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Flagellin-independent effects of a Toll-like receptor 5 polymorphism in the inflammatory response to Burkholderia pseudomallei

BACKGROUND: Toll-like receptors (TLRs) are sentinel receptors of the innate immune system. TLR4 detects bacterial lipopolysaccharide (LPS) and TLR5 detects bacterial flagellin. A common human nonsense polymorphism, TLR5:c.1174C>T, results in a non-functional TLR5 protein. Individuals carrying thi...

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Autores principales: Dickey, Amy K., Chantratita, Narisara, Tandhavanant, Sarunporn, Ducken, Deirdre, Lovelace-Macon, Lara, Seal, Sudeshna, Robertson, Johanna, Myers, Nicolle D., Schwarz, Sandra, Wurfel, Mark M., Kosamo, Susanna, West, T. Eoin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527242/
https://www.ncbi.nlm.nih.gov/pubmed/31067234
http://dx.doi.org/10.1371/journal.pntd.0007354
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author Dickey, Amy K.
Chantratita, Narisara
Tandhavanant, Sarunporn
Ducken, Deirdre
Lovelace-Macon, Lara
Seal, Sudeshna
Robertson, Johanna
Myers, Nicolle D.
Schwarz, Sandra
Wurfel, Mark M.
Kosamo, Susanna
West, T. Eoin
author_facet Dickey, Amy K.
Chantratita, Narisara
Tandhavanant, Sarunporn
Ducken, Deirdre
Lovelace-Macon, Lara
Seal, Sudeshna
Robertson, Johanna
Myers, Nicolle D.
Schwarz, Sandra
Wurfel, Mark M.
Kosamo, Susanna
West, T. Eoin
author_sort Dickey, Amy K.
collection PubMed
description BACKGROUND: Toll-like receptors (TLRs) are sentinel receptors of the innate immune system. TLR4 detects bacterial lipopolysaccharide (LPS) and TLR5 detects bacterial flagellin. A common human nonsense polymorphism, TLR5:c.1174C>T, results in a non-functional TLR5 protein. Individuals carrying this variant have decreased mortality from melioidosis, infection caused by the flagellated Gram-negative bacterium Burkholderia pseudomallei. Although impaired flagellin-dependent signaling in carriers of TLR5:c.1174C>T is well established, this study tested the hypothesis that a functional effect of TLR5:c.1174C>T is flagellin-independent and involves LPS-TLR4 pathways. METHODOLOGY/PRINCIPAL FINDINGS: Whole blood from two independent cohorts of individuals genotyped at TLR5:c.1174C>T was stimulated with wild type or aflagellated B. pseudomallei or purified bacterial motifs followed by plasma cytokine measurements. Blood from individuals carrying the TLR5:c.1174C>T variant produced less IL-6 and IL-10 in response to an aflagellated B. pseudomallei mutant and less IL-8 in response to purified B. pseudomallei LPS than blood from individuals without the variant. TLR5 expression in THP1 cells was silenced using siRNA; these cells were stimulated with LPS before cytokine levels in cell supernatants were quantified by ELISA. In these cells following LPS stimulation, silencing of TLR5 with siRNA reduced both TNF-α and IL-8 levels. These effects were not explained by differences in TLR4 mRNA expression or NF-κB or IRF activation. CONCLUSIONS/SIGNIFICANCE: The effects of the common nonsense TLR5:c.1174C>T polymorphism on the host inflammatory response to B. pseudomallei may not be restricted to flagellin-driven pathways. Moreover, TLR5 may modulate TLR4-dependent cytokine production. While these results may have broader implications for the role of TLR5 in the innate immune response in melioidosis and other conditions, further studies of the mechanisms underlying these observations are required.
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spelling pubmed-65272422019-05-31 Flagellin-independent effects of a Toll-like receptor 5 polymorphism in the inflammatory response to Burkholderia pseudomallei Dickey, Amy K. Chantratita, Narisara Tandhavanant, Sarunporn Ducken, Deirdre Lovelace-Macon, Lara Seal, Sudeshna Robertson, Johanna Myers, Nicolle D. Schwarz, Sandra Wurfel, Mark M. Kosamo, Susanna West, T. Eoin PLoS Negl Trop Dis Research Article BACKGROUND: Toll-like receptors (TLRs) are sentinel receptors of the innate immune system. TLR4 detects bacterial lipopolysaccharide (LPS) and TLR5 detects bacterial flagellin. A common human nonsense polymorphism, TLR5:c.1174C>T, results in a non-functional TLR5 protein. Individuals carrying this variant have decreased mortality from melioidosis, infection caused by the flagellated Gram-negative bacterium Burkholderia pseudomallei. Although impaired flagellin-dependent signaling in carriers of TLR5:c.1174C>T is well established, this study tested the hypothesis that a functional effect of TLR5:c.1174C>T is flagellin-independent and involves LPS-TLR4 pathways. METHODOLOGY/PRINCIPAL FINDINGS: Whole blood from two independent cohorts of individuals genotyped at TLR5:c.1174C>T was stimulated with wild type or aflagellated B. pseudomallei or purified bacterial motifs followed by plasma cytokine measurements. Blood from individuals carrying the TLR5:c.1174C>T variant produced less IL-6 and IL-10 in response to an aflagellated B. pseudomallei mutant and less IL-8 in response to purified B. pseudomallei LPS than blood from individuals without the variant. TLR5 expression in THP1 cells was silenced using siRNA; these cells were stimulated with LPS before cytokine levels in cell supernatants were quantified by ELISA. In these cells following LPS stimulation, silencing of TLR5 with siRNA reduced both TNF-α and IL-8 levels. These effects were not explained by differences in TLR4 mRNA expression or NF-κB or IRF activation. CONCLUSIONS/SIGNIFICANCE: The effects of the common nonsense TLR5:c.1174C>T polymorphism on the host inflammatory response to B. pseudomallei may not be restricted to flagellin-driven pathways. Moreover, TLR5 may modulate TLR4-dependent cytokine production. While these results may have broader implications for the role of TLR5 in the innate immune response in melioidosis and other conditions, further studies of the mechanisms underlying these observations are required. Public Library of Science 2019-05-08 /pmc/articles/PMC6527242/ /pubmed/31067234 http://dx.doi.org/10.1371/journal.pntd.0007354 Text en © 2019 Dickey 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dickey, Amy K.
Chantratita, Narisara
Tandhavanant, Sarunporn
Ducken, Deirdre
Lovelace-Macon, Lara
Seal, Sudeshna
Robertson, Johanna
Myers, Nicolle D.
Schwarz, Sandra
Wurfel, Mark M.
Kosamo, Susanna
West, T. Eoin
Flagellin-independent effects of a Toll-like receptor 5 polymorphism in the inflammatory response to Burkholderia pseudomallei
title Flagellin-independent effects of a Toll-like receptor 5 polymorphism in the inflammatory response to Burkholderia pseudomallei
title_full Flagellin-independent effects of a Toll-like receptor 5 polymorphism in the inflammatory response to Burkholderia pseudomallei
title_fullStr Flagellin-independent effects of a Toll-like receptor 5 polymorphism in the inflammatory response to Burkholderia pseudomallei
title_full_unstemmed Flagellin-independent effects of a Toll-like receptor 5 polymorphism in the inflammatory response to Burkholderia pseudomallei
title_short Flagellin-independent effects of a Toll-like receptor 5 polymorphism in the inflammatory response to Burkholderia pseudomallei
title_sort flagellin-independent effects of a toll-like receptor 5 polymorphism in the inflammatory response to burkholderia pseudomallei
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527242/
https://www.ncbi.nlm.nih.gov/pubmed/31067234
http://dx.doi.org/10.1371/journal.pntd.0007354
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