Altaie Alaa Muayad, Venkatachalam Thenmozhi, Patil Kiran, Al-Marzooq Farah, Rawat Surendra Singh, Qabbani Ali Al, Alsaegh Mohammed Amjed, Samaranayake Lakshman P, Soliman Sameh S M, Hamoudi Rifat
Research Institute of Medical and Health Sciences, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.
Center of Excellence for Precision Medicine, Research Institute of Medical and Health Sciences, University of Sharjah, Sharjah P.O. Box 27272, United Arab Emirates.
Curr Res Microb Sci. 2025 Jul 21;9:100443. doi: 10.1016/j.crmicr.2025.100443. eCollection 2025.
Periapical abscesses, radicular cysts, and periapical granulomas are among the most frequently identified pathological lesions in the alveolar bone. Although many studies have investigated bacterial metagenomics in periapical abscesses, little is known about the genome mining of abundant bacteria in periapical lesions and its correlation to human transcriptome. This study aims to explore the enriched metabolic environment of periapical lesions associated with microbial diversity and their role in lesion progression. Bacterial DNA and human RNA were isolated from periapical lesions and healthy pulp tissue and sequenced using next-generation sequencing (NGS). The sequences of the most abundant bacteria were then analyzed to identify secondary metabolites, pathogenic proteins, and their associated metabolic pathways. The results revealed that was the predominant bacterium in periapical abscesses and radicular cysts, whereas was the most abundant in periapical granulomas. Integrated bacterial and human metabolic pathways indicated that the augmentation of similar pathways is important in lesions pathogenesis. In periapical abscesses, inflammatory response, humoral immune response, positive regulation of cell migration, and hemopoiesis were enriched. In radicular cysts, pathways linked to NABA matrisome associated, inflammatory response, immune response-regulating signaling pathway, neutrophil degranulation, and P73 pathway were enriched. Meanwhile, periapical granulomas exhibited significant enrichment of pathways related to response to bacterium, regulation of immune effector process, and positive regulation of cell migration. In conclusion, this study is the first to elucidate the interplay between microbial and human metabolic activity associated with inflammation in abscesses, apoptosis in cysts, and inflammatory regulation in granulomas. These findings have significant clinical implications for the early diagnosis, prevention, and treatment of periapical lesions.
根尖脓肿、根端囊肿和根尖肉芽肿是牙槽骨中最常见的病理病变。尽管许多研究已经调查了根尖脓肿中的细菌宏基因组学,但对于根尖病变中丰富细菌的基因组挖掘及其与人类转录组的相关性却知之甚少。本研究旨在探索与微生物多样性相关的根尖病变的富集代谢环境及其在病变进展中的作用。从根尖病变和健康牙髓组织中分离细菌DNA和人类RNA,并使用下一代测序(NGS)进行测序。然后分析最丰富细菌的序列,以鉴定次生代谢产物、致病蛋白及其相关代谢途径。结果显示,[具体细菌名称1]是根尖脓肿和根端囊肿中的优势菌,而[具体细菌名称2]在根尖肉芽肿中最为丰富。整合的细菌和人类代谢途径表明,相似途径的增强在病变发病机制中很重要。在根尖脓肿中,炎症反应、体液免疫反应、细胞迁移的正调控和造血作用得到富集。在根端囊肿中,与NABA基质体相关、炎症反应、免疫反应调节信号通路、中性粒细胞脱颗粒和P73途径相关的途径得到富集。同时,根尖肉芽肿表现出与细菌反应、免疫效应过程调节和细胞迁移正调控相关途径的显著富集。总之