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Characterization of Bacterial Communities in Selected Smokeless Tobacco Products Using 16S rDNA Analysis
The bacterial communities present in smokeless tobacco (ST) products have not previously reported. In this study, we used Next Generation Sequencing to study the bacteria present in U.S.-made dry snuff, moist snuff and Sudanese toombak. Sample diversity and taxonomic abundances were investigated in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718623/ https://www.ncbi.nlm.nih.gov/pubmed/26784944 http://dx.doi.org/10.1371/journal.pone.0146939 |
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author | Tyx, Robert E. Stanfill, Stephen B. Keong, Lisa M. Rivera, Angel J. Satten, Glen A. Watson, Clifford H. |
author_facet | Tyx, Robert E. Stanfill, Stephen B. Keong, Lisa M. Rivera, Angel J. Satten, Glen A. Watson, Clifford H. |
author_sort | Tyx, Robert E. |
collection | PubMed |
description | The bacterial communities present in smokeless tobacco (ST) products have not previously reported. In this study, we used Next Generation Sequencing to study the bacteria present in U.S.-made dry snuff, moist snuff and Sudanese toombak. Sample diversity and taxonomic abundances were investigated in these products. A total of 33 bacterial families from four phyla, Actinobacteria, Firmicutes, Proteobacteria and Bacteroidetes, were identified. U.S.-produced dry snuff products contained a diverse distribution of all four phyla. Moist snuff products were dominated by Firmicutes. Toombak samples contained mainly Actinobacteria and Firmicutes (Aerococcaceae, Enterococcaceae, and Staphylococcaceae). The program PICRUSt (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States) was used to impute the prevalence of genes encoding selected bacterial toxins, antibiotic resistance genes and other pro-inflammatory molecules. PICRUSt also predicted the presence of specific nitrate reductase genes, whose products can contribute to the formation of carcinogenic nitrosamines. Characterization of microbial community abundances and their associated genomes gives us an indication of the presence or absence of pathways of interest and can be used as a foundation for further investigation into the unique microbiological and chemical environments of smokeless tobacco products. |
format | Online Article Text |
id | pubmed-4718623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47186232016-01-30 Characterization of Bacterial Communities in Selected Smokeless Tobacco Products Using 16S rDNA Analysis Tyx, Robert E. Stanfill, Stephen B. Keong, Lisa M. Rivera, Angel J. Satten, Glen A. Watson, Clifford H. PLoS One Research Article The bacterial communities present in smokeless tobacco (ST) products have not previously reported. In this study, we used Next Generation Sequencing to study the bacteria present in U.S.-made dry snuff, moist snuff and Sudanese toombak. Sample diversity and taxonomic abundances were investigated in these products. A total of 33 bacterial families from four phyla, Actinobacteria, Firmicutes, Proteobacteria and Bacteroidetes, were identified. U.S.-produced dry snuff products contained a diverse distribution of all four phyla. Moist snuff products were dominated by Firmicutes. Toombak samples contained mainly Actinobacteria and Firmicutes (Aerococcaceae, Enterococcaceae, and Staphylococcaceae). The program PICRUSt (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States) was used to impute the prevalence of genes encoding selected bacterial toxins, antibiotic resistance genes and other pro-inflammatory molecules. PICRUSt also predicted the presence of specific nitrate reductase genes, whose products can contribute to the formation of carcinogenic nitrosamines. Characterization of microbial community abundances and their associated genomes gives us an indication of the presence or absence of pathways of interest and can be used as a foundation for further investigation into the unique microbiological and chemical environments of smokeless tobacco products. Public Library of Science 2016-01-19 /pmc/articles/PMC4718623/ /pubmed/26784944 http://dx.doi.org/10.1371/journal.pone.0146939 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Tyx, Robert E. Stanfill, Stephen B. Keong, Lisa M. Rivera, Angel J. Satten, Glen A. Watson, Clifford H. Characterization of Bacterial Communities in Selected Smokeless Tobacco Products Using 16S rDNA Analysis |
title | Characterization of Bacterial Communities in Selected Smokeless Tobacco Products Using 16S rDNA Analysis |
title_full | Characterization of Bacterial Communities in Selected Smokeless Tobacco Products Using 16S rDNA Analysis |
title_fullStr | Characterization of Bacterial Communities in Selected Smokeless Tobacco Products Using 16S rDNA Analysis |
title_full_unstemmed | Characterization of Bacterial Communities in Selected Smokeless Tobacco Products Using 16S rDNA Analysis |
title_short | Characterization of Bacterial Communities in Selected Smokeless Tobacco Products Using 16S rDNA Analysis |
title_sort | characterization of bacterial communities in selected smokeless tobacco products using 16s rdna analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718623/ https://www.ncbi.nlm.nih.gov/pubmed/26784944 http://dx.doi.org/10.1371/journal.pone.0146939 |
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