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Outrunning the Red Queen: bystander activation as a means of outpacing innate immune subversion by intracellular pathogens

Originally described by the late evolutionary biologist Leigh Van Valen, the Red Queen hypothesis posits that the evolutionary arms race between hosts and their pathogens selects for discrete, genetically encoded events that lead to competitive advantages over the other species. Examples of immune e...

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Autores principales: Holmgren, Alicia M, McConkey, Cameron A, Shin, Sunny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214943/
https://www.ncbi.nlm.nih.gov/pubmed/27545071
http://dx.doi.org/10.1038/cmi.2016.36
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author Holmgren, Alicia M
McConkey, Cameron A
Shin, Sunny
author_facet Holmgren, Alicia M
McConkey, Cameron A
Shin, Sunny
author_sort Holmgren, Alicia M
collection PubMed
description Originally described by the late evolutionary biologist Leigh Van Valen, the Red Queen hypothesis posits that the evolutionary arms race between hosts and their pathogens selects for discrete, genetically encoded events that lead to competitive advantages over the other species. Examples of immune evasion strategies are seen throughout the co-evolution of the mammalian immune system and pathogens, such as the enzymatic inactivation of nuclear factor-κB signaling or host translation by pathogen-encoded virulence factors. Such immunoevasive maneuvers would be expected to select for the evolution of innate immune counterstrategies. Recent advances in our understanding of host immunity and microbial pathogenesis have provided insight into a particular innate immune adaptation, termed bystander activation. Bystander activation occurs as a consequence of infected cells alerting and instructing neighboring uninfected cells to produce inflammatory mediators, either through direct cell contact or paracrine signals. Thus, bystander activation can allow the immune system to overcome the ability of pathogens to disarm immune signaling in directly infected cells. This review presents an overview of the general hallmarks of bystander activation and their emerging role in innate immunity to intracellular pathogens, as well as examples of recent mechanistic discoveries relating to the bystander activation during infection with specific pathogens relevant to human health and disease.
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spelling pubmed-52149432017-01-13 Outrunning the Red Queen: bystander activation as a means of outpacing innate immune subversion by intracellular pathogens Holmgren, Alicia M McConkey, Cameron A Shin, Sunny Cell Mol Immunol Review Originally described by the late evolutionary biologist Leigh Van Valen, the Red Queen hypothesis posits that the evolutionary arms race between hosts and their pathogens selects for discrete, genetically encoded events that lead to competitive advantages over the other species. Examples of immune evasion strategies are seen throughout the co-evolution of the mammalian immune system and pathogens, such as the enzymatic inactivation of nuclear factor-κB signaling or host translation by pathogen-encoded virulence factors. Such immunoevasive maneuvers would be expected to select for the evolution of innate immune counterstrategies. Recent advances in our understanding of host immunity and microbial pathogenesis have provided insight into a particular innate immune adaptation, termed bystander activation. Bystander activation occurs as a consequence of infected cells alerting and instructing neighboring uninfected cells to produce inflammatory mediators, either through direct cell contact or paracrine signals. Thus, bystander activation can allow the immune system to overcome the ability of pathogens to disarm immune signaling in directly infected cells. This review presents an overview of the general hallmarks of bystander activation and their emerging role in innate immunity to intracellular pathogens, as well as examples of recent mechanistic discoveries relating to the bystander activation during infection with specific pathogens relevant to human health and disease. Nature Publishing Group 2017-01 2016-08-22 /pmc/articles/PMC5214943/ /pubmed/27545071 http://dx.doi.org/10.1038/cmi.2016.36 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Review
Holmgren, Alicia M
McConkey, Cameron A
Shin, Sunny
Outrunning the Red Queen: bystander activation as a means of outpacing innate immune subversion by intracellular pathogens
title Outrunning the Red Queen: bystander activation as a means of outpacing innate immune subversion by intracellular pathogens
title_full Outrunning the Red Queen: bystander activation as a means of outpacing innate immune subversion by intracellular pathogens
title_fullStr Outrunning the Red Queen: bystander activation as a means of outpacing innate immune subversion by intracellular pathogens
title_full_unstemmed Outrunning the Red Queen: bystander activation as a means of outpacing innate immune subversion by intracellular pathogens
title_short Outrunning the Red Queen: bystander activation as a means of outpacing innate immune subversion by intracellular pathogens
title_sort outrunning the red queen: bystander activation as a means of outpacing innate immune subversion by intracellular pathogens
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214943/
https://www.ncbi.nlm.nih.gov/pubmed/27545071
http://dx.doi.org/10.1038/cmi.2016.36
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