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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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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 |
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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 |
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