Cargando…

Mycoplasma hyopneumoniae Infection Activates the NOD1 Signaling Pathway to Modulate Inflammation

Mycoplasma hyopneumoniae is a highly contagious pathogen causing porcine enzootic pneumonia, which elicits prolonged inflammatory response modulated by pattern recognition receptors (PRRs). Although significant advances have been achieved in understanding the Toll-Like receptors that recognize M. hy...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Wei, Jiang, Pengcheng, Yang, Keli, Song, Qiqi, Yuan, Fangyan, Liu, Zewen, Gao, Ting, Zhou, Danna, Guo, Rui, Li, Chang, Sun, Pei, Tian, Yongxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304885/
https://www.ncbi.nlm.nih.gov/pubmed/35873172
http://dx.doi.org/10.3389/fcimb.2022.927840
_version_ 1784752191884492800
author Liu, Wei
Jiang, Pengcheng
Yang, Keli
Song, Qiqi
Yuan, Fangyan
Liu, Zewen
Gao, Ting
Zhou, Danna
Guo, Rui
Li, Chang
Sun, Pei
Tian, Yongxiang
author_facet Liu, Wei
Jiang, Pengcheng
Yang, Keli
Song, Qiqi
Yuan, Fangyan
Liu, Zewen
Gao, Ting
Zhou, Danna
Guo, Rui
Li, Chang
Sun, Pei
Tian, Yongxiang
author_sort Liu, Wei
collection PubMed
description Mycoplasma hyopneumoniae is a highly contagious pathogen causing porcine enzootic pneumonia, which elicits prolonged inflammatory response modulated by pattern recognition receptors (PRRs). Although significant advances have been achieved in understanding the Toll-Like receptors that recognize M. hyopneumoniae, the role of nucleotide-binding oligomerization domain 1 (NOD1) in M. hyopneumoniae infected cells remains poorly understood. This study revealed that M. hyopneumoniae activates the NOD1-RIP2 pathway and is co-localized with host NOD1 during infection. siRNA knockdown of NOD1 significantly impaired the TRIF and MYD88 pathway and blocked the activation of TNF-α. In contrast, NOD1 overexpression significantly suppressed M. hyopneumoniae proliferation. Furthermore, we for the first time investigated the interaction between M. hyopneumoniae mhp390 and NOD1 receptor, and the results suggested that mhp390 and NOD1 are possibly involved in the recognition of M. hyopneumoniae. These findings may improve our understanding of the interaction between PRRs and M. hyopneumoniae and the function of NOD1 in host defense against M. hyopneumoniae infection.
format Online
Article
Text
id pubmed-9304885
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-93048852022-07-23 Mycoplasma hyopneumoniae Infection Activates the NOD1 Signaling Pathway to Modulate Inflammation Liu, Wei Jiang, Pengcheng Yang, Keli Song, Qiqi Yuan, Fangyan Liu, Zewen Gao, Ting Zhou, Danna Guo, Rui Li, Chang Sun, Pei Tian, Yongxiang Front Cell Infect Microbiol Cellular and Infection Microbiology Mycoplasma hyopneumoniae is a highly contagious pathogen causing porcine enzootic pneumonia, which elicits prolonged inflammatory response modulated by pattern recognition receptors (PRRs). Although significant advances have been achieved in understanding the Toll-Like receptors that recognize M. hyopneumoniae, the role of nucleotide-binding oligomerization domain 1 (NOD1) in M. hyopneumoniae infected cells remains poorly understood. This study revealed that M. hyopneumoniae activates the NOD1-RIP2 pathway and is co-localized with host NOD1 during infection. siRNA knockdown of NOD1 significantly impaired the TRIF and MYD88 pathway and blocked the activation of TNF-α. In contrast, NOD1 overexpression significantly suppressed M. hyopneumoniae proliferation. Furthermore, we for the first time investigated the interaction between M. hyopneumoniae mhp390 and NOD1 receptor, and the results suggested that mhp390 and NOD1 are possibly involved in the recognition of M. hyopneumoniae. These findings may improve our understanding of the interaction between PRRs and M. hyopneumoniae and the function of NOD1 in host defense against M. hyopneumoniae infection. Frontiers Media S.A. 2022-07-08 /pmc/articles/PMC9304885/ /pubmed/35873172 http://dx.doi.org/10.3389/fcimb.2022.927840 Text en Copyright © 2022 Liu, Jiang, Yang, Song, Yuan, Liu, Gao, Zhou, Guo, Li, Sun and Tian https://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(s) 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
Liu, Wei
Jiang, Pengcheng
Yang, Keli
Song, Qiqi
Yuan, Fangyan
Liu, Zewen
Gao, Ting
Zhou, Danna
Guo, Rui
Li, Chang
Sun, Pei
Tian, Yongxiang
Mycoplasma hyopneumoniae Infection Activates the NOD1 Signaling Pathway to Modulate Inflammation
title Mycoplasma hyopneumoniae Infection Activates the NOD1 Signaling Pathway to Modulate Inflammation
title_full Mycoplasma hyopneumoniae Infection Activates the NOD1 Signaling Pathway to Modulate Inflammation
title_fullStr Mycoplasma hyopneumoniae Infection Activates the NOD1 Signaling Pathway to Modulate Inflammation
title_full_unstemmed Mycoplasma hyopneumoniae Infection Activates the NOD1 Signaling Pathway to Modulate Inflammation
title_short Mycoplasma hyopneumoniae Infection Activates the NOD1 Signaling Pathway to Modulate Inflammation
title_sort mycoplasma hyopneumoniae infection activates the nod1 signaling pathway to modulate inflammation
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304885/
https://www.ncbi.nlm.nih.gov/pubmed/35873172
http://dx.doi.org/10.3389/fcimb.2022.927840
work_keys_str_mv AT liuwei mycoplasmahyopneumoniaeinfectionactivatesthenod1signalingpathwaytomodulateinflammation
AT jiangpengcheng mycoplasmahyopneumoniaeinfectionactivatesthenod1signalingpathwaytomodulateinflammation
AT yangkeli mycoplasmahyopneumoniaeinfectionactivatesthenod1signalingpathwaytomodulateinflammation
AT songqiqi mycoplasmahyopneumoniaeinfectionactivatesthenod1signalingpathwaytomodulateinflammation
AT yuanfangyan mycoplasmahyopneumoniaeinfectionactivatesthenod1signalingpathwaytomodulateinflammation
AT liuzewen mycoplasmahyopneumoniaeinfectionactivatesthenod1signalingpathwaytomodulateinflammation
AT gaoting mycoplasmahyopneumoniaeinfectionactivatesthenod1signalingpathwaytomodulateinflammation
AT zhoudanna mycoplasmahyopneumoniaeinfectionactivatesthenod1signalingpathwaytomodulateinflammation
AT guorui mycoplasmahyopneumoniaeinfectionactivatesthenod1signalingpathwaytomodulateinflammation
AT lichang mycoplasmahyopneumoniaeinfectionactivatesthenod1signalingpathwaytomodulateinflammation
AT sunpei mycoplasmahyopneumoniaeinfectionactivatesthenod1signalingpathwaytomodulateinflammation
AT tianyongxiang mycoplasmahyopneumoniaeinfectionactivatesthenod1signalingpathwaytomodulateinflammation