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

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 ha...

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Veröffentlicht in:PLoS neglected tropical diseases 2019-05, Vol.13 (5), p.e0007354-e0007354
Hauptverfasser: 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
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container_issue 5
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container_title PLoS neglected tropical diseases
container_volume 13
creator 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
description 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. 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. 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.
doi_str_mv 10.1371/journal.pntd.0007354
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TLR4 detects bacterial lipopolysaccharide (LPS) and TLR5 detects bacterial flagellin. A common human nonsense polymorphism, TLR5:c.1174C&gt;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&gt;T is well established, this study tested the hypothesis that a functional effect of TLR5:c.1174C&gt;T is flagellin-independent and involves LPS-TLR4 pathways. Whole blood from two independent cohorts of individuals genotyped at TLR5:c.1174C&gt;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&gt;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. The effects of the common nonsense TLR5:c.1174C&gt;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.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0007354</identifier><identifier>PMID: 31067234</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adolescent ; Adult ; Aged ; Bacteria ; Biology and Life Sciences ; Blood ; Burkholderia pseudomallei ; Burkholderia pseudomallei - genetics ; Burkholderia pseudomallei - immunology ; Care and treatment ; Cells ; Cloning ; Codon, Nonsense ; Cohort Studies ; Cohorts ; Defence mechanisms ; ELISA ; Enzyme-linked immunosorbent assay ; Female ; Flagellin ; Flagellin - genetics ; Flagellin - immunology ; Gene expression ; Gene polymorphism ; Humans ; Immune response ; Immune system ; Immunity ; Immunity, Innate ; Immunology ; Infection ; Infections ; Infectious diseases ; Inflammation ; Inflammatory response ; Innate immunity ; Interleukin 10 ; Interleukin 6 ; Interleukin 8 ; Interleukin-10 - genetics ; Interleukin-10 - immunology ; Lipopolysaccharides ; Male ; Medicine ; Medicine and Health Sciences ; Melioidosis ; Melioidosis - genetics ; Melioidosis - immunology ; Melioidosis - microbiology ; Messenger RNA ; Middle Aged ; Mitogens ; Mortality ; NF-kappa B - genetics ; NF-kappa B - immunology ; NF-κB protein ; Point Mutation ; Polymorphism ; Polymorphism, Genetic ; Proteins ; Pseudomonas infections ; Receptors ; Risk factors ; RNA ; Sepsis ; siRNA ; TLR4 protein ; TLR5 ; TLR5 protein ; Toll-Like Receptor 5 - genetics ; Toll-Like Receptor 5 - immunology ; Toll-like receptors ; Tropical diseases ; Tumor Necrosis Factor-alpha - genetics ; Tumor Necrosis Factor-alpha - immunology ; Tumor necrosis factor-α ; Young Adult</subject><ispartof>PLoS neglected tropical diseases, 2019-05, Vol.13 (5), p.e0007354-e0007354</ispartof><rights>COPYRIGHT 2019 Public Library of Science</rights><rights>2019 Dickey et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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TLR4 detects bacterial lipopolysaccharide (LPS) and TLR5 detects bacterial flagellin. A common human nonsense polymorphism, TLR5:c.1174C&gt;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&gt;T is well established, this study tested the hypothesis that a functional effect of TLR5:c.1174C&gt;T is flagellin-independent and involves LPS-TLR4 pathways. Whole blood from two independent cohorts of individuals genotyped at TLR5:c.1174C&gt;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&gt;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. The effects of the common nonsense TLR5:c.1174C&gt;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.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Bacteria</subject><subject>Biology and Life Sciences</subject><subject>Blood</subject><subject>Burkholderia pseudomallei</subject><subject>Burkholderia pseudomallei - genetics</subject><subject>Burkholderia pseudomallei - immunology</subject><subject>Care and treatment</subject><subject>Cells</subject><subject>Cloning</subject><subject>Codon, Nonsense</subject><subject>Cohort Studies</subject><subject>Cohorts</subject><subject>Defence mechanisms</subject><subject>ELISA</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Female</subject><subject>Flagellin</subject><subject>Flagellin - genetics</subject><subject>Flagellin - immunology</subject><subject>Gene expression</subject><subject>Gene polymorphism</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immunity</subject><subject>Immunity, Innate</subject><subject>Immunology</subject><subject>Infection</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Inflammation</subject><subject>Inflammatory response</subject><subject>Innate immunity</subject><subject>Interleukin 10</subject><subject>Interleukin 6</subject><subject>Interleukin 8</subject><subject>Interleukin-10 - genetics</subject><subject>Interleukin-10 - immunology</subject><subject>Lipopolysaccharides</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine and Health Sciences</subject><subject>Melioidosis</subject><subject>Melioidosis - genetics</subject><subject>Melioidosis - immunology</subject><subject>Melioidosis - microbiology</subject><subject>Messenger RNA</subject><subject>Middle Aged</subject><subject>Mitogens</subject><subject>Mortality</subject><subject>NF-kappa B - genetics</subject><subject>NF-kappa B - immunology</subject><subject>NF-κB protein</subject><subject>Point Mutation</subject><subject>Polymorphism</subject><subject>Polymorphism, Genetic</subject><subject>Proteins</subject><subject>Pseudomonas infections</subject><subject>Receptors</subject><subject>Risk factors</subject><subject>RNA</subject><subject>Sepsis</subject><subject>siRNA</subject><subject>TLR4 protein</subject><subject>TLR5</subject><subject>TLR5 protein</subject><subject>Toll-Like Receptor 5 - genetics</subject><subject>Toll-Like Receptor 5 - immunology</subject><subject>Toll-like receptors</subject><subject>Tropical diseases</subject><subject>Tumor Necrosis Factor-alpha - genetics</subject><subject>Tumor Necrosis Factor-alpha - immunology</subject><subject>Tumor necrosis factor-α</subject><subject>Young Adult</subject><issn>1935-2735</issn><issn>1935-2727</issn><issn>1935-2735</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>DOA</sourceid><recordid>eNptkk1v1DAQhiMEoqXwDxBEQkJcsvgjTuILUqkoVKrEpZwtxx5vvHXiYCdIvfDbcbpptYsqS_585p3xzGTZW4w2mNb4887PYZBuMw6T3iCEasrKZ9kp5pQVJB2eH-xPslcx7hBinDX4ZXZCMapqQsvT7O-lk1twzg6FHTSMkKZhysEYUFPMvcllfuOdK5y9hTyAgnHyIWf56N1d78PY2djndsinDtJinOx7mYi7xMbRDxHyyedf53DbeachWJmPEWbte-kc2NfZCyNdhDfrepb9uvx2c_GjuP75_eri_LpQFSmngtEKM0JNgwFzRVtuKOJEt5ohUJpzrIiktTFEmraUTCNgbdNi1Zq2ooaW9Cx7v9cdnY9iTV0UhCRV3PB74mpPaC93Ygy2l-FOeGnF_YUPWyHDZJUDobhiBCPCSaVLaGpZa9VSzrDkFGQNSevL6m1ue9AqZTRIdyR6_DLYTmz9H1ExUpOSJIFPq0Dwv2eIk-htVKlMcgA_L3EvUTOGFvTDf-jTv1uprUwfSHXyya9aRMU5a-oakbJuErV5gkpDQ2-VH8DYdH9k8PHAoAPppi56N082Vf4YLPegCj7GAOYxGRiJpZ0fohZLO4u1nZPZu8NEPho99C_9B9RK9CI</recordid><startdate>20190501</startdate><enddate>20190501</enddate><creator>Dickey, Amy K</creator><creator>Chantratita, Narisara</creator><creator>Tandhavanant, Sarunporn</creator><creator>Ducken, Deirdre</creator><creator>Lovelace-Macon, Lara</creator><creator>Seal, Sudeshna</creator><creator>Robertson, Johanna</creator><creator>Myers, Nicolle D</creator><creator>Schwarz, Sandra</creator><creator>Wurfel, Mark M</creator><creator>Kosamo, Susanna</creator><creator>West, T Eoin</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7SS</scope><scope>7T2</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>K9.</scope><scope>L.G</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-4884-2835</orcidid><orcidid>https://orcid.org/0000-0003-2979-9664</orcidid><orcidid>https://orcid.org/0000-0001-5503-7204</orcidid></search><sort><creationdate>20190501</creationdate><title>Flagellin-independent effects of a Toll-like receptor 5 polymorphism in the inflammatory response to Burkholderia pseudomallei</title><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></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c624t-5361523f81e19c3b9f3092dbd50ecd991c2a37ff2afb4a5d0e5b8b1cbfb63f343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Bacteria</topic><topic>Biology and Life Sciences</topic><topic>Blood</topic><topic>Burkholderia pseudomallei</topic><topic>Burkholderia pseudomallei - genetics</topic><topic>Burkholderia pseudomallei - immunology</topic><topic>Care and treatment</topic><topic>Cells</topic><topic>Cloning</topic><topic>Codon, Nonsense</topic><topic>Cohort Studies</topic><topic>Cohorts</topic><topic>Defence mechanisms</topic><topic>ELISA</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Female</topic><topic>Flagellin</topic><topic>Flagellin - genetics</topic><topic>Flagellin - immunology</topic><topic>Gene expression</topic><topic>Gene polymorphism</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Immunity</topic><topic>Immunity, Innate</topic><topic>Immunology</topic><topic>Infection</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Inflammation</topic><topic>Inflammatory response</topic><topic>Innate immunity</topic><topic>Interleukin 10</topic><topic>Interleukin 6</topic><topic>Interleukin 8</topic><topic>Interleukin-10 - genetics</topic><topic>Interleukin-10 - immunology</topic><topic>Lipopolysaccharides</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine and Health Sciences</topic><topic>Melioidosis</topic><topic>Melioidosis - genetics</topic><topic>Melioidosis - immunology</topic><topic>Melioidosis - microbiology</topic><topic>Messenger RNA</topic><topic>Middle Aged</topic><topic>Mitogens</topic><topic>Mortality</topic><topic>NF-kappa B - genetics</topic><topic>NF-kappa B - immunology</topic><topic>NF-κB protein</topic><topic>Point Mutation</topic><topic>Polymorphism</topic><topic>Polymorphism, Genetic</topic><topic>Proteins</topic><topic>Pseudomonas infections</topic><topic>Receptors</topic><topic>Risk factors</topic><topic>RNA</topic><topic>Sepsis</topic><topic>siRNA</topic><topic>TLR4 protein</topic><topic>TLR5</topic><topic>TLR5 protein</topic><topic>Toll-Like Receptor 5 - genetics</topic><topic>Toll-Like Receptor 5 - immunology</topic><topic>Toll-like receptors</topic><topic>Tropical diseases</topic><topic>Tumor Necrosis Factor-alpha - genetics</topic><topic>Tumor Necrosis Factor-alpha - immunology</topic><topic>Tumor necrosis factor-α</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dickey, Amy K</creatorcontrib><creatorcontrib>Chantratita, Narisara</creatorcontrib><creatorcontrib>Tandhavanant, Sarunporn</creatorcontrib><creatorcontrib>Ducken, Deirdre</creatorcontrib><creatorcontrib>Lovelace-Macon, Lara</creatorcontrib><creatorcontrib>Seal, Sudeshna</creatorcontrib><creatorcontrib>Robertson, Johanna</creatorcontrib><creatorcontrib>Myers, Nicolle D</creatorcontrib><creatorcontrib>Schwarz, Sandra</creatorcontrib><creatorcontrib>Wurfel, Mark M</creatorcontrib><creatorcontrib>Kosamo, Susanna</creatorcontrib><creatorcontrib>West, T Eoin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) 1: Biological Sciences &amp; Living Resources</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) 3: Aquatic Pollution &amp; Environmental Quality</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) Professional</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS neglected tropical diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dickey, Amy K</au><au>Chantratita, Narisara</au><au>Tandhavanant, Sarunporn</au><au>Ducken, Deirdre</au><au>Lovelace-Macon, Lara</au><au>Seal, Sudeshna</au><au>Robertson, Johanna</au><au>Myers, Nicolle D</au><au>Schwarz, Sandra</au><au>Wurfel, Mark M</au><au>Kosamo, Susanna</au><au>West, T Eoin</au><au>Torres, Alfredo G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Flagellin-independent effects of a Toll-like receptor 5 polymorphism in the inflammatory response to Burkholderia pseudomallei</atitle><jtitle>PLoS neglected tropical diseases</jtitle><addtitle>PLoS Negl Trop Dis</addtitle><date>2019-05-01</date><risdate>2019</risdate><volume>13</volume><issue>5</issue><spage>e0007354</spage><epage>e0007354</epage><pages>e0007354-e0007354</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>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&gt;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&gt;T is well established, this study tested the hypothesis that a functional effect of TLR5:c.1174C&gt;T is flagellin-independent and involves LPS-TLR4 pathways. Whole blood from two independent cohorts of individuals genotyped at TLR5:c.1174C&gt;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&gt;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. The effects of the common nonsense TLR5:c.1174C&gt;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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>31067234</pmid><doi>10.1371/journal.pntd.0007354</doi><orcidid>https://orcid.org/0000-0002-4884-2835</orcidid><orcidid>https://orcid.org/0000-0003-2979-9664</orcidid><orcidid>https://orcid.org/0000-0001-5503-7204</orcidid><oa>free_for_read</oa></addata></record>
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1935-2735
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subjects Adolescent
Adult
Aged
Bacteria
Biology and Life Sciences
Blood
Burkholderia pseudomallei
Burkholderia pseudomallei - genetics
Burkholderia pseudomallei - immunology
Care and treatment
Cells
Cloning
Codon, Nonsense
Cohort Studies
Cohorts
Defence mechanisms
ELISA
Enzyme-linked immunosorbent assay
Female
Flagellin
Flagellin - genetics
Flagellin - immunology
Gene expression
Gene polymorphism
Humans
Immune response
Immune system
Immunity
Immunity, Innate
Immunology
Infection
Infections
Infectious diseases
Inflammation
Inflammatory response
Innate immunity
Interleukin 10
Interleukin 6
Interleukin 8
Interleukin-10 - genetics
Interleukin-10 - immunology
Lipopolysaccharides
Male
Medicine
Medicine and Health Sciences
Melioidosis
Melioidosis - genetics
Melioidosis - immunology
Melioidosis - microbiology
Messenger RNA
Middle Aged
Mitogens
Mortality
NF-kappa B - genetics
NF-kappa B - immunology
NF-κB protein
Point Mutation
Polymorphism
Polymorphism, Genetic
Proteins
Pseudomonas infections
Receptors
Risk factors
RNA
Sepsis
siRNA
TLR4 protein
TLR5
TLR5 protein
Toll-Like Receptor 5 - genetics
Toll-Like Receptor 5 - immunology
Toll-like receptors
Tropical diseases
Tumor Necrosis Factor-alpha - genetics
Tumor Necrosis Factor-alpha - immunology
Tumor necrosis factor-α
Young Adult
title Flagellin-independent effects of a Toll-like receptor 5 polymorphism in the inflammatory response to Burkholderia pseudomallei
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