Functional characterization of chicken TLR5 reveals species-specific recognition of flagellin

Mammalian Toll-like receptor 5 (TLR5) senses flagellin of several bacterial species and activates the innate immune system. The avian TLR repertoire exhibits considerable functional diversity compared to mammalian TLRs and evidence of a functional TLR5 in the avian species is lacking. In the present...

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Veröffentlicht in:Molecular immunology 2008-03, Vol.45 (5), p.1298-1307
Hauptverfasser: Keestra, A. Marijke, de Zoete, Marcel R., van Aubel, Rémon A.M.H., van Putten, Jos P.M.
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container_end_page 1307
container_issue 5
container_start_page 1298
container_title Molecular immunology
container_volume 45
creator Keestra, A. Marijke
de Zoete, Marcel R.
van Aubel, Rémon A.M.H.
van Putten, Jos P.M.
description Mammalian Toll-like receptor 5 (TLR5) senses flagellin of several bacterial species and activates the innate immune system. The avian TLR repertoire exhibits considerable functional diversity compared to mammalian TLRs and evidence of a functional TLR5 in the avian species is lacking. In the present study we cloned and successfully expressed chicken TLR5 (chTLR5) in HeLa cells, as indicated by laser confocal microscopy. Infection of chTLR5 transfected cells with Salmonella enterica serovar Enteritidis activated NF-κB in a dose- and flagellin-dependent fashion. Similar NF-κB activation was observed with recombinant bacterial flagellin. Targeted mutagenesis of the proline residue at position 737 in the chTLR5-TIR domain was detrimental to chTLR5 function, confirming that the observed effects were conferred via chTLR5 and the MyD88 signaling pathway. Comparison of human, mouse and chicken TLR5 activation by flagellin of S. enterica serovar Typhimurium revealed that chTLR5 consistently yielded stronger responses than human but not mouse TLR5. This species-specific reactivity was not observed with flagellin of serovar Enteritidis. The species-specific TLR5 response was nullified after targeted mutagenesis of a single amino acid (Q89A) in serovar Typhimurium flagellin, while L415A and N100A substitutions had no effect. These results show that chickens express a functional TLR5 albeit with different flagellin sensing qualities compared to human TLR5. The finding that single amino acid substitutions in bacterial flagellin can alter the species-specific TLR5 response may influence the host range and susceptibility of infection.
doi_str_mv 10.1016/j.molimm.2007.09.013
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Targeted mutagenesis of the proline residue at position 737 in the chTLR5-TIR domain was detrimental to chTLR5 function, confirming that the observed effects were conferred via chTLR5 and the MyD88 signaling pathway. Comparison of human, mouse and chicken TLR5 activation by flagellin of S. enterica serovar Typhimurium revealed that chTLR5 consistently yielded stronger responses than human but not mouse TLR5. This species-specific reactivity was not observed with flagellin of serovar Enteritidis. The species-specific TLR5 response was nullified after targeted mutagenesis of a single amino acid (Q89A) in serovar Typhimurium flagellin, while L415A and N100A substitutions had no effect. These results show that chickens express a functional TLR5 albeit with different flagellin sensing qualities compared to human TLR5. 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subjects Animals
Base Sequence
Chicken
Chickens
Cloning, Molecular
Evolution
Flagellin
Flagellin - metabolism
Genetic Predisposition to Disease
HeLa Cells
Humans
Molecular Sequence Data
Mutation, Missense
NF-kappa B - metabolism
NF-κB
Protein Binding - genetics
Salmonella enterica
Salmonella enteritidis - immunology
Species Specificity
Toll-like receptor
Toll-Like Receptor 5 - genetics
Toll-Like Receptor 5 - immunology
Toll-Like Receptor 5 - metabolism
Transfection
title Functional characterization of chicken TLR5 reveals species-specific recognition of flagellin
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