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Reptile Toll-like receptor 5 unveils adaptive evolution of bacterial flagellin recognition

Toll-like receptors (TLR) are ancient innate immune receptors crucial for immune homeostasis and protection against infection. TLRs are present in mammals, birds, amphibians and fish but have not been functionally characterized in reptiles despite the central position of this animal class in vertebr...

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Autores principales: Voogdt, Carlos G. P., Bouwman, Lieneke I., Kik, Marja J. L., Wagenaar, Jaap A., van Putten, Jos P. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4703953/
https://www.ncbi.nlm.nih.gov/pubmed/26738735
http://dx.doi.org/10.1038/srep19046
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author Voogdt, Carlos G. P.
Bouwman, Lieneke I.
Kik, Marja J. L.
Wagenaar, Jaap A.
van Putten, Jos P. M.
author_facet Voogdt, Carlos G. P.
Bouwman, Lieneke I.
Kik, Marja J. L.
Wagenaar, Jaap A.
van Putten, Jos P. M.
author_sort Voogdt, Carlos G. P.
collection PubMed
description Toll-like receptors (TLR) are ancient innate immune receptors crucial for immune homeostasis and protection against infection. TLRs are present in mammals, birds, amphibians and fish but have not been functionally characterized in reptiles despite the central position of this animal class in vertebrate evolution. Here we report the cloning, characterization, and function of TLR5 of the reptile Anolis carolinensis (Green Anole lizard). The receptor (acTLR5) displays the typical TLR protein architecture with 22 extracellular leucine rich repeats flanked by a N- and C-terminal leucine rich repeat domain, a membrane-spanning region, and an intracellular TIR domain. The receptor is phylogenetically most similar to TLR5 of birds and most distant to fish TLR5. Transcript analysis revealed acTLR5 expression in multiple lizard tissues. Stimulation of acTLR5 with TLR ligands demonstrated unique responsiveness towards bacterial flagellin in both reptile and human cells. Comparison of acTLR5 and human TLR5 using purified flagellins revealed differential sensitivity to Pseudomonas but not Salmonella flagellin, indicating development of species-specific flagellin recognition during the divergent evolution of mammals and reptiles. Our discovery of reptile TLR5 fills the evolutionary gap regarding TLR conservation across vertebrates and provides novel insights in functional evolution of host-microbe interactions.
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spelling pubmed-47039532016-01-19 Reptile Toll-like receptor 5 unveils adaptive evolution of bacterial flagellin recognition Voogdt, Carlos G. P. Bouwman, Lieneke I. Kik, Marja J. L. Wagenaar, Jaap A. van Putten, Jos P. M. Sci Rep Article Toll-like receptors (TLR) are ancient innate immune receptors crucial for immune homeostasis and protection against infection. TLRs are present in mammals, birds, amphibians and fish but have not been functionally characterized in reptiles despite the central position of this animal class in vertebrate evolution. Here we report the cloning, characterization, and function of TLR5 of the reptile Anolis carolinensis (Green Anole lizard). The receptor (acTLR5) displays the typical TLR protein architecture with 22 extracellular leucine rich repeats flanked by a N- and C-terminal leucine rich repeat domain, a membrane-spanning region, and an intracellular TIR domain. The receptor is phylogenetically most similar to TLR5 of birds and most distant to fish TLR5. Transcript analysis revealed acTLR5 expression in multiple lizard tissues. Stimulation of acTLR5 with TLR ligands demonstrated unique responsiveness towards bacterial flagellin in both reptile and human cells. Comparison of acTLR5 and human TLR5 using purified flagellins revealed differential sensitivity to Pseudomonas but not Salmonella flagellin, indicating development of species-specific flagellin recognition during the divergent evolution of mammals and reptiles. Our discovery of reptile TLR5 fills the evolutionary gap regarding TLR conservation across vertebrates and provides novel insights in functional evolution of host-microbe interactions. Nature Publishing Group 2016-01-07 /pmc/articles/PMC4703953/ /pubmed/26738735 http://dx.doi.org/10.1038/srep19046 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Voogdt, Carlos G. P.
Bouwman, Lieneke I.
Kik, Marja J. L.
Wagenaar, Jaap A.
van Putten, Jos P. M.
Reptile Toll-like receptor 5 unveils adaptive evolution of bacterial flagellin recognition
title Reptile Toll-like receptor 5 unveils adaptive evolution of bacterial flagellin recognition
title_full Reptile Toll-like receptor 5 unveils adaptive evolution of bacterial flagellin recognition
title_fullStr Reptile Toll-like receptor 5 unveils adaptive evolution of bacterial flagellin recognition
title_full_unstemmed Reptile Toll-like receptor 5 unveils adaptive evolution of bacterial flagellin recognition
title_short Reptile Toll-like receptor 5 unveils adaptive evolution of bacterial flagellin recognition
title_sort reptile toll-like receptor 5 unveils adaptive evolution of bacterial flagellin recognition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4703953/
https://www.ncbi.nlm.nih.gov/pubmed/26738735
http://dx.doi.org/10.1038/srep19046
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