋白质乙酰化在细菌应激反应和竞争力中的重要性,为在牙菌斑内维持口腔微生物平衡开发新的策略开辟了途径。