Graduate Program in Dentistry, Federal University of Rio Grande do Sul (UFRGS), Porto Alegre, Brazil.
Bioinformatics and Biostatistics Core Facility, Institute of Basic Health Sciences, Federal University of Rio Grande do Sul (UFRGS), Porto Alegre, Brazil.
Mol Oral Microbiol. 2024 Oct;39(5):393-406. doi: 10.1111/omi.12463. Epub 2024 Mar 28.
This study aimed to characterize the taxonomic composition of intraradicular multispecies biofilms (IMB) formed in situ in a model to reproduce clinical conditions. Twelve palatal roots of maxillary molars had its canals prepared. Two roots were randomly selected to sterility control. Ten intraoral prosthetic appliances with lateral slots were fabricated. The roots were positioned in the slots with the canal access open to the oral cavity. Eight volunteers wore the appliance for 21 days, and two wore it at two different time points. One root from each appliance was removed and stored at -20°C until DNA extraction and sequencing (n = 10). Biofilm was analyzed using next-generation sequencing and bioinformatics. The V4 hyper-variable region of the 16SrRNA gene was amplified and sequenced. For data analyses, the mothur pipeline was used for 16SrRNA processing, and subsequent analyses of the sequence dataset were performed in R using the Microbiome Analyst R package. The taxonomy-based analysis of bacterial communities identified 562 operational taxonomic units (OTUs), which belonged to 93 genera, 44 families, and 8 phyla. Bacterial colonization was different for each biofilm, and samples did not have the same group of bacteria. Alpha and beta diversity analysis revealed some general patterns of sample clustering. A core microbiome of prevalent OTUs and genera was identified. IMBs were heterogeneous when analyzed individually, but some diversity patterns were found after sample clustering. The experimental model seemed to reproduce the actual biofilm composition in endodontic infections, which suggests that it may be used to evaluate disinfection protocols.
本研究旨在对原位形成的根管内多物种生物膜(IMB)的分类组成进行特征分析,该模型用于复制临床条件。上颌磨牙的 12 个腭根进行了根管预备。随机选择两个根进行无菌对照。制作了 10 个带有侧槽的口腔内修复体。将根放入槽中,使根管开口通向口腔。8 名志愿者佩戴义齿 21 天,其中 2 名在不同时间点佩戴。从每个义齿中取出一根根并储存在-20°C,直到提取和测序 DNA(n=10)。使用下一代测序和生物信息学分析生物膜。扩增和测序 16SrRNA 基因的 V4 高变区。对于数据分析, mothur 管道用于 16SrRNA 处理,然后使用 Microbiome Analyst R 软件包在 R 中对序列数据集进行后续分析。基于分类的细菌群落分析确定了 562 个操作分类单元(OTU),它们属于 93 个属、44 个科和 8 个门。每种生物膜的细菌定植情况不同,并且样本没有相同的细菌群。alpha 和 beta 多样性分析揭示了样本聚类的一些一般模式。确定了一个常见 OTU 和属的核心微生物组。单独分析 IMB 时存在异质性,但在进行样本聚类后发现了一些多样性模式。实验模型似乎复制了牙髓感染中的实际生物膜组成,这表明它可能用于评估消毒方案。