Location, location, location. Salmonella senses ethanolamine to gauge distinct host environments and coordinate gene expression

Authors:

Christopher J. Anderson and Melissa M. Kendall

doi: 10.15698/mic2016.02.479
Volume 3, pp. 89 to 91, published 18/01/2016.

Affiliations:

Department of Microbiology, Immunology, and Cancer Biology, University of Virginia School of Medicine, Charlottesville, Virginia, U.S.A.

Keywords: 

Salmonella, ethanolamine, macrophages, GI tract, metabolism.

Corresponding Author(s):

Melissa M. Kendall, melissakendall@virginia.edu

Conflict of interest statement:

The authors declare that no competing interest exists.

Please cite this article as:

Christopher J. Anderson and Melissa M. Kendall (2016). Location, location, location. Salmonella senses ethanolamine to gauge distinct host environments and coordinate gene expression. Microbial Cell 3(2): 89-91. doi: 10.15698/mic2016.02.479

© 2016 Anderson and Kendall. This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged.

Abstract:

Chemical and nutrient signaling mediate all cellular processes, ensuring survival in response to changing environmental conditions. Ethanolamine is a component of phosphatidylethanolamine, a major phospholipid of mammalian and bacterial cell membranes. Ethanolamine is abundant in the gastrointestinal (GI) tract from dietary sources as well as from the normal turnover of intestinal epithelial and bacterial cells in the gut. Additionally, mammalian cells maintain intracellular ethanolamine concentrations through low and high-affinity uptake systems and the internal recycling of phosphatidylethanolamine; therefore, ethanolamine is ubiquitous throughout the mammalian host. Although ethanolamine has profound signaling activity within mammalian cells by modulating inflammatory responses and intestinal physiology, ethanolamine is best appreciated as a nutrient for bacteria that supports growth. In our recent work (Anderson, et al. PLoS Pathog (2015), 11: e1005278), we demonstrated that Salmonella enterica serovar Typhimurium (Salmonella) exploits ethanolamine signaling to adapt to distinct host environments to precisely coordinate expression of genes encoding metabolism and virulence, which ultimately enhances disease progression.