Multistability and hysteresis in states of oral microbiota: Is it impacting the dental clinical cohort studies?

Author:

Mangal Utkarsh12ORCID,Noh Kowoon234,Lee Seeyoon1,Cha Jae‐Kook5,Song Je Seon67ORCID,Cha Jung‐Yul12,Lee Kee‐Joon12,Kim Kwang‐Mahn3,Kwon Jae‐Sung34ORCID,Choi Sung‐Hwan12ORCID

Affiliation:

1. Department of Orthodontics Yonsei University College of Dentistry Seoul Korea

2. Institute of Craniofacial Deformity Yonsei University College of Dentistry Seoul Korea

3. Department and Research Institute of Dental Biomaterials and Bioengineering Yonsei University College of Dentistry Seoul Korea

4. BK21 FOUR Project Yonsei University College of Dentistry Seoul Korea

5. Department of Periodontology, Research Institute of Periodontal Regeneration Yonsei University College of Dentistry Seoul Korea

6. Department of Pediatric Dentistry Yonsei University College of Dentistry Seoul Korea

7. Oral Science Research Center, College of Dentistry Yonsei University Seoul Korea

Abstract

AbstractIntroductionMicrobiome from a “healthy cohort” is used as a reference for comparison to cases and intervention. However, the studies with cohort‐based clinical research have not sufficiently accounted for the multistability in oral microbial community. The screening is limited to phenotypic features with marked variations in microbial genomic markers. Herein, we aimed to assess the stability of the oral microbiome across time from an intervention‐free “healthy” cohort.MethodsWe obtained 33 supragingival samples of 11 healthy participants from the biobank. For each participant, we processed one sample as baseline (T0) and two samples spaced at 1‐month (T1) and 3‐month (T2) intervals for 16S ribosomal RNA gene sequencing analysis.ResultsWe observed that taxonomic profiling had a similar pattern of dominant genera, namely, Rothia, Prevotella, and Hemophilus, at all time points. Shannon diversity revealed a significant increase from T0 (p < .05). Bray Curtis dissimilarity was significant (R = −.02, p < .01) within the cohort at each time point. Community stability had negative correlation to synchrony (r = −.739; p = .009) and variance (r = −.605; p = .048) of the species. Clustering revealed marked differences in the grouping patterns between the three time points. For all time points, the clusters presented a substantially dissimilar set of differentially abundant taxonomic and functional biomarkers.ConclusionOur observations indicate towards the presence of multistable states within the oral microbiome in an intervention‐free healthy cohort. For a conclusive and meaningful long‐term reference, dental clinical research should account for multistability in the personalized therapy approach to improve the identification and classification of reliable markers.

Funder

Yonsei University College of Dentistry

Publisher

Wiley

Subject

Periodontics

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