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Purinergic Signaling: A Common Path in the Macrophage Response against Mycobacterium tuberculosis and Toxoplasma gondii

Authors :
Laetitia Petit-Jentreau
Ludovic Tailleux
Janine L. Coombes
University of Liverpool
Pathogénomique mycobactérienne intégrée
Institut Pasteur [Paris] (IP)
Génétique mycobactérienne - Mycobacterial genetics
The present work was supported by the University of Liverpool. JLC is a lecturer at the University of Liverpool, UK
LT is a researcher at Institut Pasteur, France
and LP-J is a postdoctoral researcher on the JLC's Biotechnology and Biological Sciences Research Council (BBSRC) grant (BB/M023540/1) at the University of Liverpool, UK.
LP-J wrote the paper with input from LT and JLC. All authors revised the manuscript, and approved it for publication.
Institut Pasteur [Paris]
Source :
Frontiers in Cellular and Infection Microbiology, Frontiers in Cellular and Infection Microbiology, 2017, 7, pp.347. ⟨10.3389/fcimb.2017.00347⟩, Frontiers in Cellular and Infection Microbiology, Vol 7 (2017), Frontiers in Cellular and Infection Microbiology, Frontiers, 2017, 7, pp.347. ⟨10.3389/fcimb.2017.00347⟩
Publication Year :
2017
Publisher :
Frontiers Media S.A., 2017.

Abstract

International audience; Immune responses are essential for the protection of the host against external dangers or infections and are normally efficient in the clearance of invading microbes. However, some intracellular pathogens have developed strategies to replicate and survive within host cells resulting in latent infection associated with strong inflammation. This excessive response can cause cell and tissue damage and lead to the release of the intracellular content, in particular the nucleotide pool, into the extracellular space. Over the last decade, new studies have implicated metabolites from the purinergic pathway in shaping the host immune response against intracellular pathogens and proved their importance in the outcome of the infection. This review aims to summarize how the immune system employs the purinergic system either to fight the pathogen, or to control collateral tissue damage. This will be achieved by focusing on the macrophage response against two intracellular pathogens, the human etiologic agent of tuberculosis, Mycobacterium tuberculosis and the protozoan parasite, Toxoplasma gondii.

Details

Language :
English
ISSN :
22352988
Volume :
7
Database :
OpenAIRE
Journal :
Frontiers in Cellular and Infection Microbiology
Accession number :
edsair.doi.dedup.....757cb985c381d546afa00e2d0de56920
Full Text :
https://doi.org/10.3389/fcimb.2017.00347