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Zinc–induced envelope stress diminishes type III secretion in enteropathogenic Escherichia coli

BACKGROUND: Dietary supplementation with zinc has been shown to reduce the duration and severity of diarrhoeal disease caused by Enteropathogenic Escherichia coli, common in infants in developing countries. Initially this therapeutic benefit was attributed to the correction of zinc deficiency in mal...

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Autores principales: Mellies, Jay L, Thomas, Katherine, Turvey, Michael, Evans, Neil R, Crane, John, Boedeker, Ed, Benison, Gregory C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3438133/
https://www.ncbi.nlm.nih.gov/pubmed/22727253
http://dx.doi.org/10.1186/1471-2180-12-123
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author Mellies, Jay L
Thomas, Katherine
Turvey, Michael
Evans, Neil R
Crane, John
Boedeker, Ed
Benison, Gregory C
author_facet Mellies, Jay L
Thomas, Katherine
Turvey, Michael
Evans, Neil R
Crane, John
Boedeker, Ed
Benison, Gregory C
author_sort Mellies, Jay L
collection PubMed
description BACKGROUND: Dietary supplementation with zinc has been shown to reduce the duration and severity of diarrhoeal disease caused by Enteropathogenic Escherichia coli, common in infants in developing countries. Initially this therapeutic benefit was attributed to the correction of zinc deficiency in malnourished individuals, but recently evidence has emerged that zinc significantly impacts the pathogens themselves: zinc concentrations achievable by oral supplementation can reduce the expression of key virulence-related genes in EPEC and related organisms. RESULTS: Here, we investigate three possible mechanisms for such zinc-induced changes in expression of EPEC virulence: direct interaction of zinc with regulators of LEE operons; genetic interaction of LEE operons with known regulators of zinc homeostasis; and finally, downregulation of LEE transcription associated with activation of the σ(E)envelope stress response by zinc. We find evidence only for the latter mechanism, including zinc-induced down-regulation of type III secretion in EPEC similar to that caused by ammonium metavanadate, another known inducer of the σ(E)stress response. CONCLUSIONS: We conclude therefore that envelope stress is a major mechanism by which zinc attenuates the virulence of EPEC and related pathogens.
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spelling pubmed-34381332012-09-11 Zinc–induced envelope stress diminishes type III secretion in enteropathogenic Escherichia coli Mellies, Jay L Thomas, Katherine Turvey, Michael Evans, Neil R Crane, John Boedeker, Ed Benison, Gregory C BMC Microbiol Research Article BACKGROUND: Dietary supplementation with zinc has been shown to reduce the duration and severity of diarrhoeal disease caused by Enteropathogenic Escherichia coli, common in infants in developing countries. Initially this therapeutic benefit was attributed to the correction of zinc deficiency in malnourished individuals, but recently evidence has emerged that zinc significantly impacts the pathogens themselves: zinc concentrations achievable by oral supplementation can reduce the expression of key virulence-related genes in EPEC and related organisms. RESULTS: Here, we investigate three possible mechanisms for such zinc-induced changes in expression of EPEC virulence: direct interaction of zinc with regulators of LEE operons; genetic interaction of LEE operons with known regulators of zinc homeostasis; and finally, downregulation of LEE transcription associated with activation of the σ(E)envelope stress response by zinc. We find evidence only for the latter mechanism, including zinc-induced down-regulation of type III secretion in EPEC similar to that caused by ammonium metavanadate, another known inducer of the σ(E)stress response. CONCLUSIONS: We conclude therefore that envelope stress is a major mechanism by which zinc attenuates the virulence of EPEC and related pathogens. BioMed Central 2012-06-24 /pmc/articles/PMC3438133/ /pubmed/22727253 http://dx.doi.org/10.1186/1471-2180-12-123 Text en Copyright ©2012 Mellies et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mellies, Jay L
Thomas, Katherine
Turvey, Michael
Evans, Neil R
Crane, John
Boedeker, Ed
Benison, Gregory C
Zinc–induced envelope stress diminishes type III secretion in enteropathogenic Escherichia coli
title Zinc–induced envelope stress diminishes type III secretion in enteropathogenic Escherichia coli
title_full Zinc–induced envelope stress diminishes type III secretion in enteropathogenic Escherichia coli
title_fullStr Zinc–induced envelope stress diminishes type III secretion in enteropathogenic Escherichia coli
title_full_unstemmed Zinc–induced envelope stress diminishes type III secretion in enteropathogenic Escherichia coli
title_short Zinc–induced envelope stress diminishes type III secretion in enteropathogenic Escherichia coli
title_sort zinc–induced envelope stress diminishes type iii secretion in enteropathogenic escherichia coli
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3438133/
https://www.ncbi.nlm.nih.gov/pubmed/22727253
http://dx.doi.org/10.1186/1471-2180-12-123
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