Cargando…

The Pore-Forming Toxin β hemolysin/cytolysin Triggers p38 MAPK-Dependent IL-10 Production in Macrophages and Inhibits Innate Immunity

Group B Streptococcus (GBS) is a leading cause of invasive bacterial infections in human newborns and immune-compromised adults. The pore-forming toxin (PFT) β hemolysin/cytolysin (βh/c) is a major virulence factor for GBS, which is generally attributed to its cytolytic functions. Here we show βh/c...

Descripción completa

Detalles Bibliográficos
Autores principales: Bebien, Magali, Hensler, Mary E., Davanture, Suzel, Hsu, Li-Chung, Karin, Michael, Park, Jin Mo, Alexopoulou, Lena, Liu, George Y., Nizet, Victor, Lawrence, Toby
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400567/
https://www.ncbi.nlm.nih.gov/pubmed/22829768
http://dx.doi.org/10.1371/journal.ppat.1002812
_version_ 1782238501238996992
author Bebien, Magali
Hensler, Mary E.
Davanture, Suzel
Hsu, Li-Chung
Karin, Michael
Park, Jin Mo
Alexopoulou, Lena
Liu, George Y.
Nizet, Victor
Lawrence, Toby
author_facet Bebien, Magali
Hensler, Mary E.
Davanture, Suzel
Hsu, Li-Chung
Karin, Michael
Park, Jin Mo
Alexopoulou, Lena
Liu, George Y.
Nizet, Victor
Lawrence, Toby
author_sort Bebien, Magali
collection PubMed
description Group B Streptococcus (GBS) is a leading cause of invasive bacterial infections in human newborns and immune-compromised adults. The pore-forming toxin (PFT) β hemolysin/cytolysin (βh/c) is a major virulence factor for GBS, which is generally attributed to its cytolytic functions. Here we show βh/c has immunomodulatory properties on macrophages at sub-lytic concentrations. βh/c-mediated activation of p38 MAPK drives expression of the anti-inflammatory and immunosuppressive cytokine IL-10, and inhibits both IL-12 and NOS2 expression in GBS-infected macrophages, which are critical factors in host defense. Isogenic mutant bacteria lacking βh/c fail to activate p38-mediated IL-10 production in macrophages and promote increased IL-12 and NOS2 expression. Furthermore, targeted deletion of p38 in macrophages increases resistance to invasive GBS infection in mice, associated with impaired IL-10 induction and increased IL-12 production in vivo. These data suggest p38 MAPK activation by βh/c contributes to evasion of host defense through induction of IL-10 expression and inhibition of macrophage activation, a new mechanism of action for a PFT and a novel anti-inflammatory role for p38 in the pathogenesis of invasive bacterial infection. Our studies suggest p38 MAPK may represent a new therapeutic target to blunt virulence and improve clinical outcome of invasive GBS infection.
format Online
Article
Text
id pubmed-3400567
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-34005672012-07-24 The Pore-Forming Toxin β hemolysin/cytolysin Triggers p38 MAPK-Dependent IL-10 Production in Macrophages and Inhibits Innate Immunity Bebien, Magali Hensler, Mary E. Davanture, Suzel Hsu, Li-Chung Karin, Michael Park, Jin Mo Alexopoulou, Lena Liu, George Y. Nizet, Victor Lawrence, Toby PLoS Pathog Research Article Group B Streptococcus (GBS) is a leading cause of invasive bacterial infections in human newborns and immune-compromised adults. The pore-forming toxin (PFT) β hemolysin/cytolysin (βh/c) is a major virulence factor for GBS, which is generally attributed to its cytolytic functions. Here we show βh/c has immunomodulatory properties on macrophages at sub-lytic concentrations. βh/c-mediated activation of p38 MAPK drives expression of the anti-inflammatory and immunosuppressive cytokine IL-10, and inhibits both IL-12 and NOS2 expression in GBS-infected macrophages, which are critical factors in host defense. Isogenic mutant bacteria lacking βh/c fail to activate p38-mediated IL-10 production in macrophages and promote increased IL-12 and NOS2 expression. Furthermore, targeted deletion of p38 in macrophages increases resistance to invasive GBS infection in mice, associated with impaired IL-10 induction and increased IL-12 production in vivo. These data suggest p38 MAPK activation by βh/c contributes to evasion of host defense through induction of IL-10 expression and inhibition of macrophage activation, a new mechanism of action for a PFT and a novel anti-inflammatory role for p38 in the pathogenesis of invasive bacterial infection. Our studies suggest p38 MAPK may represent a new therapeutic target to blunt virulence and improve clinical outcome of invasive GBS infection. Public Library of Science 2012-07-19 /pmc/articles/PMC3400567/ /pubmed/22829768 http://dx.doi.org/10.1371/journal.ppat.1002812 Text en Bebien et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bebien, Magali
Hensler, Mary E.
Davanture, Suzel
Hsu, Li-Chung
Karin, Michael
Park, Jin Mo
Alexopoulou, Lena
Liu, George Y.
Nizet, Victor
Lawrence, Toby
The Pore-Forming Toxin β hemolysin/cytolysin Triggers p38 MAPK-Dependent IL-10 Production in Macrophages and Inhibits Innate Immunity
title The Pore-Forming Toxin β hemolysin/cytolysin Triggers p38 MAPK-Dependent IL-10 Production in Macrophages and Inhibits Innate Immunity
title_full The Pore-Forming Toxin β hemolysin/cytolysin Triggers p38 MAPK-Dependent IL-10 Production in Macrophages and Inhibits Innate Immunity
title_fullStr The Pore-Forming Toxin β hemolysin/cytolysin Triggers p38 MAPK-Dependent IL-10 Production in Macrophages and Inhibits Innate Immunity
title_full_unstemmed The Pore-Forming Toxin β hemolysin/cytolysin Triggers p38 MAPK-Dependent IL-10 Production in Macrophages and Inhibits Innate Immunity
title_short The Pore-Forming Toxin β hemolysin/cytolysin Triggers p38 MAPK-Dependent IL-10 Production in Macrophages and Inhibits Innate Immunity
title_sort pore-forming toxin β hemolysin/cytolysin triggers p38 mapk-dependent il-10 production in macrophages and inhibits innate immunity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400567/
https://www.ncbi.nlm.nih.gov/pubmed/22829768
http://dx.doi.org/10.1371/journal.ppat.1002812
work_keys_str_mv AT bebienmagali theporeformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT henslermarye theporeformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT davanturesuzel theporeformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT hsulichung theporeformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT karinmichael theporeformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT parkjinmo theporeformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT alexopouloulena theporeformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT liugeorgey theporeformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT nizetvictor theporeformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT lawrencetoby theporeformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT bebienmagali poreformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT henslermarye poreformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT davanturesuzel poreformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT hsulichung poreformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT karinmichael poreformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT parkjinmo poreformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT alexopouloulena poreformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT liugeorgey poreformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT nizetvictor poreformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity
AT lawrencetoby poreformingtoxinbhemolysincytolysintriggersp38mapkdependentil10productioninmacrophagesandinhibitsinnateimmunity