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Microbial Diversity and Interaction Specificity in Kombucha Tea Fermentations
Despite the popularity of kombucha tea, the distribution of different microbes across kombucha ferments and how those microbes interact within communities are not well characterized. Using metagenomics, comparative genomics, synthetic community experiments, and metabolomics, we determined the taxono...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238417/ https://www.ncbi.nlm.nih.gov/pubmed/35670539 http://dx.doi.org/10.1128/msystems.00157-22 |
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author | Landis, Elizabeth A. Fogarty, Emily Edwards, John C. Popa, Otilia Eren, A. Murat Wolfe, Benjamin E. |
author_facet | Landis, Elizabeth A. Fogarty, Emily Edwards, John C. Popa, Otilia Eren, A. Murat Wolfe, Benjamin E. |
author_sort | Landis, Elizabeth A. |
collection | PubMed |
description | Despite the popularity of kombucha tea, the distribution of different microbes across kombucha ferments and how those microbes interact within communities are not well characterized. Using metagenomics, comparative genomics, synthetic community experiments, and metabolomics, we determined the taxonomic, ecological, and functional diversity of 23 distinct kombuchas from across the United States. Shotgun metagenomic sequencing demonstrated that the bacterium Komagataeibacter rhaeticus and the yeast Brettanomyces bruxellensis were the most common microbes in the sampled kombucha communities. To determine the specificity of bacterium-yeast interactions, we experimentally quantified microbial interactions within kombucha biofilms by measuring densities of interacting species and biofilm production. In pairwise combinations of bacteria and yeast, B. bruxellensis and individual strains of Komagataeibacter spp. were sufficient to form kombucha fermentations with robust biofilms, but Zygosaccharomyces bisporus, another yeast found in kombucha, did not stimulate bacteria to produce biofilms. Profiling the spent media of both yeast species using nuclear magnetic resonance spectroscopy suggested that the enhanced ability of B. bruxellensis to ferment and produce key metabolites in sucrose-sweetened tea may explain why it stimulates biofilm formation. Comparative genomics demonstrated that Komagataeibacter spp. with >99% genomic similarity can still have dramatic differences in biofilm production, with strong producers yielding five times more biofilm than the weakest producers. IMPORTANCE Through an integration of metagenomic and experimental approaches, our work reveals the diversity and nature of interactions among key taxa in kombucha microbiomes through the construction of synthetic microbial pairs. Manipulation of these microbes in kombucha has the potential to shape both the fermentation qualities of kombucha and the production of biofilms and is valuable for kombucha beverage producers, biofilm engineers, and synthetic ecologists. |
format | Online Article Text |
id | pubmed-9238417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-92384172022-06-29 Microbial Diversity and Interaction Specificity in Kombucha Tea Fermentations Landis, Elizabeth A. Fogarty, Emily Edwards, John C. Popa, Otilia Eren, A. Murat Wolfe, Benjamin E. mSystems Research Article Despite the popularity of kombucha tea, the distribution of different microbes across kombucha ferments and how those microbes interact within communities are not well characterized. Using metagenomics, comparative genomics, synthetic community experiments, and metabolomics, we determined the taxonomic, ecological, and functional diversity of 23 distinct kombuchas from across the United States. Shotgun metagenomic sequencing demonstrated that the bacterium Komagataeibacter rhaeticus and the yeast Brettanomyces bruxellensis were the most common microbes in the sampled kombucha communities. To determine the specificity of bacterium-yeast interactions, we experimentally quantified microbial interactions within kombucha biofilms by measuring densities of interacting species and biofilm production. In pairwise combinations of bacteria and yeast, B. bruxellensis and individual strains of Komagataeibacter spp. were sufficient to form kombucha fermentations with robust biofilms, but Zygosaccharomyces bisporus, another yeast found in kombucha, did not stimulate bacteria to produce biofilms. Profiling the spent media of both yeast species using nuclear magnetic resonance spectroscopy suggested that the enhanced ability of B. bruxellensis to ferment and produce key metabolites in sucrose-sweetened tea may explain why it stimulates biofilm formation. Comparative genomics demonstrated that Komagataeibacter spp. with >99% genomic similarity can still have dramatic differences in biofilm production, with strong producers yielding five times more biofilm than the weakest producers. IMPORTANCE Through an integration of metagenomic and experimental approaches, our work reveals the diversity and nature of interactions among key taxa in kombucha microbiomes through the construction of synthetic microbial pairs. Manipulation of these microbes in kombucha has the potential to shape both the fermentation qualities of kombucha and the production of biofilms and is valuable for kombucha beverage producers, biofilm engineers, and synthetic ecologists. American Society for Microbiology 2022-06-07 /pmc/articles/PMC9238417/ /pubmed/35670539 http://dx.doi.org/10.1128/msystems.00157-22 Text en Copyright © 2022 Landis 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 Landis, Elizabeth A. Fogarty, Emily Edwards, John C. Popa, Otilia Eren, A. Murat Wolfe, Benjamin E. Microbial Diversity and Interaction Specificity in Kombucha Tea Fermentations |
title | Microbial Diversity and Interaction Specificity in Kombucha Tea Fermentations |
title_full | Microbial Diversity and Interaction Specificity in Kombucha Tea Fermentations |
title_fullStr | Microbial Diversity and Interaction Specificity in Kombucha Tea Fermentations |
title_full_unstemmed | Microbial Diversity and Interaction Specificity in Kombucha Tea Fermentations |
title_short | Microbial Diversity and Interaction Specificity in Kombucha Tea Fermentations |
title_sort | microbial diversity and interaction specificity in kombucha tea fermentations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238417/ https://www.ncbi.nlm.nih.gov/pubmed/35670539 http://dx.doi.org/10.1128/msystems.00157-22 |
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