Cargando…

Mycoplasma hyopneumoniae J elicits an antioxidant response and decreases the expression of ciliary genes in infected swine epithelial cells

Mycoplasma hyopneumoniae is the most costly pathogen for swine production. Although several studies have focused on the host-bacterium association, little is known about the changes in gene expression of swine cells upon infection. To improve our understanding of this interaction, we infected swine...

Descripción completa

Detalles Bibliográficos
Autores principales: Mucha, Scheila G., Ferrarini, Mariana G., Moraga, Carol, Di Genova, Alex, Guyon, Laurent, Tardy, Florence, Rome, Sophie, Sagot, Marie-France, Zaha, Arnaldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426424/
https://www.ncbi.nlm.nih.gov/pubmed/32792522
http://dx.doi.org/10.1038/s41598-020-70040-y
_version_ 1783570680232542208
author Mucha, Scheila G.
Ferrarini, Mariana G.
Moraga, Carol
Di Genova, Alex
Guyon, Laurent
Tardy, Florence
Rome, Sophie
Sagot, Marie-France
Zaha, Arnaldo
author_facet Mucha, Scheila G.
Ferrarini, Mariana G.
Moraga, Carol
Di Genova, Alex
Guyon, Laurent
Tardy, Florence
Rome, Sophie
Sagot, Marie-France
Zaha, Arnaldo
author_sort Mucha, Scheila G.
collection PubMed
description Mycoplasma hyopneumoniae is the most costly pathogen for swine production. Although several studies have focused on the host-bacterium association, little is known about the changes in gene expression of swine cells upon infection. To improve our understanding of this interaction, we infected swine epithelial NPTr cells with M. hyopneumoniae strain J to identify differentially expressed mRNAs and miRNAs. The levels of 1,268 genes and 170 miRNAs were significantly modified post-infection. Up-regulated mRNAs were enriched in genes related to redox homeostasis and antioxidant defense, known to be regulated by the transcription factor NRF2 in related species. Down-regulated mRNAs were enriched in genes associated with cytoskeleton and ciliary functions. Bioinformatic analyses suggested a correlation between changes in miRNA and mRNA levels, since we detected down-regulation of miRNAs predicted to target antioxidant genes and up-regulation of miRNAs targeting ciliary and cytoskeleton genes. Interestingly, most down-regulated miRNAs were detected in exosome-like vesicles suggesting that M. hyopneumoniae infection induced a modification of the composition of NPTr-released vesicles. Taken together, our data indicate that M. hyopneumoniae elicits an antioxidant response induced by NRF2 in infected cells. In addition, we propose that ciliostasis caused by this pathogen is partially explained by the down-regulation of ciliary genes.
format Online
Article
Text
id pubmed-7426424
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-74264242020-08-14 Mycoplasma hyopneumoniae J elicits an antioxidant response and decreases the expression of ciliary genes in infected swine epithelial cells Mucha, Scheila G. Ferrarini, Mariana G. Moraga, Carol Di Genova, Alex Guyon, Laurent Tardy, Florence Rome, Sophie Sagot, Marie-France Zaha, Arnaldo Sci Rep Article Mycoplasma hyopneumoniae is the most costly pathogen for swine production. Although several studies have focused on the host-bacterium association, little is known about the changes in gene expression of swine cells upon infection. To improve our understanding of this interaction, we infected swine epithelial NPTr cells with M. hyopneumoniae strain J to identify differentially expressed mRNAs and miRNAs. The levels of 1,268 genes and 170 miRNAs were significantly modified post-infection. Up-regulated mRNAs were enriched in genes related to redox homeostasis and antioxidant defense, known to be regulated by the transcription factor NRF2 in related species. Down-regulated mRNAs were enriched in genes associated with cytoskeleton and ciliary functions. Bioinformatic analyses suggested a correlation between changes in miRNA and mRNA levels, since we detected down-regulation of miRNAs predicted to target antioxidant genes and up-regulation of miRNAs targeting ciliary and cytoskeleton genes. Interestingly, most down-regulated miRNAs were detected in exosome-like vesicles suggesting that M. hyopneumoniae infection induced a modification of the composition of NPTr-released vesicles. Taken together, our data indicate that M. hyopneumoniae elicits an antioxidant response induced by NRF2 in infected cells. In addition, we propose that ciliostasis caused by this pathogen is partially explained by the down-regulation of ciliary genes. Nature Publishing Group UK 2020-08-13 /pmc/articles/PMC7426424/ /pubmed/32792522 http://dx.doi.org/10.1038/s41598-020-70040-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mucha, Scheila G.
Ferrarini, Mariana G.
Moraga, Carol
Di Genova, Alex
Guyon, Laurent
Tardy, Florence
Rome, Sophie
Sagot, Marie-France
Zaha, Arnaldo
Mycoplasma hyopneumoniae J elicits an antioxidant response and decreases the expression of ciliary genes in infected swine epithelial cells
title Mycoplasma hyopneumoniae J elicits an antioxidant response and decreases the expression of ciliary genes in infected swine epithelial cells
title_full Mycoplasma hyopneumoniae J elicits an antioxidant response and decreases the expression of ciliary genes in infected swine epithelial cells
title_fullStr Mycoplasma hyopneumoniae J elicits an antioxidant response and decreases the expression of ciliary genes in infected swine epithelial cells
title_full_unstemmed Mycoplasma hyopneumoniae J elicits an antioxidant response and decreases the expression of ciliary genes in infected swine epithelial cells
title_short Mycoplasma hyopneumoniae J elicits an antioxidant response and decreases the expression of ciliary genes in infected swine epithelial cells
title_sort mycoplasma hyopneumoniae j elicits an antioxidant response and decreases the expression of ciliary genes in infected swine epithelial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426424/
https://www.ncbi.nlm.nih.gov/pubmed/32792522
http://dx.doi.org/10.1038/s41598-020-70040-y
work_keys_str_mv AT muchascheilag mycoplasmahyopneumoniaejelicitsanantioxidantresponseanddecreasestheexpressionofciliarygenesininfectedswineepithelialcells
AT ferrarinimarianag mycoplasmahyopneumoniaejelicitsanantioxidantresponseanddecreasestheexpressionofciliarygenesininfectedswineepithelialcells
AT moragacarol mycoplasmahyopneumoniaejelicitsanantioxidantresponseanddecreasestheexpressionofciliarygenesininfectedswineepithelialcells
AT digenovaalex mycoplasmahyopneumoniaejelicitsanantioxidantresponseanddecreasestheexpressionofciliarygenesininfectedswineepithelialcells
AT guyonlaurent mycoplasmahyopneumoniaejelicitsanantioxidantresponseanddecreasestheexpressionofciliarygenesininfectedswineepithelialcells
AT tardyflorence mycoplasmahyopneumoniaejelicitsanantioxidantresponseanddecreasestheexpressionofciliarygenesininfectedswineepithelialcells
AT romesophie mycoplasmahyopneumoniaejelicitsanantioxidantresponseanddecreasestheexpressionofciliarygenesininfectedswineepithelialcells
AT sagotmariefrance mycoplasmahyopneumoniaejelicitsanantioxidantresponseanddecreasestheexpressionofciliarygenesininfectedswineepithelialcells
AT zahaarnaldo mycoplasmahyopneumoniaejelicitsanantioxidantresponseanddecreasestheexpressionofciliarygenesininfectedswineepithelialcells