Systems Biology of Complex Diseases, Translational Health Research Center (CENITRES), Maimónides University, Buenos Aires, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina; Faculty of Health Science, Maimónides University, Buenos Aires, Argentina.
Max Planck Institute for Immunobiology and Epigenetics, Bioinformatics Facility, Germany.
EBioMedicine. 2024 Mar;101:104996. doi: 10.1016/j.ebiom.2024.104996. Epub 2024 Feb 5.
The pathogenesis of MASLD (metabolic dysfunction-associated steatotic liver disease), including its severe clinical forms, involves complex processes at all levels of biological organization. This study examined the potential link between the liver microbiome profile and epigenetic factors.
Liver microbial DNA composition was analysed using high throughput 16S rRNA gene sequencing in 116 individuals, with 55% being female, across the spectrum of liver disease severity. Total activity of histone deacetylases (HDACs) and acetyltransferases (HATs) was assayed in nuclear extracts from fresh liver samples. In addition, we measured the global 5-hydroxymethylcytosine (5-hmC) levels of liver DNA.
Patients with MASLD showed a 2.07-fold increase (p = 0.013) in liver total HAT activity. Moreover, a correlation was observed between liver total HAT activity and the score for histological steatosis (Spearman's R = 0.60, p = 1.0E-3) and disease severity (R = 0.40, p = 2.0E-2). Liver HAT and HDAC activities also showed associations with the abundance of several liver bacterial DNAs. Additionally, liver global levels of 5-hmC showed negative correlation with the read number of Bacteroidetes (R = -0.62, p = 9.3E-4) and Gammaproteobacteria (R = -0.43, p = 3.2E-2), while it was positively correlated with the abundance of Acidobacteria (R = 0.42, p = 4.1E-2) and Actinobacteria (R = 0.47, p = 1.8E-2).
The host liver epigenome, including the activity of enzymes involved in maintaining the balance between protein acetylation and deacetylation and the global DNA hydroxy-methylation status, may be the target of microbial signals.
Agencia Nacional de Promoción Científica y Tecnológica, FonCyT.
MASLD(代谢相关脂肪性肝病)的发病机制,包括其严重的临床形式,涉及生物组织各级别的复杂过程。本研究探讨了肝微生物组谱与表观遗传因素之间的潜在联系。
采用高通量 16S rRNA 基因测序技术分析了 116 名个体的肝微生物 DNA 组成,其中 55%为女性,涵盖了肝病严重程度的各个范围。从新鲜肝组织样本的核提取物中测定组蛋白去乙酰化酶(HDACs)和乙酰转移酶(HATs)的总活性。此外,我们还测量了肝 DNA 的全基因组 5-羟甲基胞嘧啶(5-hmC)水平。
MASLD 患者的肝总 HAT 活性增加了 2.07 倍(p=0.013)。此外,肝总 HAT 活性与组织学脂肪变性评分(Spearman's R=0.60,p=1.0E-3)和疾病严重程度(R=0.40,p=2.0E-2)之间存在相关性。肝 HAT 和 HDAC 活性也与几种肝细菌 DNA 的丰度相关。此外,肝全基因组 5-hmC 水平与拟杆菌门(R=-0.62,p=9.3E-4)和γ变形菌门(R=-0.43,p=3.2E-2)的读取数呈负相关,而与酸杆菌门(R=0.42,p=4.1E-2)和放线菌门(R=0.47,p=1.8E-2)的丰度呈正相关。
宿主肝表观基因组,包括参与维持蛋白质乙酰化和去乙酰化平衡的酶的活性以及全基因组 DNA 羟甲基化状态,可能是微生物信号的靶点。
阿根廷国家科学技术促进署,FONCyT。