Department of Periodontics, University of Washington, Seattle, WA, USA.
Department of Periodontics, University of Texas Health Science Center, San Antonio, TX, USA.
Mol Oral Microbiol. 2021 Feb;36(1):37-49. doi: 10.1111/omi.12323. Epub 2020 Dec 3.
Developing a laboratory model of oral polymicrobial communities is essential for in vitro studies of the transition from healthy to diseased oral plaque. SHI medium is an enriched growth medium capable of supporting in vitro biofilms with similar diversity to healthy supragingival inocula; however, this medium does not maintain the diversity of gram-negative bacteria more associated with subgingival plaque. Here, we systematically modified SHI medium components to investigate the impacts of varying nutrients and develop a medium capable of supporting a specific disease-state subgingival community. A diseased subgingival plaque sample was inoculated in SHI medium with increasing concentrations of sucrose (0%, 0.1%, 0.5%), fetal bovine serum (FBS) (0%, 10%, 20%, 30%, 50%), and mucin (0.1, 2.5, 8.0 g/L) and grown for 48 hrs, then the 16S rRNA profiles of the resulting biofilms were examined. In total, these conditions were able to capture 89 of the 119 species and 43 of the 51 genera found in the subgingival inoculum. Interestingly, biofilms grown in high sucrose media, although dominated by acidogenic Firmicutes with a low final pH, contained several uncultured taxa from the genus Treponema, information that may aid culturing these periodontitis-associated fastidious organisms. Biofilms grown in a modified medium (here named subSHI-v1 medium) with 0.1% sucrose and 10% FBS had a high diversity closest to the inoculum and maintained greater proportions of many gram-negative species of interest from the subgingival periodontal pocket (including members of the genera Prevotella and Treponema, and the Candidate Phyla Radiation phylum Saccharibacteria), and therefore best represented the disease community.
开发口腔多微生物群落的实验室模型对于体外研究从健康口腔斑块向疾病状态的转变至关重要。SHI 培养基是一种丰富的生长培养基,能够支持与健康龈上接种物相似多样性的体外生物膜;然而,这种培养基不能维持与龈下斑块更相关的革兰氏阴性菌的多样性。在这里,我们系统地修改了 SHI 培养基成分,以研究改变营养物质的影响,并开发一种能够支持特定疾病状态龈下群落的培养基。将患病的龈下斑块样本接种到 SHI 培养基中,蔗糖浓度逐渐增加(0%、0.1%、0.5%)、胎牛血清(FBS)(0%、10%、20%、30%、50%)和粘蛋白(0.1、2.5、8.0 g/L),培养 48 小时,然后检查所得生物膜的 16S rRNA 图谱。总共,这些条件能够捕获龈下接种物中 119 个物种中的 89 个和 51 个属中的 43 个。有趣的是,在高蔗糖培养基中生长的生物膜,尽管由产酸Firmicutes 主导,最终 pH 值较低,但含有几个未培养的Treponema属分类群,这些信息可能有助于培养这些与牙周炎相关的难培养的生物体。在含有 0.1%蔗糖和 10%FBS 的改良培养基(命名为 subSHI-v1 培养基)中生长的生物膜具有与接种物最接近的高多样性,并保持了龈下牙周袋中许多感兴趣的革兰氏阴性物种的更大比例(包括 Prevotella 和 Treponema 属的成员,以及候选门辐射门 Saccharibacteria),因此最能代表疾病群落。