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Bacteria in the cavity-restoration interface after varying periods of clinical service — SEM description of distribution and 16S rRNA gene sequence identification of isolates

OBJECTIVES: To use extracted human teeth with amalgam (n = 26) or GIC (n = 3) restorations in service up to 20 years to evaluate microbiota at the cavity/restoration interface by SEM or culture. MATERIALS AND METHODS: Extracted teeth with intracoronal restorations (n = 20) of known history (2–20 yea...

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Autores principales: Arora, Roopinder Kaur, Mordan, Nicola J., Spratt, David A., Ng, Yuan Ling, Gulabivala, Kishor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276561/
https://www.ncbi.nlm.nih.gov/pubmed/35359188
http://dx.doi.org/10.1007/s00784-022-04473-2
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author Arora, Roopinder Kaur
Mordan, Nicola J.
Spratt, David A.
Ng, Yuan Ling
Gulabivala, Kishor
author_facet Arora, Roopinder Kaur
Mordan, Nicola J.
Spratt, David A.
Ng, Yuan Ling
Gulabivala, Kishor
author_sort Arora, Roopinder Kaur
collection PubMed
description OBJECTIVES: To use extracted human teeth with amalgam (n = 26) or GIC (n = 3) restorations in service up to 20 years to evaluate microbiota at the cavity/restoration interface by SEM or culture. MATERIALS AND METHODS: Extracted teeth with intracoronal restorations (n = 20) of known history (2–20 years) were fixed, split, and prepared for SEM to ascertain the pattern and structure of bacterial aggregates on cavity and restoration surfaces. Another 9 teeth were anaerobically decontaminated, split and sampled (cavity/restorations), and cultured (anaerobically, aerobically); recovered isolates were identified by 16S rRNA gene sequencing. RESULTS: SEM showed rods, cocci, and filaments in 11/20 teeth (55%) on cavity and corresponding restoration surfaces; 4/20 (20%) on neither surface; 1/20 (5%) on just cavity; and 4/20 (20%) on just restoration. Microbial growth extended from marginal openings into the deeper interfacial microspace to varying extents but was not always evident. Restoration size or age did not predict bacterial presence. Bacteria-free surfaces (cavity/amalgam) showed possible calcification. Cultivation yielded 160 isolates, mainly Gram-positive (86%) and facultative (81%); and morphotypes of rods (43%), cocci (36%), and cocco-bacilli (18%) belonging to Actinobacteria (45%) and Firmicutes (50%). The most frequent genera were Staphylococcus, Streptococcus, Actinomyces, and Lactobacillus. Biofilms on cavity and restoration appeared independent of each other. CONCLUSIONS: Cavity and amalgam surfaces were independently colonised and some not. The penetration of microbiota into marginal gaps varied; resembled root caries and was dominated by Gram-positive species. CLINICAL RELEVANCE: Marginal gaps around restorations are unavoidable but are not always colonised by bacteria after long-term clinical service. Calcification of biofilms in the restorative interface may prevent further colonisation. The viable microbiota in the restorative interface resembled root caries and may be subject to ecological fluxes of activity and arrest and therefore preventative management.
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spelling pubmed-92765612022-07-14 Bacteria in the cavity-restoration interface after varying periods of clinical service — SEM description of distribution and 16S rRNA gene sequence identification of isolates Arora, Roopinder Kaur Mordan, Nicola J. Spratt, David A. Ng, Yuan Ling Gulabivala, Kishor Clin Oral Investig Original Article OBJECTIVES: To use extracted human teeth with amalgam (n = 26) or GIC (n = 3) restorations in service up to 20 years to evaluate microbiota at the cavity/restoration interface by SEM or culture. MATERIALS AND METHODS: Extracted teeth with intracoronal restorations (n = 20) of known history (2–20 years) were fixed, split, and prepared for SEM to ascertain the pattern and structure of bacterial aggregates on cavity and restoration surfaces. Another 9 teeth were anaerobically decontaminated, split and sampled (cavity/restorations), and cultured (anaerobically, aerobically); recovered isolates were identified by 16S rRNA gene sequencing. RESULTS: SEM showed rods, cocci, and filaments in 11/20 teeth (55%) on cavity and corresponding restoration surfaces; 4/20 (20%) on neither surface; 1/20 (5%) on just cavity; and 4/20 (20%) on just restoration. Microbial growth extended from marginal openings into the deeper interfacial microspace to varying extents but was not always evident. Restoration size or age did not predict bacterial presence. Bacteria-free surfaces (cavity/amalgam) showed possible calcification. Cultivation yielded 160 isolates, mainly Gram-positive (86%) and facultative (81%); and morphotypes of rods (43%), cocci (36%), and cocco-bacilli (18%) belonging to Actinobacteria (45%) and Firmicutes (50%). The most frequent genera were Staphylococcus, Streptococcus, Actinomyces, and Lactobacillus. Biofilms on cavity and restoration appeared independent of each other. CONCLUSIONS: Cavity and amalgam surfaces were independently colonised and some not. The penetration of microbiota into marginal gaps varied; resembled root caries and was dominated by Gram-positive species. CLINICAL RELEVANCE: Marginal gaps around restorations are unavoidable but are not always colonised by bacteria after long-term clinical service. Calcification of biofilms in the restorative interface may prevent further colonisation. The viable microbiota in the restorative interface resembled root caries and may be subject to ecological fluxes of activity and arrest and therefore preventative management. Springer Berlin Heidelberg 2022-04-01 2022 /pmc/articles/PMC9276561/ /pubmed/35359188 http://dx.doi.org/10.1007/s00784-022-04473-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Arora, Roopinder Kaur
Mordan, Nicola J.
Spratt, David A.
Ng, Yuan Ling
Gulabivala, Kishor
Bacteria in the cavity-restoration interface after varying periods of clinical service — SEM description of distribution and 16S rRNA gene sequence identification of isolates
title Bacteria in the cavity-restoration interface after varying periods of clinical service — SEM description of distribution and 16S rRNA gene sequence identification of isolates
title_full Bacteria in the cavity-restoration interface after varying periods of clinical service — SEM description of distribution and 16S rRNA gene sequence identification of isolates
title_fullStr Bacteria in the cavity-restoration interface after varying periods of clinical service — SEM description of distribution and 16S rRNA gene sequence identification of isolates
title_full_unstemmed Bacteria in the cavity-restoration interface after varying periods of clinical service — SEM description of distribution and 16S rRNA gene sequence identification of isolates
title_short Bacteria in the cavity-restoration interface after varying periods of clinical service — SEM description of distribution and 16S rRNA gene sequence identification of isolates
title_sort bacteria in the cavity-restoration interface after varying periods of clinical service — sem description of distribution and 16s rrna gene sequence identification of isolates
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276561/
https://www.ncbi.nlm.nih.gov/pubmed/35359188
http://dx.doi.org/10.1007/s00784-022-04473-2
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