不同龋期牙菌斑微生物组结构差异的宏基因组研究及龋诊断模型的构建。

IF 4.6 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-09-10 DOI:10.1128/msystems.00044-25
Lei Dong, Jiazhen Yang, Hui Wu, Yanfei Sun, Jiang Liu, Hao Yuan, Mingchao Wang, Yajie Dai, Fei Teng, Gongchao Jing, Fang Yang
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引用次数: 0

摘要

龋齿的发展是一个动态的过程;然而,在高分辨率下,对龋病不同阶段微生物差异的了解有限。为了研究不同龋病阶段微生物组谱的变化,本研究招募了30名儿童,其中包括15名龋活跃患者和15名无龋患者。从无龋受试者的颊表面采集菌斑样本,定义为自信健康(CH; n = 15)。对于龋齿活跃的个体,从非空化表面(定义为相对健康[RH], n = 15)、牙釉质龋齿(EC, n = 15)和牙本质龋齿样本(DC, n = 15)收集菌斑样本。通过2bRAD测序平台对上述样品进行测序,揭示各组微生物群落结构。我们发现不同龋病阶段的微生物群落结构存在显著差异。物种丰富度以CH组最高(P < 0.05), RH组次之,EC组次之,DC组最低,后3组间差异不显著(P < 0.05)。②CH组与DC组微生物结构差异最大,RH/EC组与DC组之间的距离次之,RH组与EC组之间的差异最小。第三,不同龋期的特定种类差异显著。因此,我们开发了一种基于神经网络的深度学习方法的诊断模型,用于诊断不同阶段的龋齿,AUC超过98%。这可能为了解龋病病理进展的病因因素提供方法学上的支持。龋齿的诊断和治疗对人类口腔健康至关重要。以往的研究主要集中在龋病和健康牙齿之间的微生物差异,但对龋病不同阶段的微生物差异了解不够。我们的研究结果可以高分辨率地了解龋病不同阶段的微生物差异,从而利用深度学习方法建立基于微生物的诊断模型来区分龋病状态,准确率超过98%。这可能为了解龋病病理进展的病因因素提供方法学上的支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metagenomic research on the structural difference of plaque microbiome from different caries stages and the construction of a caries diagnostic model.

Development of dental caries is a dynamic process; yet, there is limited knowledge on microbial differences at various stages of caries at higher resolution. To investigate the shifting microbiome profiles across different caries stages, 30 children were enrolled in this study, including 15 caries-active patients and 15 caries-free individuals. Plaque samples were collected from the buccal surface of caries-free subjects, defined as confident health (CH; n = 15). For caries-active individuals, plaque samples were collected from non-cavitated surfaces (defined as relative health [RH], n = 15), enamel caries (EC; n = 15), and dentin caries samples (DC; n = 15). All the above samples were sequenced through the 2bRAD sequencing platform to reveal the microbial community structures in each group. We identified significant differences in microbial community structures from different caries stages. First, the CH group showed the highest species richness (P < 0.05), and then followed by the RH and EC groups with lower richness, and the lowest richness was found in the DC group, yet no significant difference was found among the last three groups (P > 0.05). Second, the microbial structure exhibited the greatest difference between CH and DC groups, followed by the distance between RH/EC and DC groups, and the smallest difference was found between RH and EC groups. Third, specific species were found with a significant difference during the different caries stages. Therefore, we developed a diagnostic model using deep learning methods based on neural networks to diagnose different caries stages with an AUC of over 98%. This may provide methodological support for the understanding of the etiological factor in the pathological progression of dental caries.IMPORTANCEThe diagnosis and treatment of dental caries are crucial for human oral health. Previous studies have focused on the microbial differences between caries and healthy teeth, but there was not enough knowledge on the microbial differences at different stages of dental caries. Our findings could provide a high-resolution understanding of the microbial divergencies among different stages of dental caries and thus build microbial-based diagnostic models for differentiating dental caries status using deep learning methods with an accuracy of over 98%. This may provide methodological support for the understanding of the etiological factor in the pathological progression of dental caries.

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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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