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Potentiation of P2RX7 as a host-directed strategy for control of mycobacterial infection

Mycobacterium tuberculosis is the leading worldwide cause of death due to a single infectious agent. Existing anti-tuberculous therapies require long treatments and are complicated by multi-drug-resistant strains. Host-directed therapies have been proposed as an orthogonal approach, but few have mov...

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Autores principales: Matty, Molly A, Knudsen, Daphne R, Walton, Eric M, Beerman, Rebecca W, Cronan, Mark R, Pyle, Charlie J, Hernandez, Rafael E, Tobin, David M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351102/
https://www.ncbi.nlm.nih.gov/pubmed/30693866
http://dx.doi.org/10.7554/eLife.39123
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author Matty, Molly A
Knudsen, Daphne R
Walton, Eric M
Beerman, Rebecca W
Cronan, Mark R
Pyle, Charlie J
Hernandez, Rafael E
Tobin, David M
author_facet Matty, Molly A
Knudsen, Daphne R
Walton, Eric M
Beerman, Rebecca W
Cronan, Mark R
Pyle, Charlie J
Hernandez, Rafael E
Tobin, David M
author_sort Matty, Molly A
collection PubMed
description Mycobacterium tuberculosis is the leading worldwide cause of death due to a single infectious agent. Existing anti-tuberculous therapies require long treatments and are complicated by multi-drug-resistant strains. Host-directed therapies have been proposed as an orthogonal approach, but few have moved into clinical trials. Here, we use the zebrafish-Mycobacterium marinum infection model as a whole-animal screening platform to identify FDA-approved, host-directed compounds. We identify multiple compounds that modulate host immunity to limit mycobacterial disease, including the inexpensive, safe, and widely used drug clemastine. We find that clemastine alters macrophage calcium transients through potentiation of the purinergic receptor P2RX7. Host-directed drug activity in zebrafish larvae depends on both P2RX7 and inflammasome signaling. Thus, targeted activation of a P2RX7 axis provides a novel strategy for enhanced control of mycobacterial infections. Using a novel explant model, we find that clemastine is also effective within the complex granulomas that are the hallmark of mycobacterial infection.
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spelling pubmed-63511022019-01-30 Potentiation of P2RX7 as a host-directed strategy for control of mycobacterial infection Matty, Molly A Knudsen, Daphne R Walton, Eric M Beerman, Rebecca W Cronan, Mark R Pyle, Charlie J Hernandez, Rafael E Tobin, David M eLife Immunology and Inflammation Mycobacterium tuberculosis is the leading worldwide cause of death due to a single infectious agent. Existing anti-tuberculous therapies require long treatments and are complicated by multi-drug-resistant strains. Host-directed therapies have been proposed as an orthogonal approach, but few have moved into clinical trials. Here, we use the zebrafish-Mycobacterium marinum infection model as a whole-animal screening platform to identify FDA-approved, host-directed compounds. We identify multiple compounds that modulate host immunity to limit mycobacterial disease, including the inexpensive, safe, and widely used drug clemastine. We find that clemastine alters macrophage calcium transients through potentiation of the purinergic receptor P2RX7. Host-directed drug activity in zebrafish larvae depends on both P2RX7 and inflammasome signaling. Thus, targeted activation of a P2RX7 axis provides a novel strategy for enhanced control of mycobacterial infections. Using a novel explant model, we find that clemastine is also effective within the complex granulomas that are the hallmark of mycobacterial infection. eLife Sciences Publications, Ltd 2019-01-29 /pmc/articles/PMC6351102/ /pubmed/30693866 http://dx.doi.org/10.7554/eLife.39123 Text en © 2019, Matty et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Immunology and Inflammation
Matty, Molly A
Knudsen, Daphne R
Walton, Eric M
Beerman, Rebecca W
Cronan, Mark R
Pyle, Charlie J
Hernandez, Rafael E
Tobin, David M
Potentiation of P2RX7 as a host-directed strategy for control of mycobacterial infection
title Potentiation of P2RX7 as a host-directed strategy for control of mycobacterial infection
title_full Potentiation of P2RX7 as a host-directed strategy for control of mycobacterial infection
title_fullStr Potentiation of P2RX7 as a host-directed strategy for control of mycobacterial infection
title_full_unstemmed Potentiation of P2RX7 as a host-directed strategy for control of mycobacterial infection
title_short Potentiation of P2RX7 as a host-directed strategy for control of mycobacterial infection
title_sort potentiation of p2rx7 as a host-directed strategy for control of mycobacterial infection
topic Immunology and Inflammation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351102/
https://www.ncbi.nlm.nih.gov/pubmed/30693866
http://dx.doi.org/10.7554/eLife.39123
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