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Phase and antigenic variation govern competition dynamics through positioning in bacterial colonies
Cellular positioning towards the surface of bacterial colonies and biofilms can enhance dispersal, provide a selective advantage due to increased nutrient and space availability, or shield interior cells from external stresses. Little is known about the molecular mechanisms that govern bacterial pos...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610331/ https://www.ncbi.nlm.nih.gov/pubmed/28939833 http://dx.doi.org/10.1038/s41598-017-12472-7 |
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author | Zöllner, Robert Oldewurtel, Enno R. Kouzel, Nadzeya Maier, Berenike |
author_facet | Zöllner, Robert Oldewurtel, Enno R. Kouzel, Nadzeya Maier, Berenike |
author_sort | Zöllner, Robert |
collection | PubMed |
description | Cellular positioning towards the surface of bacterial colonies and biofilms can enhance dispersal, provide a selective advantage due to increased nutrient and space availability, or shield interior cells from external stresses. Little is known about the molecular mechanisms that govern bacterial positioning. Using the type IV pilus (T4P) of Neisseria gonorrhoeae, we tested the hypothesis that the processes of phase and antigenic variation govern positioning and thus enhance bacterial fitness in expanding gonococcal colonies. By independently tuning growth rate and T4P-mediated interaction forces, we show that the loss of T4P and the subsequent segregation to the front confers a strong selective advantage. Sequencing of the major pilin gene of the spatially segregated sub-populations and an investigation of the spatio-temporal population dynamics was carried out. Our findings indicate that pilin phase and antigenic variation generate a standing variation of pilin sequences within the inoculation zone, while variants associated with a non-piliated phenotype segregate to the front of the growing colony. We conclude that tuning of attractive forces by phase and antigenic variation is a powerful mechanism for governing the dynamics of bacterial colonies. |
format | Online Article Text |
id | pubmed-5610331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56103312017-10-10 Phase and antigenic variation govern competition dynamics through positioning in bacterial colonies Zöllner, Robert Oldewurtel, Enno R. Kouzel, Nadzeya Maier, Berenike Sci Rep Article Cellular positioning towards the surface of bacterial colonies and biofilms can enhance dispersal, provide a selective advantage due to increased nutrient and space availability, or shield interior cells from external stresses. Little is known about the molecular mechanisms that govern bacterial positioning. Using the type IV pilus (T4P) of Neisseria gonorrhoeae, we tested the hypothesis that the processes of phase and antigenic variation govern positioning and thus enhance bacterial fitness in expanding gonococcal colonies. By independently tuning growth rate and T4P-mediated interaction forces, we show that the loss of T4P and the subsequent segregation to the front confers a strong selective advantage. Sequencing of the major pilin gene of the spatially segregated sub-populations and an investigation of the spatio-temporal population dynamics was carried out. Our findings indicate that pilin phase and antigenic variation generate a standing variation of pilin sequences within the inoculation zone, while variants associated with a non-piliated phenotype segregate to the front of the growing colony. We conclude that tuning of attractive forces by phase and antigenic variation is a powerful mechanism for governing the dynamics of bacterial colonies. Nature Publishing Group UK 2017-09-22 /pmc/articles/PMC5610331/ /pubmed/28939833 http://dx.doi.org/10.1038/s41598-017-12472-7 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Zöllner, Robert Oldewurtel, Enno R. Kouzel, Nadzeya Maier, Berenike Phase and antigenic variation govern competition dynamics through positioning in bacterial colonies |
title | Phase and antigenic variation govern competition dynamics through positioning in bacterial colonies |
title_full | Phase and antigenic variation govern competition dynamics through positioning in bacterial colonies |
title_fullStr | Phase and antigenic variation govern competition dynamics through positioning in bacterial colonies |
title_full_unstemmed | Phase and antigenic variation govern competition dynamics through positioning in bacterial colonies |
title_short | Phase and antigenic variation govern competition dynamics through positioning in bacterial colonies |
title_sort | phase and antigenic variation govern competition dynamics through positioning in bacterial colonies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610331/ https://www.ncbi.nlm.nih.gov/pubmed/28939833 http://dx.doi.org/10.1038/s41598-017-12472-7 |
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