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Characterisation and functional analysis of canine TLR5
In this study, we characterised the single exon TLR5 gene of the Chinese rural dog. Sequence analysis revealed a 2577 nucleotide-long open reading frame of canine TLR5, encoding an 858 amino acid-long protein. The putative amino acid sequence of canine TLR5 consisted of a signal peptide sequence, 15...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7491235/ https://www.ncbi.nlm.nih.gov/pubmed/31986950 http://dx.doi.org/10.1177/1753425920901862 |
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author | Zhu, Aihua Wei, Lingling Hu, Sujuan Yang, Cheng Chen, Caifa Zhou, Zhengkun Pan, Zhiming |
author_facet | Zhu, Aihua Wei, Lingling Hu, Sujuan Yang, Cheng Chen, Caifa Zhou, Zhengkun Pan, Zhiming |
author_sort | Zhu, Aihua |
collection | PubMed |
description | In this study, we characterised the single exon TLR5 gene of the Chinese rural dog. Sequence analysis revealed a 2577 nucleotide-long open reading frame of canine TLR5, encoding an 858 amino acid-long protein. The putative amino acid sequence of canine TLR5 consisted of a signal peptide sequence, 15 LRR domains, a LRR C-terminal domain, a transmembrane domain and an intracellular Toll-IL-1 receptor domain. The amino acid sequence of the canine TLR5 protein shared 95.4% identity with vulpine, 72.2% with feline and 64.7% with human TLR5. Plasmids expressing canine TLR5 and NF-κB-luciferase were constructed and transfected into HEK293T cells. Expression was confirmed by indirect immunofluorescence assay. These HEK293T cells transfected with the canine TLR5- and NF-κB-luciferase plasmids significantly responded to flagellin from Salmonella enteritidis serovar Typhimurium, indicating that it is a functional TLR5 homolog. In response to stimulation with Salmonella enteritidis, the level of TLR5 mRNA significantly increased over the control in PBMCs at 4 h. The levels of IL-8, IL-6 and IL-1β also increased after exposure. The highest levels of TLR5, IL-8 and IL-1β expression were detected at 8, 4 and 12 h after stimulation, respectively. These results imply that the expression of canine TLR5 may participate in the immune response against bacterial pathogens. |
format | Online Article Text |
id | pubmed-7491235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-74912352020-09-23 Characterisation and functional analysis of canine TLR5 Zhu, Aihua Wei, Lingling Hu, Sujuan Yang, Cheng Chen, Caifa Zhou, Zhengkun Pan, Zhiming Innate Immun Original Articles In this study, we characterised the single exon TLR5 gene of the Chinese rural dog. Sequence analysis revealed a 2577 nucleotide-long open reading frame of canine TLR5, encoding an 858 amino acid-long protein. The putative amino acid sequence of canine TLR5 consisted of a signal peptide sequence, 15 LRR domains, a LRR C-terminal domain, a transmembrane domain and an intracellular Toll-IL-1 receptor domain. The amino acid sequence of the canine TLR5 protein shared 95.4% identity with vulpine, 72.2% with feline and 64.7% with human TLR5. Plasmids expressing canine TLR5 and NF-κB-luciferase were constructed and transfected into HEK293T cells. Expression was confirmed by indirect immunofluorescence assay. These HEK293T cells transfected with the canine TLR5- and NF-κB-luciferase plasmids significantly responded to flagellin from Salmonella enteritidis serovar Typhimurium, indicating that it is a functional TLR5 homolog. In response to stimulation with Salmonella enteritidis, the level of TLR5 mRNA significantly increased over the control in PBMCs at 4 h. The levels of IL-8, IL-6 and IL-1β also increased after exposure. The highest levels of TLR5, IL-8 and IL-1β expression were detected at 8, 4 and 12 h after stimulation, respectively. These results imply that the expression of canine TLR5 may participate in the immune response against bacterial pathogens. SAGE Publications 2020-01-27 2020-08 /pmc/articles/PMC7491235/ /pubmed/31986950 http://dx.doi.org/10.1177/1753425920901862 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Zhu, Aihua Wei, Lingling Hu, Sujuan Yang, Cheng Chen, Caifa Zhou, Zhengkun Pan, Zhiming Characterisation and functional analysis of canine TLR5 |
title | Characterisation and functional analysis of canine TLR5 |
title_full | Characterisation and functional analysis of canine TLR5 |
title_fullStr | Characterisation and functional analysis of canine TLR5 |
title_full_unstemmed | Characterisation and functional analysis of canine TLR5 |
title_short | Characterisation and functional analysis of canine TLR5 |
title_sort | characterisation and functional analysis of canine tlr5 |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7491235/ https://www.ncbi.nlm.nih.gov/pubmed/31986950 http://dx.doi.org/10.1177/1753425920901862 |
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