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A mechanical signal transmitted by the flagellum controls signalling in Bacillus subtilis

In the natural environment bacteria predominantly live adhered to a surface as part of a biofilm. While many of the components needed for biofilm assembly are known, the mechanism by which microbes sense and respond to contact with a surface is poorly understood. Bacillus subtilis is a Gram-positive...

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Autores principales: Cairns, Lynne S, Marlow, Victoria L, Bissett, Emma, Ostrowski, Adam, Stanley-Wall, Nicola R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963450/
https://www.ncbi.nlm.nih.gov/pubmed/23888912
http://dx.doi.org/10.1111/mmi.12342
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author Cairns, Lynne S
Marlow, Victoria L
Bissett, Emma
Ostrowski, Adam
Stanley-Wall, Nicola R
author_facet Cairns, Lynne S
Marlow, Victoria L
Bissett, Emma
Ostrowski, Adam
Stanley-Wall, Nicola R
author_sort Cairns, Lynne S
collection PubMed
description In the natural environment bacteria predominantly live adhered to a surface as part of a biofilm. While many of the components needed for biofilm assembly are known, the mechanism by which microbes sense and respond to contact with a surface is poorly understood. Bacillus subtilis is a Gram-positive model for biofilm formation. The DegS–DegU two-component system controls several multicellular behaviours in B. subtilis, including biofilm formation. Here we identify the B. subtilis flagellum as a mechanosensor that activates the DegS–DegU regulatory pathway. Inhibition of flagellar rotation by deletion or mutation of the flagellar stator gene, motB, results in an increase in both degU transcription and DegU∼P driven processes, namely exoprotease production and poly-γ-dl-glutamic acid biosynthesis. Similarly, inhibition of flagellar rotation by engaging the flagellar clutch or by tethering the flagella with antibodies also promotes an increase in degU transcription that is reflective of increased DegU∼P levels in the cell. Collectively, these findings strongly indicate that inhibition of flagellar rotation acts as a mechanical trigger to activate the DegS–DegU two-component signal transduction system. We postulate that inhibition of flagellar rotation could function as a mechanical trigger to activate bacterial signal transduction cascades in many motile bacteria upon contact with a surface.
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spelling pubmed-39634502014-03-25 A mechanical signal transmitted by the flagellum controls signalling in Bacillus subtilis Cairns, Lynne S Marlow, Victoria L Bissett, Emma Ostrowski, Adam Stanley-Wall, Nicola R Mol Microbiol Research Articles In the natural environment bacteria predominantly live adhered to a surface as part of a biofilm. While many of the components needed for biofilm assembly are known, the mechanism by which microbes sense and respond to contact with a surface is poorly understood. Bacillus subtilis is a Gram-positive model for biofilm formation. The DegS–DegU two-component system controls several multicellular behaviours in B. subtilis, including biofilm formation. Here we identify the B. subtilis flagellum as a mechanosensor that activates the DegS–DegU regulatory pathway. Inhibition of flagellar rotation by deletion or mutation of the flagellar stator gene, motB, results in an increase in both degU transcription and DegU∼P driven processes, namely exoprotease production and poly-γ-dl-glutamic acid biosynthesis. Similarly, inhibition of flagellar rotation by engaging the flagellar clutch or by tethering the flagella with antibodies also promotes an increase in degU transcription that is reflective of increased DegU∼P levels in the cell. Collectively, these findings strongly indicate that inhibition of flagellar rotation acts as a mechanical trigger to activate the DegS–DegU two-component signal transduction system. We postulate that inhibition of flagellar rotation could function as a mechanical trigger to activate bacterial signal transduction cascades in many motile bacteria upon contact with a surface. John Wiley & Sons Ltd 2013-10 2013-08-14 /pmc/articles/PMC3963450/ /pubmed/23888912 http://dx.doi.org/10.1111/mmi.12342 Text en © 2013 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Cairns, Lynne S
Marlow, Victoria L
Bissett, Emma
Ostrowski, Adam
Stanley-Wall, Nicola R
A mechanical signal transmitted by the flagellum controls signalling in Bacillus subtilis
title A mechanical signal transmitted by the flagellum controls signalling in Bacillus subtilis
title_full A mechanical signal transmitted by the flagellum controls signalling in Bacillus subtilis
title_fullStr A mechanical signal transmitted by the flagellum controls signalling in Bacillus subtilis
title_full_unstemmed A mechanical signal transmitted by the flagellum controls signalling in Bacillus subtilis
title_short A mechanical signal transmitted by the flagellum controls signalling in Bacillus subtilis
title_sort mechanical signal transmitted by the flagellum controls signalling in bacillus subtilis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963450/
https://www.ncbi.nlm.nih.gov/pubmed/23888912
http://dx.doi.org/10.1111/mmi.12342
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