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Dynamics of plasmid-mediated niche invasion, immunity to invasion, and pheromone-inducible conjugation in the murine gastrointestinal tract
Microbial communities provide protection to their hosts by resisting pathogenic invasion. Microbial residents of a host often exclude subsequent colonizers, but this protection is not well understood. The Enterococcus faecalis plasmid pCF10, whose conjugative transfer functions are induced by a pept...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927478/ https://www.ncbi.nlm.nih.gov/pubmed/35296679 http://dx.doi.org/10.1038/s41467-022-29028-7 |
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author | Hirt, Helmut Greenwood-Quaintance, Kerryl E. Barnes, Aaron M. T. Karau, Melissa J. Till, Lisa M. Palzer, Elise Guan, Weihua VanNieuwenhze, Michael S. Kashyap, Purna C. Patel, Robin Dunny, Gary M. |
author_facet | Hirt, Helmut Greenwood-Quaintance, Kerryl E. Barnes, Aaron M. T. Karau, Melissa J. Till, Lisa M. Palzer, Elise Guan, Weihua VanNieuwenhze, Michael S. Kashyap, Purna C. Patel, Robin Dunny, Gary M. |
author_sort | Hirt, Helmut |
collection | PubMed |
description | Microbial communities provide protection to their hosts by resisting pathogenic invasion. Microbial residents of a host often exclude subsequent colonizers, but this protection is not well understood. The Enterococcus faecalis plasmid pCF10, whose conjugative transfer functions are induced by a peptide pheromone, efficiently transfers in the intestinal tract of mice. Here we show that an invading donor strain established in the gastrointestinal tract of mice harboring resident recipients, resulting in a stable, mixed population comprised of approximately 10% donors and 90% recipients. We also show that the plasmid-encoded surface protein PrgB (Aggregation Substance), enhanced donor invasion of resident recipients, and resistance of resident donors to invasion by recipients. Imaging of the gastrointestinal mucosa of mice infected with differentially labeled recipients and donors revealed pheromone induction within microcolonies harboring both strains in close proximity, suggesting that adherent microcolonies on the mucosal surface of the intestine comprise an important niche for cell-cell signaling and plasmid transfer. |
format | Online Article Text |
id | pubmed-8927478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89274782022-04-01 Dynamics of plasmid-mediated niche invasion, immunity to invasion, and pheromone-inducible conjugation in the murine gastrointestinal tract Hirt, Helmut Greenwood-Quaintance, Kerryl E. Barnes, Aaron M. T. Karau, Melissa J. Till, Lisa M. Palzer, Elise Guan, Weihua VanNieuwenhze, Michael S. Kashyap, Purna C. Patel, Robin Dunny, Gary M. Nat Commun Article Microbial communities provide protection to their hosts by resisting pathogenic invasion. Microbial residents of a host often exclude subsequent colonizers, but this protection is not well understood. The Enterococcus faecalis plasmid pCF10, whose conjugative transfer functions are induced by a peptide pheromone, efficiently transfers in the intestinal tract of mice. Here we show that an invading donor strain established in the gastrointestinal tract of mice harboring resident recipients, resulting in a stable, mixed population comprised of approximately 10% donors and 90% recipients. We also show that the plasmid-encoded surface protein PrgB (Aggregation Substance), enhanced donor invasion of resident recipients, and resistance of resident donors to invasion by recipients. Imaging of the gastrointestinal mucosa of mice infected with differentially labeled recipients and donors revealed pheromone induction within microcolonies harboring both strains in close proximity, suggesting that adherent microcolonies on the mucosal surface of the intestine comprise an important niche for cell-cell signaling and plasmid transfer. Nature Publishing Group UK 2022-03-16 /pmc/articles/PMC8927478/ /pubmed/35296679 http://dx.doi.org/10.1038/s41467-022-29028-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hirt, Helmut Greenwood-Quaintance, Kerryl E. Barnes, Aaron M. T. Karau, Melissa J. Till, Lisa M. Palzer, Elise Guan, Weihua VanNieuwenhze, Michael S. Kashyap, Purna C. Patel, Robin Dunny, Gary M. Dynamics of plasmid-mediated niche invasion, immunity to invasion, and pheromone-inducible conjugation in the murine gastrointestinal tract |
title | Dynamics of plasmid-mediated niche invasion, immunity to invasion, and pheromone-inducible conjugation in the murine gastrointestinal tract |
title_full | Dynamics of plasmid-mediated niche invasion, immunity to invasion, and pheromone-inducible conjugation in the murine gastrointestinal tract |
title_fullStr | Dynamics of plasmid-mediated niche invasion, immunity to invasion, and pheromone-inducible conjugation in the murine gastrointestinal tract |
title_full_unstemmed | Dynamics of plasmid-mediated niche invasion, immunity to invasion, and pheromone-inducible conjugation in the murine gastrointestinal tract |
title_short | Dynamics of plasmid-mediated niche invasion, immunity to invasion, and pheromone-inducible conjugation in the murine gastrointestinal tract |
title_sort | dynamics of plasmid-mediated niche invasion, immunity to invasion, and pheromone-inducible conjugation in the murine gastrointestinal tract |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927478/ https://www.ncbi.nlm.nih.gov/pubmed/35296679 http://dx.doi.org/10.1038/s41467-022-29028-7 |
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