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SinR Controls Enterotoxin Expression in Bacillus thuringiensis Biofilms

The entomopathogen Bacillus thuringiensis produces dense biofilms under various conditions. Here, we report that the transition phase regulators Spo0A, AbrB and SinR control biofilm formation and swimming motility in B. thuringiensis, just as they control biofilm formation and swarming motility in t...

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Autores principales: Fagerlund, Annette, Dubois, Thomas, Økstad, Ole-Andreas, Verplaetse, Emilie, Gilois, Nathalie, Bennaceur, Imène, Perchat, Stéphane, Gominet, Myriam, Aymerich, Stéphane, Kolstø, Anne-Brit, Lereclus, Didier, Gohar, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909190/
https://www.ncbi.nlm.nih.gov/pubmed/24498128
http://dx.doi.org/10.1371/journal.pone.0087532
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author Fagerlund, Annette
Dubois, Thomas
Økstad, Ole-Andreas
Verplaetse, Emilie
Gilois, Nathalie
Bennaceur, Imène
Perchat, Stéphane
Gominet, Myriam
Aymerich, Stéphane
Kolstø, Anne-Brit
Lereclus, Didier
Gohar, Michel
author_facet Fagerlund, Annette
Dubois, Thomas
Økstad, Ole-Andreas
Verplaetse, Emilie
Gilois, Nathalie
Bennaceur, Imène
Perchat, Stéphane
Gominet, Myriam
Aymerich, Stéphane
Kolstø, Anne-Brit
Lereclus, Didier
Gohar, Michel
author_sort Fagerlund, Annette
collection PubMed
description The entomopathogen Bacillus thuringiensis produces dense biofilms under various conditions. Here, we report that the transition phase regulators Spo0A, AbrB and SinR control biofilm formation and swimming motility in B. thuringiensis, just as they control biofilm formation and swarming motility in the closely related saprophyte species B. subtilis. However, microarray analysis indicated that in B. thuringiensis, in contrast to B. subtilis, SinR does not control an eps operon involved in exopolysaccharides production, but regulates genes involved in the biosynthesis of the lipopeptide kurstakin. This lipopeptide is required for biofilm formation and was previously shown to be important for survival in the host cadaver (necrotrophism). Microarray analysis also revealed that the SinR regulon contains genes coding for the Hbl enterotoxin. Transcriptional fusion assays, Western blots and hemolysis assays confirmed that SinR controls Hbl expression, together with PlcR, the main virulence regulator in B. thuringiensis. We show that Hbl is expressed in a sustained way in a small subpopulation of the biofilm, whereas almost all the planktonic population transiently expresses Hbl. The gene coding for SinI, an antagonist of SinR, is expressed in the same biofilm subpopulation as hbl, suggesting that hbl transcription heterogeneity is SinI-dependent. B. thuringiensis and B. cereus are enteric bacteria which possibly form biofilms lining the host intestinal epithelium. Toxins produced in biofilms could therefore be delivered directly to the target tissue.
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spelling pubmed-39091902014-02-04 SinR Controls Enterotoxin Expression in Bacillus thuringiensis Biofilms Fagerlund, Annette Dubois, Thomas Økstad, Ole-Andreas Verplaetse, Emilie Gilois, Nathalie Bennaceur, Imène Perchat, Stéphane Gominet, Myriam Aymerich, Stéphane Kolstø, Anne-Brit Lereclus, Didier Gohar, Michel PLoS One Research Article The entomopathogen Bacillus thuringiensis produces dense biofilms under various conditions. Here, we report that the transition phase regulators Spo0A, AbrB and SinR control biofilm formation and swimming motility in B. thuringiensis, just as they control biofilm formation and swarming motility in the closely related saprophyte species B. subtilis. However, microarray analysis indicated that in B. thuringiensis, in contrast to B. subtilis, SinR does not control an eps operon involved in exopolysaccharides production, but regulates genes involved in the biosynthesis of the lipopeptide kurstakin. This lipopeptide is required for biofilm formation and was previously shown to be important for survival in the host cadaver (necrotrophism). Microarray analysis also revealed that the SinR regulon contains genes coding for the Hbl enterotoxin. Transcriptional fusion assays, Western blots and hemolysis assays confirmed that SinR controls Hbl expression, together with PlcR, the main virulence regulator in B. thuringiensis. We show that Hbl is expressed in a sustained way in a small subpopulation of the biofilm, whereas almost all the planktonic population transiently expresses Hbl. The gene coding for SinI, an antagonist of SinR, is expressed in the same biofilm subpopulation as hbl, suggesting that hbl transcription heterogeneity is SinI-dependent. B. thuringiensis and B. cereus are enteric bacteria which possibly form biofilms lining the host intestinal epithelium. Toxins produced in biofilms could therefore be delivered directly to the target tissue. Public Library of Science 2014-01-31 /pmc/articles/PMC3909190/ /pubmed/24498128 http://dx.doi.org/10.1371/journal.pone.0087532 Text en © 2014 Fagerlund et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fagerlund, Annette
Dubois, Thomas
Økstad, Ole-Andreas
Verplaetse, Emilie
Gilois, Nathalie
Bennaceur, Imène
Perchat, Stéphane
Gominet, Myriam
Aymerich, Stéphane
Kolstø, Anne-Brit
Lereclus, Didier
Gohar, Michel
SinR Controls Enterotoxin Expression in Bacillus thuringiensis Biofilms
title SinR Controls Enterotoxin Expression in Bacillus thuringiensis Biofilms
title_full SinR Controls Enterotoxin Expression in Bacillus thuringiensis Biofilms
title_fullStr SinR Controls Enterotoxin Expression in Bacillus thuringiensis Biofilms
title_full_unstemmed SinR Controls Enterotoxin Expression in Bacillus thuringiensis Biofilms
title_short SinR Controls Enterotoxin Expression in Bacillus thuringiensis Biofilms
title_sort sinr controls enterotoxin expression in bacillus thuringiensis biofilms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909190/
https://www.ncbi.nlm.nih.gov/pubmed/24498128
http://dx.doi.org/10.1371/journal.pone.0087532
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