Influenza-induced immune suppression to methicillin-resistant Staphylococcus aureus is mediated by TLR9.

Bacterial lung infections, particularly with methicillin-resistant Staphylococcus aureus (MRSA), increase mortality following influenza infection, but the mechanisms remain unclear. Here we show that expression of TLR9, a microbial DNA sensor, is increased in murine lung macrophages, dendritic cells...

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Main Authors: Giovanny J Martínez-Colón, Helen Warheit-Niemi, Stephen J Gurczynski, Quincy M Taylor, Carol A Wilke, Amy B Podsiad, Joel Crespo, Urvashi Bhan, Bethany B Moore
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.1007560
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author Giovanny J Martínez-Colón
Helen Warheit-Niemi
Stephen J Gurczynski
Quincy M Taylor
Carol A Wilke
Amy B Podsiad
Joel Crespo
Urvashi Bhan
Bethany B Moore
author_facet Giovanny J Martínez-Colón
Helen Warheit-Niemi
Stephen J Gurczynski
Quincy M Taylor
Carol A Wilke
Amy B Podsiad
Joel Crespo
Urvashi Bhan
Bethany B Moore
author_sort Giovanny J Martínez-Colón
collection DOAJ
description Bacterial lung infections, particularly with methicillin-resistant Staphylococcus aureus (MRSA), increase mortality following influenza infection, but the mechanisms remain unclear. Here we show that expression of TLR9, a microbial DNA sensor, is increased in murine lung macrophages, dendritic cells, CD8+ T cells and epithelial cells post-influenza infection. TLR9-/- mice did not show differences in handling influenza nor MRSA infection alone. However, TLR9-/- mice have improved survival and bacterial clearance in the lung post-influenza and MRSA dual infection, with no difference in viral load during dual infection. We demonstrate that TLR9 is upregulated on macrophages even when they are not themselves infected, suggesting that TLR9 upregulation is related to soluble mediators. We rule out a role for elevations in interferon-γ (IFNγ) in mediating the beneficial MRSA clearance in TLR9-/- mice. While macrophages from WT and TLR9-/- mice show similar phagocytosis and bacterial killing to MRSA alone, following influenza infection, there is a marked upregulation of scavenger receptor A and MRSA phagocytosis as well as inducible nitric oxide synthase (Inos) and improved bacterial killing that is specific to TLR9-deficient cells. Bone marrow transplant chimera experiments and in vitro experiments using TLR9 antagonists suggest TLR9 expression on non-hematopoietic cells, rather than the macrophages themselves, is important for regulating myeloid cell function. Interestingly, improved bacterial clearance post-dual infection was restricted to MRSA, as there was no difference in the clearance of Streptococcus pneumoniae. Taken together these data show a surprising inhibitory role for TLR9 signaling in mediating clearance of MRSA that manifests following influenza infection.
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spelling doaj.art-51ceb92af3b2453281765c18d108805a2022-12-22T02:02:38ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742019-01-01151e100756010.1371/journal.ppat.1007560Influenza-induced immune suppression to methicillin-resistant Staphylococcus aureus is mediated by TLR9.Giovanny J Martínez-ColónHelen Warheit-NiemiStephen J GurczynskiQuincy M TaylorCarol A WilkeAmy B PodsiadJoel CrespoUrvashi BhanBethany B MooreBacterial lung infections, particularly with methicillin-resistant Staphylococcus aureus (MRSA), increase mortality following influenza infection, but the mechanisms remain unclear. Here we show that expression of TLR9, a microbial DNA sensor, is increased in murine lung macrophages, dendritic cells, CD8+ T cells and epithelial cells post-influenza infection. TLR9-/- mice did not show differences in handling influenza nor MRSA infection alone. However, TLR9-/- mice have improved survival and bacterial clearance in the lung post-influenza and MRSA dual infection, with no difference in viral load during dual infection. We demonstrate that TLR9 is upregulated on macrophages even when they are not themselves infected, suggesting that TLR9 upregulation is related to soluble mediators. We rule out a role for elevations in interferon-γ (IFNγ) in mediating the beneficial MRSA clearance in TLR9-/- mice. While macrophages from WT and TLR9-/- mice show similar phagocytosis and bacterial killing to MRSA alone, following influenza infection, there is a marked upregulation of scavenger receptor A and MRSA phagocytosis as well as inducible nitric oxide synthase (Inos) and improved bacterial killing that is specific to TLR9-deficient cells. Bone marrow transplant chimera experiments and in vitro experiments using TLR9 antagonists suggest TLR9 expression on non-hematopoietic cells, rather than the macrophages themselves, is important for regulating myeloid cell function. Interestingly, improved bacterial clearance post-dual infection was restricted to MRSA, as there was no difference in the clearance of Streptococcus pneumoniae. Taken together these data show a surprising inhibitory role for TLR9 signaling in mediating clearance of MRSA that manifests following influenza infection.https://doi.org/10.1371/journal.ppat.1007560
spellingShingle Giovanny J Martínez-Colón
Helen Warheit-Niemi
Stephen J Gurczynski
Quincy M Taylor
Carol A Wilke
Amy B Podsiad
Joel Crespo
Urvashi Bhan
Bethany B Moore
Influenza-induced immune suppression to methicillin-resistant Staphylococcus aureus is mediated by TLR9.
PLoS Pathogens
title Influenza-induced immune suppression to methicillin-resistant Staphylococcus aureus is mediated by TLR9.
title_full Influenza-induced immune suppression to methicillin-resistant Staphylococcus aureus is mediated by TLR9.
title_fullStr Influenza-induced immune suppression to methicillin-resistant Staphylococcus aureus is mediated by TLR9.
title_full_unstemmed Influenza-induced immune suppression to methicillin-resistant Staphylococcus aureus is mediated by TLR9.
title_short Influenza-induced immune suppression to methicillin-resistant Staphylococcus aureus is mediated by TLR9.
title_sort influenza induced immune suppression to methicillin resistant staphylococcus aureus is mediated by tlr9
url https://doi.org/10.1371/journal.ppat.1007560
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