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通过纳米孔测序对口腔微生物组进行宏基因组分析揭示了与健康儿童相比,患有磨牙切牙矿化不全(MIH)的患者微生物组的结构差异——病例研究。

Metagenomic Analysis of the Buccal Microbiome by Nanopore Sequencing Reveals Structural Differences in the Microbiome of a Patient with Molar Incisor Hypomineralization (MIH) Compared to a Healthy Child-Case Study.

作者信息

Tynior Wojciech, Kłósek Małgorzata, Salatino Silvia, Cuber Piotr, Hudy Dorota, Nałęcz Dariusz, Chan Yuen-Ting, Gustave Carla, Strzelczyk Joanna Katarzyna

机构信息

Department of Medical and Molecular Biology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia in Katowice, 19 Jordana St., 41-808 Zabrze, Poland.

Department of Microbiology and Immunology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia in Katowice, 19 Jordana St., 41-808 Zabrze, Poland.

出版信息

Int J Mol Sci. 2024 Dec 6;25(23):13143. doi: 10.3390/ijms252313143.

Abstract

Molar incisor hypomineralization (MIH) is a qualitative developmental defect that affects the enamel tissue of permanent molars and can also occur in permanent incisors. Enamel affected by MIH has reduced hardness, increased porosity, and a higher organic content than unaffected enamel. These characteristics predispose the enamel to accumulation of bacteria and a higher prevalence of caries lesions. Through a groundbreaking metagenomic analysis of the buccal mucosal sample from a patient with MIH, we explored the intricacies of its microbiome compared to a healthy control using state-of-the-art nanopore long-read sequencing. Out of the 210 bacterial taxa identified in the MIH microbiome, we found and to be the most abundant genera. The bacteria with the highest read counts in the patient with MIH included , , , , and . Our results revealed a striking contrast between healthy and MIH affected children, with a higher dominance and number of pathogenic species (, , and ) and reduced diversity in the MIH-affected patient. This distinct microbial profile not only sheds light on MIH-affected patients, but paves the way for future research, inspiring deeper understanding and larger scale studies.

摘要

磨牙症伴切牙矿化不全(MIH)是一种影响恒牙磨牙釉质组织的质性发育缺陷,也可能发生在恒切牙。受MIH影响的釉质硬度降低、孔隙率增加,且有机质含量高于未受影响的釉质。这些特征使釉质更容易积累细菌,患龋损的几率更高。通过对一名MIH患者的颊黏膜样本进行开创性的宏基因组分析,我们使用最先进的纳米孔长读长测序技术,与健康对照相比,探索了其微生物组的复杂性。在MIH微生物组中鉴定出的210个细菌分类群中,我们发现[具体属名1]和[具体属名2]是最丰富的属。MIH患者中读取计数最高的细菌包括[细菌名称1]、[细菌名称2]、[细菌名称3]、[细菌名称4]和[细菌名称5]。我们的结果揭示了健康儿童和受MIH影响儿童之间的显著差异,受MIH影响的患者中致病物种([致病细菌名称1]、[致病细菌名称2]和[致病细菌名称3])的优势度和数量更高,多样性降低。这种独特的微生物特征不仅为受MIH影响的患者提供了线索,也为未来的研究铺平了道路,激发了更深入的理解和更大规模的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ff5/11642311/01649f172340/ijms-25-13143-g001.jpg

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