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Host species adaptation of TLR5 signalling and flagellin recognition
Toll-like receptor 5 (TLR5) recognition of flagellin instigates inflammatory signalling. Significant sequence variation in TLR5 exists between animal species but its impact on activity is less well understood. Building on our previous research that bovine TLR5 (bTLR5) is functional, we compared huma...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732158/ https://www.ncbi.nlm.nih.gov/pubmed/29247203 http://dx.doi.org/10.1038/s41598-017-17935-5 |
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author | Tahoun, Amin Jensen, Kirsty Corripio-Miyar, Yolanda McAteer, Sean Smith, David G. E. McNeilly, Tom N. Gally, David L. Glass, Elizabeth J. |
author_facet | Tahoun, Amin Jensen, Kirsty Corripio-Miyar, Yolanda McAteer, Sean Smith, David G. E. McNeilly, Tom N. Gally, David L. Glass, Elizabeth J. |
author_sort | Tahoun, Amin |
collection | PubMed |
description | Toll-like receptor 5 (TLR5) recognition of flagellin instigates inflammatory signalling. Significant sequence variation in TLR5 exists between animal species but its impact on activity is less well understood. Building on our previous research that bovine TLR5 (bTLR5) is functional, we compared human and bovine TLR5 activity and signalling in cognate cell lines. bTLR5 induced higher levels of CXCL8 when expressed in bovine cells and reciprocal results were found for human TLR5 (hTLR5) in human cells, indicative of host cell specificity in this response. Analysis of Toll/interleukin-1 receptor (TIR) sequences indicated that these differential responses involve cognate MyD88 recognition. siRNA knockdowns and inhibitor experiments demonstrated that there are some host differences in signalling. Although, PI3K activation is required for bTLR5 signalling, mutating bTLR5 F798 to hTLR5 Y798 within a putative PI3K motif resulted in a significantly reduced response. All ruminants have F798 in contrast to most other species, suggesting that TLR5 signalling has evolved differently in ruminants. Evolutionary divergence between bovine and human TLR5 was also apparent in relation to responses measured to diverse bacterial flagellins. Our results underscore the importance of species specific studies and how differences may alter efficacy of TLR-based vaccine adjuvants. |
format | Online Article Text |
id | pubmed-5732158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57321582017-12-21 Host species adaptation of TLR5 signalling and flagellin recognition Tahoun, Amin Jensen, Kirsty Corripio-Miyar, Yolanda McAteer, Sean Smith, David G. E. McNeilly, Tom N. Gally, David L. Glass, Elizabeth J. Sci Rep Article Toll-like receptor 5 (TLR5) recognition of flagellin instigates inflammatory signalling. Significant sequence variation in TLR5 exists between animal species but its impact on activity is less well understood. Building on our previous research that bovine TLR5 (bTLR5) is functional, we compared human and bovine TLR5 activity and signalling in cognate cell lines. bTLR5 induced higher levels of CXCL8 when expressed in bovine cells and reciprocal results were found for human TLR5 (hTLR5) in human cells, indicative of host cell specificity in this response. Analysis of Toll/interleukin-1 receptor (TIR) sequences indicated that these differential responses involve cognate MyD88 recognition. siRNA knockdowns and inhibitor experiments demonstrated that there are some host differences in signalling. Although, PI3K activation is required for bTLR5 signalling, mutating bTLR5 F798 to hTLR5 Y798 within a putative PI3K motif resulted in a significantly reduced response. All ruminants have F798 in contrast to most other species, suggesting that TLR5 signalling has evolved differently in ruminants. Evolutionary divergence between bovine and human TLR5 was also apparent in relation to responses measured to diverse bacterial flagellins. Our results underscore the importance of species specific studies and how differences may alter efficacy of TLR-based vaccine adjuvants. Nature Publishing Group UK 2017-12-15 /pmc/articles/PMC5732158/ /pubmed/29247203 http://dx.doi.org/10.1038/s41598-017-17935-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tahoun, Amin Jensen, Kirsty Corripio-Miyar, Yolanda McAteer, Sean Smith, David G. E. McNeilly, Tom N. Gally, David L. Glass, Elizabeth J. Host species adaptation of TLR5 signalling and flagellin recognition |
title | Host species adaptation of TLR5 signalling and flagellin recognition |
title_full | Host species adaptation of TLR5 signalling and flagellin recognition |
title_fullStr | Host species adaptation of TLR5 signalling and flagellin recognition |
title_full_unstemmed | Host species adaptation of TLR5 signalling and flagellin recognition |
title_short | Host species adaptation of TLR5 signalling and flagellin recognition |
title_sort | host species adaptation of tlr5 signalling and flagellin recognition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732158/ https://www.ncbi.nlm.nih.gov/pubmed/29247203 http://dx.doi.org/10.1038/s41598-017-17935-5 |
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