Espinoza Josh L, Torralba Manolito, Leong Pamela, Saffery Richard, Bockmann Michelle, Kuelbs Claire, Singh Suren, Hughes Toby, Craig Jeffrey M, Nelson Karen E, Dupont Chris L
Department of Environment and Sustainability, J. Craig Venter Institute, La Jolla, CA 92037, USA.
Department of Human Biology and Genomic Medicine, J. Craig Venter Institute, La Jolla, CA 92037, USA.
PNAS Nexus. 2022 Oct 18;1(5):pgac239. doi: 10.1093/pnasnexus/pgac239. eCollection 2022 Nov.
Dental caries is a microbial disease and the most common chronic health condition, affecting nearly 3.5 billion people worldwide. In this study, we used a multiomics approach to characterize the supragingival plaque microbiome of 91 Australian children, generating 658 bacterial and 189 viral metagenome-assembled genomes with transcriptional profiling and gene-expression network analysis. We developed a reproducible pipeline for clustering sample-specific genomes to integrate metagenomics and metatranscriptomics analyses regardless of biosample overlap. We introduce novel feature engineering and compositionally-aware ensemble network frameworks while demonstrating their utility for investigating regime shifts associated with caries dysbiosis. These methods can be applied when differential abundance modeling does not capture statistical enrichments or the results from such analysis are not adequate for providing deeper insight into disease. We identified which organisms and metabolic pathways were central in a coexpression network as well as how these networks were rewired between caries and caries-free phenotypes. Our findings provide evidence of a core bacterial microbiome that was transcriptionally active in the supragingival plaque of all participants regardless of phenotype, but also show highly diagnostic changes in the ways that organisms interact. Specifically, many organisms exhibit high connectedness with central carbon metabolism to and this shift serves a bridge between phenotypes. Our evidence supports the hypothesis that caries is a multifactorial ecological disease.
龋齿是一种微生物疾病,也是最常见的慢性健康问题,全球近35亿人受其影响。在本研究中,我们采用多组学方法对91名澳大利亚儿童的龈上菌斑微生物群进行表征,通过转录谱分析和基因表达网络分析生成了658个细菌和189个病毒宏基因组组装基因组。我们开发了一种可重复的流程,用于对样本特异性基因组进行聚类,以整合宏基因组学和宏转录组学分析,而不考虑生物样本的重叠情况。我们引入了新颖的特征工程和成分感知集成网络框架,同时展示了它们在研究与龋齿生态失调相关的状态转变方面的效用。当差异丰度建模无法捕捉统计富集情况或此类分析结果不足以深入洞察疾病时,这些方法可以应用。我们确定了哪些生物体和代谢途径在共表达网络中处于核心地位,以及这些网络在龋齿和无龋表型之间是如何重新连接的。我们的研究结果提供了证据,表明存在一个核心细菌微生物群,在所有参与者的龈上菌斑中均具有转录活性,而不论其表型如何,但也显示出生物体相互作用方式的高度诊断性变化。具体而言,许多生物体与中心碳代谢具有高度关联性,这种转变在不同表型之间起到了桥梁作用。我们的证据支持龋齿是一种多因素生态疾病这一假说。