Differential oral microbiome in nonhuman primates from periodontitis-susceptible and periodontitis-resistant matrilines

Jeffrey L. Ebersole, Sreenatha Kirakodu, Octovio Gonzalez

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1 Scopus citations

Abstract

Rhesus monkeys (n = 36) exhibiting a healthy periodontium at baseline were used to induce progressing periodontitis through ligature placement around premolar/molar teeth. Bacterial samples were collected at baseline, 0.5, 1, and 3 months of disease and at 5 months for disease resolution. The animals were distributed into two groups (18/group): 3–7 years (young) and 12–23 years (adult) and stratified based upon matriline susceptibility to periodontitis (PDS, susceptible; PDR, resistant). A total of 444 operational taxonomic units (OTUs) with 100 microbes representing a core microbiome present in ≥75% of the samples were identified. Only 48% of the major phylotypes overlapped in the PDS and PDR samples. Different OTU abundance patterns were seen in young animals from the PDS and PDR matrilines, with qualitative similarities during disease and the relative abundance of phylotypes becoming less diverse. In adults, 23 OTUs were increased during disease in PDS samples and 24 in PDR samples; however, only five were common between these groups. Greater diversity of OTU relative abundance at baseline was observed with adult compared to young oral samples from both the PDS and PDR groups. With disease initiation (2 weeks), less diversity of relative abundance and some distinctive increases in specific OTUs were noted. By 1 month, there was considerable qualitative homogeneity in the major OTUs in both groups; however, by 3 months, there was an exacerbation of both qualitative and quantitative differences in the dominant OTUs between the PDS and PDR samples. These results support that some differences in disease expression related to matriline (familial) periodontitis risk may be explained by microbiome features.

Original languageEnglish
Pages (from-to)93-114
Number of pages22
JournalMolecular Oral Microbiology
Volume38
Issue number2
DOIs
StatePublished - Apr 2023

Bibliographical note

Publisher Copyright:
© 2022 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Funding

This work was supported by National Institute of Health grant P20GM103538. We express our gratitude to the Caribbean Primate Research Center (CPRC) supported by grant P40RR03640 and the Center for Oral Health Research in the College of Dentistry at the University of Kentucky. We thank Drs. M. J. Novak (University of Kentucky) and L. Orraca (University of Puerto Rico) for their support in the clinical aspects of the protocol. We thank Drs. J. Gonzalez Martinez and A.G. Burgos Rodriguez from the Caribbean Primate Research Center for animal husbandry and sampling support. We also thank the Genomic Core Laboratory of University Kentucky for their invaluable technical and data management assistance. This work was supported by National Institute of Health grant P20GM103538. We express our gratitude to the Caribbean Primate Research Center (CPRC) supported by grant P40RR03640 and the Center for Oral Health Research in the College of Dentistry at the University of Kentucky. We thank Drs. M. J. Novak (University of Kentucky) and L. Orraca (University of Puerto Rico) for their support in the clinical aspects of the protocol. We thank Drs. J. Gonzalez Martinez and A.G. Burgos Rodriguez from the Caribbean Primate Research Center for animal husbandry and sampling support. We also thank the Genomic Core Laboratory of University Kentucky for their invaluable technical and data management assistance.

FundersFunder number
Caribbean Primate Research CenterP40RR03640
National Institutes of Health (NIH)P20GM103538
National Institutes of Health (NIH)
University of Kentucky
University of Kentucky College of Dentistry
Universidad de Puerto Rico

    Keywords

    • matrilines
    • microbiome
    • nonhuman primate
    • periodontitis

    ASJC Scopus subject areas

    • Microbiology
    • Immunology
    • General Dentistry
    • Microbiology (medical)

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