Differential network analysis of oral microbiome metatranscriptomes identifies community scale metabolic restructuring in dental caries

Author:

Espinoza Josh L123ORCID,Torralba Manolito3,Leong Pamela4,Saffery Richard4ORCID,Bockmann Michelle5,Kuelbs Claire2,Singh Suren3,Hughes Toby5,Craig Jeffrey M46,Nelson Karen E23,Dupont Chris L12

Affiliation:

1. Department of Environment and Sustainability, J. Craig Venter Institute , La Jolla, CA 92037 , USA

2. Department of Human Biology and Genomic Medicine, J. Craig Venter Institute , La Jolla, CA 92037 , USA

3. Department of Human Biology and Genomic Medicine, J. Craig Venter Institute , Rockville, MD 20850 , USA

4. Epigenetics, Murdoch Children's Research Institute and Department of Paediatrics, The University of Melbourne , Parkville, VIC 3052 , Australia

5. Adelaide Dental School, The University of Adelaide , Adelaide, SA 5005 , Australia

6. IMPACT Strategic Research Centre, Deakin University School of Medicine , Geelong, VIC 3220 , Australia

Abstract

Abstract 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 Cardiobacterium and this shift serves a bridge between phenotypes. Our evidence supports the hypothesis that caries is a multifactorial ecological disease.

Funder

National Institutes of Health

National Health and Medical Research Council

Publisher

Oxford University Press (OUP)

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