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Spontaneous mutations in the flhD operon generate motility heterogeneity in Escherichia coli biofilm

BACKGROUND: Heterogeneity and niche adaptation in bacterial biofilm involve changes to the genetic makeup of the bacteria and gene expression control. We hypothesized that i) spontaneous mutations in the flhD operon can either increase or decrease motility and that ii) the resulting motility heterog...

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Autores principales: Horne, Shelley M., Sayler, Joseph, Scarberry, Nicholas, Schroeder, Meredith, Lynnes, Ty, Prüß, Birgit M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100188/
https://www.ncbi.nlm.nih.gov/pubmed/27821046
http://dx.doi.org/10.1186/s12866-016-0878-1
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author Horne, Shelley M.
Sayler, Joseph
Scarberry, Nicholas
Schroeder, Meredith
Lynnes, Ty
Prüß, Birgit M.
author_facet Horne, Shelley M.
Sayler, Joseph
Scarberry, Nicholas
Schroeder, Meredith
Lynnes, Ty
Prüß, Birgit M.
author_sort Horne, Shelley M.
collection PubMed
description BACKGROUND: Heterogeneity and niche adaptation in bacterial biofilm involve changes to the genetic makeup of the bacteria and gene expression control. We hypothesized that i) spontaneous mutations in the flhD operon can either increase or decrease motility and that ii) the resulting motility heterogeneity in the biofilm might lead to a long-term increase in biofilm biomass. RESULTS: We allowed the highly motile E. coli K-12 strain MC1000 to form seven- and fourteen-day old biofilm, from which we recovered reduced motility isolates at a substantially greater frequency (5.4 %) than from a similar experiment with planktonic bacteria (0.1 %). Biofilms formed exclusively by MC1000 degraded after 2 weeks. In contrast, biofilms initiated with a 1:1 ratio of MC1000 and its isogenic flhD::kn mutant remained intact at 4 weeks and the two strains remained in equilibrium for at least two weeks. These data imply that an ‘optimal’ biofilm may contain a mixture of motile and non-motile bacteria. Twenty-eight of the non-motile MC1000 isolates contained an IS1 element in proximity to the translational start of FlhD or within the open reading frames for FlhD or FlhC. Two isolates had an IS2 and one isolate had an IS5 in the open reading frame for FlhD. An additional three isolates contained deletions that included the RNA polymerase binding site, five isolates contained point mutations and small deletions in the open reading frame for FlhC. The locations of all these mutations are consistent with the lack of motility and further downstream within the flhD operon than previously published IS elements that increased motility. We believe that the location of the mutation within the flhD operon determines whether the effect on motility is positive or negative. To test the second part of our hypothesis where motility heterogeneity in a biofilm may lead to a long-term increase in biofilm biomass, we quantified biofilm biomass by MC1000, MC1000 flhD::kn, and mixtures of the two strains at ratios of 1:1, 10:1, and 1:10. After 3 weeks, biofilm of the mixed cultures contained up to five times more biomass than biofilm of each of the individual strains. CONCLUSION: Mutations in the flhD operon can exert positive or negative effects on motility, depending on the site of the mutation. We believe that this is a mechanism to generate motility heterogeneity within E. coli biofilm, which may help to maintain biofilm biomass over extended periods of time. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0878-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-51001882016-11-08 Spontaneous mutations in the flhD operon generate motility heterogeneity in Escherichia coli biofilm Horne, Shelley M. Sayler, Joseph Scarberry, Nicholas Schroeder, Meredith Lynnes, Ty Prüß, Birgit M. BMC Microbiol Research Article BACKGROUND: Heterogeneity and niche adaptation in bacterial biofilm involve changes to the genetic makeup of the bacteria and gene expression control. We hypothesized that i) spontaneous mutations in the flhD operon can either increase or decrease motility and that ii) the resulting motility heterogeneity in the biofilm might lead to a long-term increase in biofilm biomass. RESULTS: We allowed the highly motile E. coli K-12 strain MC1000 to form seven- and fourteen-day old biofilm, from which we recovered reduced motility isolates at a substantially greater frequency (5.4 %) than from a similar experiment with planktonic bacteria (0.1 %). Biofilms formed exclusively by MC1000 degraded after 2 weeks. In contrast, biofilms initiated with a 1:1 ratio of MC1000 and its isogenic flhD::kn mutant remained intact at 4 weeks and the two strains remained in equilibrium for at least two weeks. These data imply that an ‘optimal’ biofilm may contain a mixture of motile and non-motile bacteria. Twenty-eight of the non-motile MC1000 isolates contained an IS1 element in proximity to the translational start of FlhD or within the open reading frames for FlhD or FlhC. Two isolates had an IS2 and one isolate had an IS5 in the open reading frame for FlhD. An additional three isolates contained deletions that included the RNA polymerase binding site, five isolates contained point mutations and small deletions in the open reading frame for FlhC. The locations of all these mutations are consistent with the lack of motility and further downstream within the flhD operon than previously published IS elements that increased motility. We believe that the location of the mutation within the flhD operon determines whether the effect on motility is positive or negative. To test the second part of our hypothesis where motility heterogeneity in a biofilm may lead to a long-term increase in biofilm biomass, we quantified biofilm biomass by MC1000, MC1000 flhD::kn, and mixtures of the two strains at ratios of 1:1, 10:1, and 1:10. After 3 weeks, biofilm of the mixed cultures contained up to five times more biomass than biofilm of each of the individual strains. CONCLUSION: Mutations in the flhD operon can exert positive or negative effects on motility, depending on the site of the mutation. We believe that this is a mechanism to generate motility heterogeneity within E. coli biofilm, which may help to maintain biofilm biomass over extended periods of time. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0878-1) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-08 /pmc/articles/PMC5100188/ /pubmed/27821046 http://dx.doi.org/10.1186/s12866-016-0878-1 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Horne, Shelley M.
Sayler, Joseph
Scarberry, Nicholas
Schroeder, Meredith
Lynnes, Ty
Prüß, Birgit M.
Spontaneous mutations in the flhD operon generate motility heterogeneity in Escherichia coli biofilm
title Spontaneous mutations in the flhD operon generate motility heterogeneity in Escherichia coli biofilm
title_full Spontaneous mutations in the flhD operon generate motility heterogeneity in Escherichia coli biofilm
title_fullStr Spontaneous mutations in the flhD operon generate motility heterogeneity in Escherichia coli biofilm
title_full_unstemmed Spontaneous mutations in the flhD operon generate motility heterogeneity in Escherichia coli biofilm
title_short Spontaneous mutations in the flhD operon generate motility heterogeneity in Escherichia coli biofilm
title_sort spontaneous mutations in the flhd operon generate motility heterogeneity in escherichia coli biofilm
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100188/
https://www.ncbi.nlm.nih.gov/pubmed/27821046
http://dx.doi.org/10.1186/s12866-016-0878-1
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