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A Highly Conserved Bacterial D-Serine Uptake System Links Host Metabolism and Virulence

The ability of any organism to sense and respond to challenges presented in the environment is critically important for promoting or restricting colonization of specific sites. Recent work has demonstrated that the host metabolite D-serine has the ability to markedly influence the outcome of infecti...

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Autores principales: Connolly, James P. R., Gabrielsen, Mads, Goldstone, Robert J., Grinter, Rhys, Wang, Dai, Cogdell, Richard J., Walker, Daniel, Smith, David G. E., Roe, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4699771/
https://www.ncbi.nlm.nih.gov/pubmed/26727373
http://dx.doi.org/10.1371/journal.ppat.1005359
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author Connolly, James P. R.
Gabrielsen, Mads
Goldstone, Robert J.
Grinter, Rhys
Wang, Dai
Cogdell, Richard J.
Walker, Daniel
Smith, David G. E.
Roe, Andrew J.
author_facet Connolly, James P. R.
Gabrielsen, Mads
Goldstone, Robert J.
Grinter, Rhys
Wang, Dai
Cogdell, Richard J.
Walker, Daniel
Smith, David G. E.
Roe, Andrew J.
author_sort Connolly, James P. R.
collection PubMed
description The ability of any organism to sense and respond to challenges presented in the environment is critically important for promoting or restricting colonization of specific sites. Recent work has demonstrated that the host metabolite D-serine has the ability to markedly influence the outcome of infection by repressing the type III secretion system of enterohaemorrhagic Escherichia coli (EHEC) in a concentration-dependent manner. However, exactly how EHEC monitors environmental D-serine is not understood. In this work, we have identified two highly conserved members of the E. coli core genome, encoding an inner membrane transporter and a transcriptional regulator, which collectively help to “sense” levels of D-serine by regulating its uptake from the environment and in turn influencing global gene expression. Both proteins are required for full expression of the type III secretion system and diversely regulated prophage-encoded effector proteins demonstrating an important infection-relevant adaptation of the core genome. We propose that this system acts as a key safety net, sampling the environment for this metabolite, thereby promoting colonization of EHEC to favorable sites within the host.
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spelling pubmed-46997712016-01-15 A Highly Conserved Bacterial D-Serine Uptake System Links Host Metabolism and Virulence Connolly, James P. R. Gabrielsen, Mads Goldstone, Robert J. Grinter, Rhys Wang, Dai Cogdell, Richard J. Walker, Daniel Smith, David G. E. Roe, Andrew J. PLoS Pathog Research Article The ability of any organism to sense and respond to challenges presented in the environment is critically important for promoting or restricting colonization of specific sites. Recent work has demonstrated that the host metabolite D-serine has the ability to markedly influence the outcome of infection by repressing the type III secretion system of enterohaemorrhagic Escherichia coli (EHEC) in a concentration-dependent manner. However, exactly how EHEC monitors environmental D-serine is not understood. In this work, we have identified two highly conserved members of the E. coli core genome, encoding an inner membrane transporter and a transcriptional regulator, which collectively help to “sense” levels of D-serine by regulating its uptake from the environment and in turn influencing global gene expression. Both proteins are required for full expression of the type III secretion system and diversely regulated prophage-encoded effector proteins demonstrating an important infection-relevant adaptation of the core genome. We propose that this system acts as a key safety net, sampling the environment for this metabolite, thereby promoting colonization of EHEC to favorable sites within the host. Public Library of Science 2016-01-04 /pmc/articles/PMC4699771/ /pubmed/26727373 http://dx.doi.org/10.1371/journal.ppat.1005359 Text en © 2016 Connolly 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
Connolly, James P. R.
Gabrielsen, Mads
Goldstone, Robert J.
Grinter, Rhys
Wang, Dai
Cogdell, Richard J.
Walker, Daniel
Smith, David G. E.
Roe, Andrew J.
A Highly Conserved Bacterial D-Serine Uptake System Links Host Metabolism and Virulence
title A Highly Conserved Bacterial D-Serine Uptake System Links Host Metabolism and Virulence
title_full A Highly Conserved Bacterial D-Serine Uptake System Links Host Metabolism and Virulence
title_fullStr A Highly Conserved Bacterial D-Serine Uptake System Links Host Metabolism and Virulence
title_full_unstemmed A Highly Conserved Bacterial D-Serine Uptake System Links Host Metabolism and Virulence
title_short A Highly Conserved Bacterial D-Serine Uptake System Links Host Metabolism and Virulence
title_sort highly conserved bacterial d-serine uptake system links host metabolism and virulence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4699771/
https://www.ncbi.nlm.nih.gov/pubmed/26727373
http://dx.doi.org/10.1371/journal.ppat.1005359
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