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Oral Microbiota Profile Associates with Sugar Intake and Taste Preference Genes

Oral microbiota ecology is influenced by environmental and host conditions, but few studies have evaluated associations between untargeted measures of the entire oral microbiome and potentially relevant environmental and host factors. This study aimed to identify salivary microbiota cluster groups u...

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Autores principales: Esberg, Anders, Haworth, Simon, Hasslöf, Pamela, Lif Holgerson, Pernilla, Johansson, Ingegerd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7146170/
https://www.ncbi.nlm.nih.gov/pubmed/32138214
http://dx.doi.org/10.3390/nu12030681
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author Esberg, Anders
Haworth, Simon
Hasslöf, Pamela
Lif Holgerson, Pernilla
Johansson, Ingegerd
author_facet Esberg, Anders
Haworth, Simon
Hasslöf, Pamela
Lif Holgerson, Pernilla
Johansson, Ingegerd
author_sort Esberg, Anders
collection PubMed
description Oral microbiota ecology is influenced by environmental and host conditions, but few studies have evaluated associations between untargeted measures of the entire oral microbiome and potentially relevant environmental and host factors. This study aimed to identify salivary microbiota cluster groups using hierarchical cluster analyses (Wards method) based on 16S rRNA gene amplicon sequencing, and identify lifestyle and host factors which were associated with these groups. Group members (n = 175) were distinctly separated by microbiota profiles and differed in reported sucrose intake and allelic variation in the taste-preference-associated genes TAS1R1 (rs731024) and GNAT3 (rs2074673). Groups with higher sucrose intake were either characterized by a wide panel of species or phylotypes with fewer aciduric species, or by a narrower profile that included documented aciduric- and caries-associated species. The inferred functional profiles of the latter type were dominated by metabolic pathways associated with the carbohydrate metabolism with enrichment of glycosidase functions. In conclusion, this study supported in vivo associations between sugar intake and oral microbiota ecology, but it also found evidence for a variable microbiota response to sugar, highlighting the importance of modifying host factors and microbes beyond the commonly targeted acidogenic and acid-tolerant species. The results should be confirmed under controlled settings with comprehensive phenotypic and genotypic data.
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spelling pubmed-71461702020-04-15 Oral Microbiota Profile Associates with Sugar Intake and Taste Preference Genes Esberg, Anders Haworth, Simon Hasslöf, Pamela Lif Holgerson, Pernilla Johansson, Ingegerd Nutrients Article Oral microbiota ecology is influenced by environmental and host conditions, but few studies have evaluated associations between untargeted measures of the entire oral microbiome and potentially relevant environmental and host factors. This study aimed to identify salivary microbiota cluster groups using hierarchical cluster analyses (Wards method) based on 16S rRNA gene amplicon sequencing, and identify lifestyle and host factors which were associated with these groups. Group members (n = 175) were distinctly separated by microbiota profiles and differed in reported sucrose intake and allelic variation in the taste-preference-associated genes TAS1R1 (rs731024) and GNAT3 (rs2074673). Groups with higher sucrose intake were either characterized by a wide panel of species or phylotypes with fewer aciduric species, or by a narrower profile that included documented aciduric- and caries-associated species. The inferred functional profiles of the latter type were dominated by metabolic pathways associated with the carbohydrate metabolism with enrichment of glycosidase functions. In conclusion, this study supported in vivo associations between sugar intake and oral microbiota ecology, but it also found evidence for a variable microbiota response to sugar, highlighting the importance of modifying host factors and microbes beyond the commonly targeted acidogenic and acid-tolerant species. The results should be confirmed under controlled settings with comprehensive phenotypic and genotypic data. MDPI 2020-03-03 /pmc/articles/PMC7146170/ /pubmed/32138214 http://dx.doi.org/10.3390/nu12030681 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Esberg, Anders
Haworth, Simon
Hasslöf, Pamela
Lif Holgerson, Pernilla
Johansson, Ingegerd
Oral Microbiota Profile Associates with Sugar Intake and Taste Preference Genes
title Oral Microbiota Profile Associates with Sugar Intake and Taste Preference Genes
title_full Oral Microbiota Profile Associates with Sugar Intake and Taste Preference Genes
title_fullStr Oral Microbiota Profile Associates with Sugar Intake and Taste Preference Genes
title_full_unstemmed Oral Microbiota Profile Associates with Sugar Intake and Taste Preference Genes
title_short Oral Microbiota Profile Associates with Sugar Intake and Taste Preference Genes
title_sort oral microbiota profile associates with sugar intake and taste preference genes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7146170/
https://www.ncbi.nlm.nih.gov/pubmed/32138214
http://dx.doi.org/10.3390/nu12030681
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