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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...

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Autores principales: Landis, Elizabeth A., Fogarty, Emily, Edwards, John C., Popa, Otilia, Eren, A. Murat, Wolfe, Benjamin E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
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.
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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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