Gerhard Nicolas, Thurnheer Thomas, Kreutzer Susanne, Gmür Rudolf Dominik, Attin Thomas, Russo Giancarlo, Karygianni Lamprini
Clinic for Conservative and Preventive Dentistry, Center of Dental Medicine, University of Zurich, Plattenstrasse 11, 8032 Zurich, Switzerland.
Functional Genomics Center Zurich, University of Zurich/ETH Zurich, 8057 Zurich, Switzerland.
Antibiotics (Basel). 2021 Oct 1;10(10):1197. doi: 10.3390/antibiotics10101197.
Necrotizing gingivitis (NG) is a necrotizing periodontal disease that differs from chronic gingivitis (CG). To date, both the microbiological causes and the involved host cytokine response of NG still remain unclear. Here, we investigated corresponding interdental plaque and serum samples from two groups of Chinese patients with CG (n = 21) or NG (n = 21). The microbiota were studied by 16S rRNA Illumina MiSeq sequencing of the microbial metagenome and by assessing quantitatively the abundance of the phylum , the genus and the species , , and using fluorescence in situ hybridization (FISH). With respect to the associated host response, the levels of 30 inflammatory mediators were quantified by multiplex immunoassay analysis. Differential microbial abundance analysis of the two disease groups revealed at the phylum level that accounted for 67% of the differentially abundant organisms, followed by organisms of (21%) and (9%). At the species level, significant differences in abundance were seen for 75 species of which 58 species were significantly more abundant in CG patients. Notably, the FISH analysis revealed that was the most prevalent phylum in NG. The multiplex cytokine assay showed significant quantitative differences between the disease groups for eight analytes (GM-CSF, G-CSF, IFN-α, IL-4, IL-13, TNF-α, MIG, and HGF). The G-CSF was found to be the most significantly increased inflammatory protein marker in NG. The next-generation sequencing (NGS) data supported the understanding of NG as a multi-microbial infection with distinct differences to CG in regard to the microbial composition.
坏死性龈炎(NG)是一种与慢性龈炎(CG)不同的坏死性牙周疾病。迄今为止,NG的微生物病因及相关的宿主细胞因子反应仍不清楚。在此,我们研究了两组中国CG患者(n = 21)和NG患者(n = 21)的相应牙间隙菌斑和血清样本。通过对微生物宏基因组进行16S rRNA Illumina MiSeq测序以及使用荧光原位杂交(FISH)定量评估门、属和种、、和的丰度来研究微生物群。关于相关的宿主反应,通过多重免疫测定分析对30种炎症介质的水平进行了定量。对两个疾病组的差异微生物丰度分析显示,在门水平上,占差异丰富生物体的67%,其次是门的生物体(21%)和门的生物体(9%)。在种水平上,75个物种的丰度存在显著差异,其中58个物种在CG患者中显著更丰富。值得注意的是,FISH分析显示是NG中最普遍的门。多重细胞因子测定显示,在八个分析物(GM-CSF、G-CSF、IFN-α、IL-4、IL-13、TNF-α、MIG和HGF)方面,疾病组之间存在显著的定量差异。发现G-CSF是NG中炎症蛋白标志物增加最显著的。下一代测序(NGS)数据支持将NG理解为一种多微生物感染,在微生物组成方面与CG有明显差异。