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深度宏基因组学研究了龋齿过程中的口腔微生物组,揭示了新的分类群和与宿主分子的共同出现。

Deep metagenomics examines the oral microbiome during dental caries, revealing novel taxa and co-occurrences with host molecules.

机构信息

Genomic Medicine Group, J. Craig Venter Institute, La Jolla, California 92037, USA.

Systems Biology Group, Flatiron Institute, New York, New York 10010, USA.

出版信息

Genome Res. 2021 Jan;31(1):64-74. doi: 10.1101/gr.265645.120. Epub 2020 Nov 25.

Abstract

Dental caries, the most common chronic infectious disease worldwide, has a complex etiology involving the interplay of microbial and host factors that are not completely understood. In this study, the oral microbiome and 38 host cytokines and chemokines were analyzed across 23 children with caries and 24 children with healthy dentition. De novo assembly of metagenomic sequencing obtained 527 metagenome-assembled genomes (MAGs), representing 150 bacterial species. Forty-two of these species had no genomes in public repositories, thereby representing novel taxa. These new genomes greatly expanded the known pangenomes of many oral clades, including the enigmatic Saccharibacteria clades G3 and G6, which had distinct functional repertoires compared to other oral Saccharibacteria. Saccharibacteria are understood to be obligate epibionts, which are dependent on host bacteria. These data suggest that the various Saccharibacteria clades may rely on their hosts for highly distinct metabolic requirements, which would have significant evolutionary and ecological implications. Across the study group, , , and spp. were associated with good dental health, whereas spp., , and (Epstein-Barr virus [EBV]) were more prevalent in children with caries. Finally, 10 of the host immunological markers were significantly elevated in the caries group, and co-occurrence analysis provided an atlas of potential relationships between microbes and host immunological molecules. Overall, this study illustrated the oral microbiome at an unprecedented resolution and contributed several leads for further study that will increase the understanding of caries pathogenesis and guide therapeutic development.

摘要

龋齿是全球最常见的慢性传染病,其病因复杂,涉及微生物和宿主因素的相互作用,但这些因素尚未完全被理解。在这项研究中,分析了 23 名龋齿儿童和 24 名健康牙齿儿童的口腔微生物组和 38 种宿主细胞因子和趋化因子。宏基因组测序的从头组装获得了 527 个宏基因组组装基因组(MAG),代表 150 种细菌物种。其中 42 种细菌在公共数据库中没有基因组,因此代表了新的分类单元。这些新的基因组极大地扩展了许多口腔类群的已知泛基因组,包括神秘的 Saccharibacteria 类群 G3 和 G6,它们与其他口腔 Saccharibacteria 相比具有独特的功能谱。Saccharibacteria 被认为是专性的表生菌,它们依赖于宿主细菌。这些数据表明,各种 Saccharibacteria 类群可能依赖其宿主满足高度独特的代谢需求,这将具有重大的进化和生态意义。在整个研究组中, , , 和 spp. 与良好的牙齿健康相关,而 spp., , 和 (EBV)在龋齿儿童中更为普遍。最后,龋齿组中 10 种宿主免疫标志物显著升高,共现分析提供了微生物和宿主免疫分子之间潜在关系的图谱。总的来说,这项研究以空前的分辨率描绘了口腔微生物组,并为进一步研究提供了一些线索,这将增加对龋齿发病机制的理解并指导治疗方法的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5381/7849383/f62860bc6076/64f01.jpg

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