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Subgingival Microbiome Colonization and Cytokine Production during Early Dental Implant Healing

Little is known about longitudinal development of the peri-implant subgingival microbiome and cytokine production as a new sulcus forms after dental implant placement. Therefore, the purpose of this observational study was to evaluate simultaneous longitudinal changes in the oral microbiome and cyto...

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Autores principales: Payne, Jeffrey B., Johnson, Paul G., Kok, Car Reen, Gomes-Neto, João C., Ramer-Tait, Amanda E., Schmid, Marian J., Hutkins, Robert W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705808/
https://www.ncbi.nlm.nih.gov/pubmed/29202047
http://dx.doi.org/10.1128/mSphereDirect.00527-17
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author Payne, Jeffrey B.
Johnson, Paul G.
Kok, Car Reen
Gomes-Neto, João C.
Ramer-Tait, Amanda E.
Schmid, Marian J.
Hutkins, Robert W.
author_facet Payne, Jeffrey B.
Johnson, Paul G.
Kok, Car Reen
Gomes-Neto, João C.
Ramer-Tait, Amanda E.
Schmid, Marian J.
Hutkins, Robert W.
author_sort Payne, Jeffrey B.
collection PubMed
description Little is known about longitudinal development of the peri-implant subgingival microbiome and cytokine production as a new sulcus forms after dental implant placement. Therefore, the purpose of this observational study was to evaluate simultaneous longitudinal changes in the oral microbiome and cytokine production in the developing peri-implant sulcus compared to control natural teeth. Four and 12 weeks after implant placement and abutment connection, a dental implant and a natural tooth were sampled in 25 patients for subgingival plaque and gingival crevicular fluid (GCF [around teeth] and peri-implant crevicular fluid [PICF] around implants). DNA from plaque samples was extracted and sequenced using Illumina-based 16S rRNA sequencing. GCF and PICF samples were analyzed using a customized Milliplex human cytokine and chemokine magnetic bead panel. Beta diversity analysis revealed that natural teeth and implants had similar subgingival microbiomes, while teeth had greater alpha diversity than implants. At the genus level, however, few differences were noted between teeth and dental implants over 12 weeks. Specifically, Actinomyces and Selenomonas were significantly elevated around teeth versus dental implants at both 4 weeks and 12 weeks, while Corynebacterium and Campylobacter were significantly elevated only at 4 weeks around teeth. The only difference between PICF and GCF biomarkers was significantly elevated granulocyte-macrophage colony-stimulating factor levels around teeth versus dental implants at the 4-week visit. The subgingival microbiome and cytokine production were similar between teeth and implants during early healing, suggesting that these profiles are driven by the patient following dental implant placement and are not determined by anatomical niche. IMPORTANCE Dental implants are a common treatment option offered to patients for tooth replacement. However, little is known regarding initial colonization of the subgingival microbiome and simultaneous longitudinal cytokine production in humans during the early healing phase following implant placement. We report findings from an in vivo study that assessed initial colonization of the subgingival microbiome and concomitant early cytokine production in a newly formed anatomical space, namely, an implant sulcus. This approach may be useful in future interventional studies to influence dental implant success. Our data showed that the subgingival microbiome and cytokine profile were similar for control natural teeth and dental implants at both 4 and 12 weeks after implant placement. These data suggest that these profiles are driven by the patient and not by anatomical location (i.e., tooth versus dental implant).
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spelling pubmed-57058082017-12-01 Subgingival Microbiome Colonization and Cytokine Production during Early Dental Implant Healing Payne, Jeffrey B. Johnson, Paul G. Kok, Car Reen Gomes-Neto, João C. Ramer-Tait, Amanda E. Schmid, Marian J. Hutkins, Robert W. mSphere Research Article Little is known about longitudinal development of the peri-implant subgingival microbiome and cytokine production as a new sulcus forms after dental implant placement. Therefore, the purpose of this observational study was to evaluate simultaneous longitudinal changes in the oral microbiome and cytokine production in the developing peri-implant sulcus compared to control natural teeth. Four and 12 weeks after implant placement and abutment connection, a dental implant and a natural tooth were sampled in 25 patients for subgingival plaque and gingival crevicular fluid (GCF [around teeth] and peri-implant crevicular fluid [PICF] around implants). DNA from plaque samples was extracted and sequenced using Illumina-based 16S rRNA sequencing. GCF and PICF samples were analyzed using a customized Milliplex human cytokine and chemokine magnetic bead panel. Beta diversity analysis revealed that natural teeth and implants had similar subgingival microbiomes, while teeth had greater alpha diversity than implants. At the genus level, however, few differences were noted between teeth and dental implants over 12 weeks. Specifically, Actinomyces and Selenomonas were significantly elevated around teeth versus dental implants at both 4 weeks and 12 weeks, while Corynebacterium and Campylobacter were significantly elevated only at 4 weeks around teeth. The only difference between PICF and GCF biomarkers was significantly elevated granulocyte-macrophage colony-stimulating factor levels around teeth versus dental implants at the 4-week visit. The subgingival microbiome and cytokine production were similar between teeth and implants during early healing, suggesting that these profiles are driven by the patient following dental implant placement and are not determined by anatomical niche. IMPORTANCE Dental implants are a common treatment option offered to patients for tooth replacement. However, little is known regarding initial colonization of the subgingival microbiome and simultaneous longitudinal cytokine production in humans during the early healing phase following implant placement. We report findings from an in vivo study that assessed initial colonization of the subgingival microbiome and concomitant early cytokine production in a newly formed anatomical space, namely, an implant sulcus. This approach may be useful in future interventional studies to influence dental implant success. Our data showed that the subgingival microbiome and cytokine profile were similar for control natural teeth and dental implants at both 4 and 12 weeks after implant placement. These data suggest that these profiles are driven by the patient and not by anatomical location (i.e., tooth versus dental implant). American Society for Microbiology 2017-11-29 /pmc/articles/PMC5705808/ /pubmed/29202047 http://dx.doi.org/10.1128/mSphereDirect.00527-17 Text en Copyright © 2017 Payne et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Payne, Jeffrey B.
Johnson, Paul G.
Kok, Car Reen
Gomes-Neto, João C.
Ramer-Tait, Amanda E.
Schmid, Marian J.
Hutkins, Robert W.
Subgingival Microbiome Colonization and Cytokine Production during Early Dental Implant Healing
title Subgingival Microbiome Colonization and Cytokine Production during Early Dental Implant Healing
title_full Subgingival Microbiome Colonization and Cytokine Production during Early Dental Implant Healing
title_fullStr Subgingival Microbiome Colonization and Cytokine Production during Early Dental Implant Healing
title_full_unstemmed Subgingival Microbiome Colonization and Cytokine Production during Early Dental Implant Healing
title_short Subgingival Microbiome Colonization and Cytokine Production during Early Dental Implant Healing
title_sort subgingival microbiome colonization and cytokine production during early dental implant healing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705808/
https://www.ncbi.nlm.nih.gov/pubmed/29202047
http://dx.doi.org/10.1128/mSphereDirect.00527-17
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