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Comparison of the oral microbiome in mouthwash and whole saliva samples

Population-based epidemiologic studies can provide important insight regarding the role of the microbiome in human health and disease. Buccal cells samples using commercial mouthwash have been obtained in large prospective cohorts for the purpose of studying human genomic DNA. We aimed to better und...

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Autores principales: Fan, Xiaozhou, Peters, Brandilyn A., Min, Deborah, Ahn, Jiyoung, Hayes, Richard B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5894969/
https://www.ncbi.nlm.nih.gov/pubmed/29641531
http://dx.doi.org/10.1371/journal.pone.0194729
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author Fan, Xiaozhou
Peters, Brandilyn A.
Min, Deborah
Ahn, Jiyoung
Hayes, Richard B.
author_facet Fan, Xiaozhou
Peters, Brandilyn A.
Min, Deborah
Ahn, Jiyoung
Hayes, Richard B.
author_sort Fan, Xiaozhou
collection PubMed
description Population-based epidemiologic studies can provide important insight regarding the role of the microbiome in human health and disease. Buccal cells samples using commercial mouthwash have been obtained in large prospective cohorts for the purpose of studying human genomic DNA. We aimed to better understand if these mouthwash samples are also a valid resource for the study of the oral microbiome. We collected one saliva sample and one Scope mouthwash sample from 10 healthy subjects. Bacterial 16S rRNA genes from both types of samples were amplified, sequenced, and assigned to bacterial taxa. We comprehensively compared these paired samples for bacterial community composition and individual taxonomic abundance. We found that mouthwash samples yielded similar amount of bacterial DNA as saliva samples (p from Student’s t-test for paired samples = 0.92). Additionally, the paired samples had similar within sample diversity (p from = 0.33 for richness, and p = 0.51 for Shannon index), and clustered as pairs for diversity when analyzed by unsupervised hierarchical cluster analysis. No significant difference was found in the paired samples with respect to the taxonomic abundance of major bacterial phyla, Bacteroidetes, Firmicutes, Proteobacteria, Fusobacteria, and Actinobacteria (FDR adjusted q values from Wilcoxin signed-rank test = 0.15, 0.15, 0.87, 1.00 and 0.15, respectively), and all identified genera, including genus Streptococcus (q = 0.21), Prevotella (q = 0.25), Neisseria (q = 0.37), Veillonella (q = 0.73), Fusobacterium (q = 0.19), and Porphyromonas (q = 0.60). These results show that mouthwash samples perform similarly to saliva samples for analysis of the oral microbiome. Mouthwash samples collected originally for analysis of human DNA are also a resource suitable for human microbiome research.
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spelling pubmed-58949692018-05-04 Comparison of the oral microbiome in mouthwash and whole saliva samples Fan, Xiaozhou Peters, Brandilyn A. Min, Deborah Ahn, Jiyoung Hayes, Richard B. PLoS One Research Article Population-based epidemiologic studies can provide important insight regarding the role of the microbiome in human health and disease. Buccal cells samples using commercial mouthwash have been obtained in large prospective cohorts for the purpose of studying human genomic DNA. We aimed to better understand if these mouthwash samples are also a valid resource for the study of the oral microbiome. We collected one saliva sample and one Scope mouthwash sample from 10 healthy subjects. Bacterial 16S rRNA genes from both types of samples were amplified, sequenced, and assigned to bacterial taxa. We comprehensively compared these paired samples for bacterial community composition and individual taxonomic abundance. We found that mouthwash samples yielded similar amount of bacterial DNA as saliva samples (p from Student’s t-test for paired samples = 0.92). Additionally, the paired samples had similar within sample diversity (p from = 0.33 for richness, and p = 0.51 for Shannon index), and clustered as pairs for diversity when analyzed by unsupervised hierarchical cluster analysis. No significant difference was found in the paired samples with respect to the taxonomic abundance of major bacterial phyla, Bacteroidetes, Firmicutes, Proteobacteria, Fusobacteria, and Actinobacteria (FDR adjusted q values from Wilcoxin signed-rank test = 0.15, 0.15, 0.87, 1.00 and 0.15, respectively), and all identified genera, including genus Streptococcus (q = 0.21), Prevotella (q = 0.25), Neisseria (q = 0.37), Veillonella (q = 0.73), Fusobacterium (q = 0.19), and Porphyromonas (q = 0.60). These results show that mouthwash samples perform similarly to saliva samples for analysis of the oral microbiome. Mouthwash samples collected originally for analysis of human DNA are also a resource suitable for human microbiome research. Public Library of Science 2018-04-11 /pmc/articles/PMC5894969/ /pubmed/29641531 http://dx.doi.org/10.1371/journal.pone.0194729 Text en © 2018 Fan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Fan, Xiaozhou
Peters, Brandilyn A.
Min, Deborah
Ahn, Jiyoung
Hayes, Richard B.
Comparison of the oral microbiome in mouthwash and whole saliva samples
title Comparison of the oral microbiome in mouthwash and whole saliva samples
title_full Comparison of the oral microbiome in mouthwash and whole saliva samples
title_fullStr Comparison of the oral microbiome in mouthwash and whole saliva samples
title_full_unstemmed Comparison of the oral microbiome in mouthwash and whole saliva samples
title_short Comparison of the oral microbiome in mouthwash and whole saliva samples
title_sort comparison of the oral microbiome in mouthwash and whole saliva samples
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5894969/
https://www.ncbi.nlm.nih.gov/pubmed/29641531
http://dx.doi.org/10.1371/journal.pone.0194729
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