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Evolution of Salmonella-Host Cell Interactions through a Dynamic Bacterial Genome

Salmonella Typhimurium has a broad arsenal of genes that are tightly regulated and coordinated to facilitate adaptation to the various host environments it colonizes. The genome of Salmonella Typhimurium has undergone multiple gene acquisition events and has accrued changes in non-coding DNA that ha...

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Autores principales: Ilyas, Bushra, Tsai, Caressa N., Coombes, Brian K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626846/
https://www.ncbi.nlm.nih.gov/pubmed/29034217
http://dx.doi.org/10.3389/fcimb.2017.00428
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author Ilyas, Bushra
Tsai, Caressa N.
Coombes, Brian K.
author_facet Ilyas, Bushra
Tsai, Caressa N.
Coombes, Brian K.
author_sort Ilyas, Bushra
collection PubMed
description Salmonella Typhimurium has a broad arsenal of genes that are tightly regulated and coordinated to facilitate adaptation to the various host environments it colonizes. The genome of Salmonella Typhimurium has undergone multiple gene acquisition events and has accrued changes in non-coding DNA that have undergone selection by regulatory evolution. Together, at least 17 horizontally acquired pathogenicity islands (SPIs), prophage-associated genes, and changes in core genome regulation contribute to the virulence program of Salmonella. Here, we review the latest understanding of these elements and their contributions to pathogenesis, emphasizing the regulatory circuitry that controls niche-specific gene expression. In addition to an overview of the importance of SPI-1 and SPI-2 to host invasion and colonization, we describe the recently characterized contributions of other SPIs, including the antibacterial activity of SPI-6 and adhesion and invasion mediated by SPI-4. We further discuss how these fitness traits have been integrated into the regulatory circuitry of the bacterial cell through cis-regulatory evolution and by a careful balance of silencing and counter-silencing by regulatory proteins. Detailed understanding of regulatory evolution within Salmonella is uncovering novel aspects of infection biology that relate to host-pathogen interactions and evasion of host immunity.
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spelling pubmed-56268462017-10-13 Evolution of Salmonella-Host Cell Interactions through a Dynamic Bacterial Genome Ilyas, Bushra Tsai, Caressa N. Coombes, Brian K. Front Cell Infect Microbiol Microbiology Salmonella Typhimurium has a broad arsenal of genes that are tightly regulated and coordinated to facilitate adaptation to the various host environments it colonizes. The genome of Salmonella Typhimurium has undergone multiple gene acquisition events and has accrued changes in non-coding DNA that have undergone selection by regulatory evolution. Together, at least 17 horizontally acquired pathogenicity islands (SPIs), prophage-associated genes, and changes in core genome regulation contribute to the virulence program of Salmonella. Here, we review the latest understanding of these elements and their contributions to pathogenesis, emphasizing the regulatory circuitry that controls niche-specific gene expression. In addition to an overview of the importance of SPI-1 and SPI-2 to host invasion and colonization, we describe the recently characterized contributions of other SPIs, including the antibacterial activity of SPI-6 and adhesion and invasion mediated by SPI-4. We further discuss how these fitness traits have been integrated into the regulatory circuitry of the bacterial cell through cis-regulatory evolution and by a careful balance of silencing and counter-silencing by regulatory proteins. Detailed understanding of regulatory evolution within Salmonella is uncovering novel aspects of infection biology that relate to host-pathogen interactions and evasion of host immunity. Frontiers Media S.A. 2017-09-29 /pmc/articles/PMC5626846/ /pubmed/29034217 http://dx.doi.org/10.3389/fcimb.2017.00428 Text en Copyright © 2017 Ilyas, Tsai and Coombes. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Ilyas, Bushra
Tsai, Caressa N.
Coombes, Brian K.
Evolution of Salmonella-Host Cell Interactions through a Dynamic Bacterial Genome
title Evolution of Salmonella-Host Cell Interactions through a Dynamic Bacterial Genome
title_full Evolution of Salmonella-Host Cell Interactions through a Dynamic Bacterial Genome
title_fullStr Evolution of Salmonella-Host Cell Interactions through a Dynamic Bacterial Genome
title_full_unstemmed Evolution of Salmonella-Host Cell Interactions through a Dynamic Bacterial Genome
title_short Evolution of Salmonella-Host Cell Interactions through a Dynamic Bacterial Genome
title_sort evolution of salmonella-host cell interactions through a dynamic bacterial genome
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626846/
https://www.ncbi.nlm.nih.gov/pubmed/29034217
http://dx.doi.org/10.3389/fcimb.2017.00428
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