Cargando…

Protective Role of Rabbit Nucleotide-Binding Oligomerization Domain-2 (NOD2)-Mediated Signaling Pathway in Resistance to Enterohemorrhagic Escherichia coli Infection

Nucleotide-binding oligomerization domain 2 (NOD2), a member of the NOD-like receptors (NLRs) family that is well-known to play a key role in innate immune responses and is involved in innate antibacterial responses. In this study, rabbit NOD2 (rNOD2) was cloned from rabbit kidney (RK) cells. It was...

Descripción completa

Detalles Bibliográficos
Autores principales: Guo, Mengjiao, Li, Rong, Xiao, Qianqian, Fan, Xiuxiu, Li, Ning, Shang, Yingli, Wei, Liangmeng, Chai, Tongjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031198/
https://www.ncbi.nlm.nih.gov/pubmed/29998088
http://dx.doi.org/10.3389/fcimb.2018.00220
_version_ 1783337273163513856
author Guo, Mengjiao
Li, Rong
Xiao, Qianqian
Fan, Xiuxiu
Li, Ning
Shang, Yingli
Wei, Liangmeng
Chai, Tongjie
author_facet Guo, Mengjiao
Li, Rong
Xiao, Qianqian
Fan, Xiuxiu
Li, Ning
Shang, Yingli
Wei, Liangmeng
Chai, Tongjie
author_sort Guo, Mengjiao
collection PubMed
description Nucleotide-binding oligomerization domain 2 (NOD2), a member of the NOD-like receptors (NLRs) family that is well-known to play a key role in innate immune responses and is involved in innate antibacterial responses. In this study, rabbit NOD2 (rNOD2) was cloned from rabbit kidney (RK) cells. It was distributed in various tissues, and the highest level of rNod2 was detected in spleen. Moreover, the expression of rNod2 was significantly upregulated in the heart, liver, and spleen induced by enterohemorrhagic Escherichia coli (EHEC). Overexpression of rNOD2 induced the expression of pro-inflammatory cytokine, including Il1β, Il6, Ifn-γ, and Tnf, as well as defensins, including Defb124, Defb125, and Defb128 through the nuclear factor (NF)-κB signaling pathway. Furthermore, overexpression of rNOD2 inhibited the growth of EHEC, and knockdown of rNOD2 or inhibition of the NF-κB pathway promoted its replication. In addition, our results suggest that rNOD2 can significantly activate NF-κB signaling and trigger antibacterial defenses to increase the expression of pro-inflammatory cytokine and defensins after stimulation by EHEC. These findings are useful to further understanding the innate immune system of rabbits and providing a new perspective for the prevention of bacterial diseases in rabbits.
format Online
Article
Text
id pubmed-6031198
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-60311982018-07-11 Protective Role of Rabbit Nucleotide-Binding Oligomerization Domain-2 (NOD2)-Mediated Signaling Pathway in Resistance to Enterohemorrhagic Escherichia coli Infection Guo, Mengjiao Li, Rong Xiao, Qianqian Fan, Xiuxiu Li, Ning Shang, Yingli Wei, Liangmeng Chai, Tongjie Front Cell Infect Microbiol Cellular and Infection Microbiology Nucleotide-binding oligomerization domain 2 (NOD2), a member of the NOD-like receptors (NLRs) family that is well-known to play a key role in innate immune responses and is involved in innate antibacterial responses. In this study, rabbit NOD2 (rNOD2) was cloned from rabbit kidney (RK) cells. It was distributed in various tissues, and the highest level of rNod2 was detected in spleen. Moreover, the expression of rNod2 was significantly upregulated in the heart, liver, and spleen induced by enterohemorrhagic Escherichia coli (EHEC). Overexpression of rNOD2 induced the expression of pro-inflammatory cytokine, including Il1β, Il6, Ifn-γ, and Tnf, as well as defensins, including Defb124, Defb125, and Defb128 through the nuclear factor (NF)-κB signaling pathway. Furthermore, overexpression of rNOD2 inhibited the growth of EHEC, and knockdown of rNOD2 or inhibition of the NF-κB pathway promoted its replication. In addition, our results suggest that rNOD2 can significantly activate NF-κB signaling and trigger antibacterial defenses to increase the expression of pro-inflammatory cytokine and defensins after stimulation by EHEC. These findings are useful to further understanding the innate immune system of rabbits and providing a new perspective for the prevention of bacterial diseases in rabbits. Frontiers Media S.A. 2018-06-26 /pmc/articles/PMC6031198/ /pubmed/29998088 http://dx.doi.org/10.3389/fcimb.2018.00220 Text en Copyright © 2018 Guo, Li, Xiao, Fan, Li, Shang, Wei and Chai. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Guo, Mengjiao
Li, Rong
Xiao, Qianqian
Fan, Xiuxiu
Li, Ning
Shang, Yingli
Wei, Liangmeng
Chai, Tongjie
Protective Role of Rabbit Nucleotide-Binding Oligomerization Domain-2 (NOD2)-Mediated Signaling Pathway in Resistance to Enterohemorrhagic Escherichia coli Infection
title Protective Role of Rabbit Nucleotide-Binding Oligomerization Domain-2 (NOD2)-Mediated Signaling Pathway in Resistance to Enterohemorrhagic Escherichia coli Infection
title_full Protective Role of Rabbit Nucleotide-Binding Oligomerization Domain-2 (NOD2)-Mediated Signaling Pathway in Resistance to Enterohemorrhagic Escherichia coli Infection
title_fullStr Protective Role of Rabbit Nucleotide-Binding Oligomerization Domain-2 (NOD2)-Mediated Signaling Pathway in Resistance to Enterohemorrhagic Escherichia coli Infection
title_full_unstemmed Protective Role of Rabbit Nucleotide-Binding Oligomerization Domain-2 (NOD2)-Mediated Signaling Pathway in Resistance to Enterohemorrhagic Escherichia coli Infection
title_short Protective Role of Rabbit Nucleotide-Binding Oligomerization Domain-2 (NOD2)-Mediated Signaling Pathway in Resistance to Enterohemorrhagic Escherichia coli Infection
title_sort protective role of rabbit nucleotide-binding oligomerization domain-2 (nod2)-mediated signaling pathway in resistance to enterohemorrhagic escherichia coli infection
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031198/
https://www.ncbi.nlm.nih.gov/pubmed/29998088
http://dx.doi.org/10.3389/fcimb.2018.00220
work_keys_str_mv AT guomengjiao protectiveroleofrabbitnucleotidebindingoligomerizationdomain2nod2mediatedsignalingpathwayinresistancetoenterohemorrhagicescherichiacoliinfection
AT lirong protectiveroleofrabbitnucleotidebindingoligomerizationdomain2nod2mediatedsignalingpathwayinresistancetoenterohemorrhagicescherichiacoliinfection
AT xiaoqianqian protectiveroleofrabbitnucleotidebindingoligomerizationdomain2nod2mediatedsignalingpathwayinresistancetoenterohemorrhagicescherichiacoliinfection
AT fanxiuxiu protectiveroleofrabbitnucleotidebindingoligomerizationdomain2nod2mediatedsignalingpathwayinresistancetoenterohemorrhagicescherichiacoliinfection
AT lining protectiveroleofrabbitnucleotidebindingoligomerizationdomain2nod2mediatedsignalingpathwayinresistancetoenterohemorrhagicescherichiacoliinfection
AT shangyingli protectiveroleofrabbitnucleotidebindingoligomerizationdomain2nod2mediatedsignalingpathwayinresistancetoenterohemorrhagicescherichiacoliinfection
AT weiliangmeng protectiveroleofrabbitnucleotidebindingoligomerizationdomain2nod2mediatedsignalingpathwayinresistancetoenterohemorrhagicescherichiacoliinfection
AT chaitongjie protectiveroleofrabbitnucleotidebindingoligomerizationdomain2nod2mediatedsignalingpathwayinresistancetoenterohemorrhagicescherichiacoliinfection