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Human-Gut Phages Harbor Sporulation Genes

Spore-forming bacteria are prevalent in mammalian guts and have implications for host health and nutrition. The production of dormant spores is thought to play an important role in the colonization, persistence, and transmission of these bacteria. Spore formation also modifies interactions among mic...

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Autores principales: Schwartz, Daniel A., Rodríguez-Ramos, Josué A., Shaffer, Michael, Flynn, Rory M., Daly, Rebecca A., Wrighton, Kelly C., Lennon, Jay T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294663/
https://www.ncbi.nlm.nih.gov/pubmed/37042671
http://dx.doi.org/10.1128/mbio.00182-23
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author Schwartz, Daniel A.
Rodríguez-Ramos, Josué A.
Shaffer, Michael
Flynn, Rory M.
Daly, Rebecca A.
Wrighton, Kelly C.
Lennon, Jay T.
author_facet Schwartz, Daniel A.
Rodríguez-Ramos, Josué A.
Shaffer, Michael
Flynn, Rory M.
Daly, Rebecca A.
Wrighton, Kelly C.
Lennon, Jay T.
author_sort Schwartz, Daniel A.
collection PubMed
description Spore-forming bacteria are prevalent in mammalian guts and have implications for host health and nutrition. The production of dormant spores is thought to play an important role in the colonization, persistence, and transmission of these bacteria. Spore formation also modifies interactions among microorganisms such as infection by phages. Recent studies suggest that phages may counter dormancy-mediated defense through the expression of phage-carried sporulation genes during infection, which can alter the transitions between active and inactive states. By mining genomes and gut-derived metagenomes, we identified sporulation genes that are preferentially carried by phages that infect spore-forming bacteria. These included genes involved in chromosome partitioning, DNA damage repair, and cell wall-associated functions. In addition, phages contained homologs of sporulation-specific transcription factors, notably spo0A, the master regulator of sporulation, which could allow phages to control the complex genetic network responsible for spore development. Our findings suggest that phages could influence the formation of bacterial spores with implications for the health of the human gut microbiome, as well as bacterial communities in other environments.
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spelling pubmed-102946632023-06-28 Human-Gut Phages Harbor Sporulation Genes Schwartz, Daniel A. Rodríguez-Ramos, Josué A. Shaffer, Michael Flynn, Rory M. Daly, Rebecca A. Wrighton, Kelly C. Lennon, Jay T. mBio Observation Spore-forming bacteria are prevalent in mammalian guts and have implications for host health and nutrition. The production of dormant spores is thought to play an important role in the colonization, persistence, and transmission of these bacteria. Spore formation also modifies interactions among microorganisms such as infection by phages. Recent studies suggest that phages may counter dormancy-mediated defense through the expression of phage-carried sporulation genes during infection, which can alter the transitions between active and inactive states. By mining genomes and gut-derived metagenomes, we identified sporulation genes that are preferentially carried by phages that infect spore-forming bacteria. These included genes involved in chromosome partitioning, DNA damage repair, and cell wall-associated functions. In addition, phages contained homologs of sporulation-specific transcription factors, notably spo0A, the master regulator of sporulation, which could allow phages to control the complex genetic network responsible for spore development. Our findings suggest that phages could influence the formation of bacterial spores with implications for the health of the human gut microbiome, as well as bacterial communities in other environments. American Society for Microbiology 2023-04-12 /pmc/articles/PMC10294663/ /pubmed/37042671 http://dx.doi.org/10.1128/mbio.00182-23 Text en Copyright © 2023 Schwartz 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 Observation
Schwartz, Daniel A.
Rodríguez-Ramos, Josué A.
Shaffer, Michael
Flynn, Rory M.
Daly, Rebecca A.
Wrighton, Kelly C.
Lennon, Jay T.
Human-Gut Phages Harbor Sporulation Genes
title Human-Gut Phages Harbor Sporulation Genes
title_full Human-Gut Phages Harbor Sporulation Genes
title_fullStr Human-Gut Phages Harbor Sporulation Genes
title_full_unstemmed Human-Gut Phages Harbor Sporulation Genes
title_short Human-Gut Phages Harbor Sporulation Genes
title_sort human-gut phages harbor sporulation genes
topic Observation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294663/
https://www.ncbi.nlm.nih.gov/pubmed/37042671
http://dx.doi.org/10.1128/mbio.00182-23
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