Cargando…

Ethanolamine Signaling Promotes Salmonella Niche Recognition and Adaptation during Infection

Chemical and nutrient signaling are fundamental for all cellular processes, including interactions between the mammalian host and the microbiota, which have a significant impact on health and disease. Ethanolamine is an essential component of cell membranes and has profound signaling activity within...

Descripción completa

Detalles Bibliográficos
Autores principales: Anderson, Christopher J., Clark, David E., Adli, Mazhar, Kendall, Melissa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643982/
https://www.ncbi.nlm.nih.gov/pubmed/26565973
http://dx.doi.org/10.1371/journal.ppat.1005278
_version_ 1782400598018097152
author Anderson, Christopher J.
Clark, David E.
Adli, Mazhar
Kendall, Melissa M.
author_facet Anderson, Christopher J.
Clark, David E.
Adli, Mazhar
Kendall, Melissa M.
author_sort Anderson, Christopher J.
collection PubMed
description Chemical and nutrient signaling are fundamental for all cellular processes, including interactions between the mammalian host and the microbiota, which have a significant impact on health and disease. Ethanolamine is an essential component of cell membranes and has profound signaling activity within mammalian cells by modulating inflammatory responses and intestinal physiology. Here, we describe a virulence-regulating pathway in which the foodborne pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium) exploits ethanolamine signaling to recognize and adapt to distinct niches within the host. The bacterial transcription factor EutR promotes ethanolamine metabolism in the intestine, which enables S. Typhimurium to establish infection. Subsequently, EutR directly activates expression of the Salmonella pathogenicity island 2 in the intramacrophage environment, and thus augments intramacrophage survival. Moreover, EutR is critical for robust dissemination during mammalian infection. Our findings reveal that S. Typhimurium co-opts ethanolamine as a signal to coordinate metabolism and then virulence. Because the ability to sense ethanolamine is a conserved trait among pathogenic and commensal bacteria, our work indicates that ethanolamine signaling may be a key step in the localized adaptation of bacteria within their mammalian hosts.
format Online
Article
Text
id pubmed-4643982
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-46439822015-11-18 Ethanolamine Signaling Promotes Salmonella Niche Recognition and Adaptation during Infection Anderson, Christopher J. Clark, David E. Adli, Mazhar Kendall, Melissa M. PLoS Pathog Research Article Chemical and nutrient signaling are fundamental for all cellular processes, including interactions between the mammalian host and the microbiota, which have a significant impact on health and disease. Ethanolamine is an essential component of cell membranes and has profound signaling activity within mammalian cells by modulating inflammatory responses and intestinal physiology. Here, we describe a virulence-regulating pathway in which the foodborne pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium) exploits ethanolamine signaling to recognize and adapt to distinct niches within the host. The bacterial transcription factor EutR promotes ethanolamine metabolism in the intestine, which enables S. Typhimurium to establish infection. Subsequently, EutR directly activates expression of the Salmonella pathogenicity island 2 in the intramacrophage environment, and thus augments intramacrophage survival. Moreover, EutR is critical for robust dissemination during mammalian infection. Our findings reveal that S. Typhimurium co-opts ethanolamine as a signal to coordinate metabolism and then virulence. Because the ability to sense ethanolamine is a conserved trait among pathogenic and commensal bacteria, our work indicates that ethanolamine signaling may be a key step in the localized adaptation of bacteria within their mammalian hosts. Public Library of Science 2015-11-13 /pmc/articles/PMC4643982/ /pubmed/26565973 http://dx.doi.org/10.1371/journal.ppat.1005278 Text en © 2015 Anderson 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
Anderson, Christopher J.
Clark, David E.
Adli, Mazhar
Kendall, Melissa M.
Ethanolamine Signaling Promotes Salmonella Niche Recognition and Adaptation during Infection
title Ethanolamine Signaling Promotes Salmonella Niche Recognition and Adaptation during Infection
title_full Ethanolamine Signaling Promotes Salmonella Niche Recognition and Adaptation during Infection
title_fullStr Ethanolamine Signaling Promotes Salmonella Niche Recognition and Adaptation during Infection
title_full_unstemmed Ethanolamine Signaling Promotes Salmonella Niche Recognition and Adaptation during Infection
title_short Ethanolamine Signaling Promotes Salmonella Niche Recognition and Adaptation during Infection
title_sort ethanolamine signaling promotes salmonella niche recognition and adaptation during infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4643982/
https://www.ncbi.nlm.nih.gov/pubmed/26565973
http://dx.doi.org/10.1371/journal.ppat.1005278
work_keys_str_mv AT andersonchristopherj ethanolaminesignalingpromotessalmonellanicherecognitionandadaptationduringinfection
AT clarkdavide ethanolaminesignalingpromotessalmonellanicherecognitionandadaptationduringinfection
AT adlimazhar ethanolaminesignalingpromotessalmonellanicherecognitionandadaptationduringinfection
AT kendallmelissam ethanolaminesignalingpromotessalmonellanicherecognitionandadaptationduringinfection