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Temperature-regulated heterogeneous extracellular matrix gene expression defines biofilm morphology in Clostridium perfringens
Cells in biofilms dynamically adapt to surrounding environmental conditions, which alters biofilm architecture. The obligate anaerobic pathogen Clostridium perfringens shows different biofilm structures in different temperatures. Here we find that the temperature-regulated production of extracellula...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395162/ https://www.ncbi.nlm.nih.gov/pubmed/32737303 http://dx.doi.org/10.1038/s41522-020-00139-7 |
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author | Obana, Nozomu Nakamura, Kouji Nomura, Nobuhiko |
author_facet | Obana, Nozomu Nakamura, Kouji Nomura, Nobuhiko |
author_sort | Obana, Nozomu |
collection | PubMed |
description | Cells in biofilms dynamically adapt to surrounding environmental conditions, which alters biofilm architecture. The obligate anaerobic pathogen Clostridium perfringens shows different biofilm structures in different temperatures. Here we find that the temperature-regulated production of extracellular polymeric substance (EPS) is necessary for morphological changes in biofilms. We identify BsaA proteins as an EPS matrix necessary for pellicle biofilm formation at lower temperature and find that extracellularly secreted BsaA protein forms filamentous polymers. We show that sipW-bsaA operon expression is bimodal, and the EPS-producing population size is increased at a lower temperature. This heterogeneous expression of the EPS gene requires a two-component system. We find that EPS-producing cells cover EPS-nonproducing cells attaching to the bottom surface. In the deletion mutant of pilA2, encoding a type IV pilin, the EPS gene expression is ON in the whole population. This heterogeneity is further regulated by the cleavage of the pilA2 mRNA by RNase Y, causing temperature-responsive EPS expression in biofilms. As temperature is an environmental cue, C. perfringens may modulate EPS expression to induce morphological changes in biofilm structure as a strategy for adapting to interhost and external environments. |
format | Online Article Text |
id | pubmed-7395162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73951622020-08-18 Temperature-regulated heterogeneous extracellular matrix gene expression defines biofilm morphology in Clostridium perfringens Obana, Nozomu Nakamura, Kouji Nomura, Nobuhiko NPJ Biofilms Microbiomes Article Cells in biofilms dynamically adapt to surrounding environmental conditions, which alters biofilm architecture. The obligate anaerobic pathogen Clostridium perfringens shows different biofilm structures in different temperatures. Here we find that the temperature-regulated production of extracellular polymeric substance (EPS) is necessary for morphological changes in biofilms. We identify BsaA proteins as an EPS matrix necessary for pellicle biofilm formation at lower temperature and find that extracellularly secreted BsaA protein forms filamentous polymers. We show that sipW-bsaA operon expression is bimodal, and the EPS-producing population size is increased at a lower temperature. This heterogeneous expression of the EPS gene requires a two-component system. We find that EPS-producing cells cover EPS-nonproducing cells attaching to the bottom surface. In the deletion mutant of pilA2, encoding a type IV pilin, the EPS gene expression is ON in the whole population. This heterogeneity is further regulated by the cleavage of the pilA2 mRNA by RNase Y, causing temperature-responsive EPS expression in biofilms. As temperature is an environmental cue, C. perfringens may modulate EPS expression to induce morphological changes in biofilm structure as a strategy for adapting to interhost and external environments. Nature Publishing Group UK 2020-07-31 /pmc/articles/PMC7395162/ /pubmed/32737303 http://dx.doi.org/10.1038/s41522-020-00139-7 Text en © The Author(s) 2020 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 Obana, Nozomu Nakamura, Kouji Nomura, Nobuhiko Temperature-regulated heterogeneous extracellular matrix gene expression defines biofilm morphology in Clostridium perfringens |
title | Temperature-regulated heterogeneous extracellular matrix gene expression defines biofilm morphology in Clostridium perfringens |
title_full | Temperature-regulated heterogeneous extracellular matrix gene expression defines biofilm morphology in Clostridium perfringens |
title_fullStr | Temperature-regulated heterogeneous extracellular matrix gene expression defines biofilm morphology in Clostridium perfringens |
title_full_unstemmed | Temperature-regulated heterogeneous extracellular matrix gene expression defines biofilm morphology in Clostridium perfringens |
title_short | Temperature-regulated heterogeneous extracellular matrix gene expression defines biofilm morphology in Clostridium perfringens |
title_sort | temperature-regulated heterogeneous extracellular matrix gene expression defines biofilm morphology in clostridium perfringens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395162/ https://www.ncbi.nlm.nih.gov/pubmed/32737303 http://dx.doi.org/10.1038/s41522-020-00139-7 |
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