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Late regulation of immune genes and microRNAs in circulating leukocytes in a pig model of influenza A (H1N2) infection
MicroRNAs (miRNAs) are a class of short regulatory RNA molecules which are implicated in modulating gene expression. Levels of circulating, cell-associated miRNAs in response to influenza A virus (IAV) infection has received limited attention so far. To further understand the temporal dynamics and b...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759598/ https://www.ncbi.nlm.nih.gov/pubmed/26893019 http://dx.doi.org/10.1038/srep21812 |
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author | Brogaard, Louise Heegaard, Peter M. H. Larsen, Lars E. Mortensen, Shila Schlegel, Michael Dürrwald, Ralf Skovgaard, Kerstin |
author_facet | Brogaard, Louise Heegaard, Peter M. H. Larsen, Lars E. Mortensen, Shila Schlegel, Michael Dürrwald, Ralf Skovgaard, Kerstin |
author_sort | Brogaard, Louise |
collection | PubMed |
description | MicroRNAs (miRNAs) are a class of short regulatory RNA molecules which are implicated in modulating gene expression. Levels of circulating, cell-associated miRNAs in response to influenza A virus (IAV) infection has received limited attention so far. To further understand the temporal dynamics and biological implications of miRNA regulation in circulating leukocytes, we collected blood samples before and after (1, 3, and 14 days) IAV challenge of pigs. Differential expression of miRNAs and innate immune factor mRNA transcripts was analysed using RT-qPCR. A total of 20 miRNAs were regulated after IAV challenge, with the highest number of regulated miRNAs seen on day 14 after infection at which time the infection was cleared. Targets of the regulated miRNAs included genes involved in apoptosis and cell cycle regulation. Significant regulation of both miRNAs and mRNA transcripts at 14 days after challenge points to a protracted effect of IAV infection, potentially affecting the host’s ability to respond to secondary infections. In conclusion, experimental IAV infection of pigs demonstrated the dynamic nature of miRNA and mRNA regulation in circulating leukocytes during and after infection, and revealed the need for further investigation of the potential immunosuppressing effect of miRNA and innate immune signaling after IAV infection. |
format | Online Article Text |
id | pubmed-4759598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47595982016-02-29 Late regulation of immune genes and microRNAs in circulating leukocytes in a pig model of influenza A (H1N2) infection Brogaard, Louise Heegaard, Peter M. H. Larsen, Lars E. Mortensen, Shila Schlegel, Michael Dürrwald, Ralf Skovgaard, Kerstin Sci Rep Article MicroRNAs (miRNAs) are a class of short regulatory RNA molecules which are implicated in modulating gene expression. Levels of circulating, cell-associated miRNAs in response to influenza A virus (IAV) infection has received limited attention so far. To further understand the temporal dynamics and biological implications of miRNA regulation in circulating leukocytes, we collected blood samples before and after (1, 3, and 14 days) IAV challenge of pigs. Differential expression of miRNAs and innate immune factor mRNA transcripts was analysed using RT-qPCR. A total of 20 miRNAs were regulated after IAV challenge, with the highest number of regulated miRNAs seen on day 14 after infection at which time the infection was cleared. Targets of the regulated miRNAs included genes involved in apoptosis and cell cycle regulation. Significant regulation of both miRNAs and mRNA transcripts at 14 days after challenge points to a protracted effect of IAV infection, potentially affecting the host’s ability to respond to secondary infections. In conclusion, experimental IAV infection of pigs demonstrated the dynamic nature of miRNA and mRNA regulation in circulating leukocytes during and after infection, and revealed the need for further investigation of the potential immunosuppressing effect of miRNA and innate immune signaling after IAV infection. Nature Publishing Group 2016-02-19 /pmc/articles/PMC4759598/ /pubmed/26893019 http://dx.doi.org/10.1038/srep21812 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Brogaard, Louise Heegaard, Peter M. H. Larsen, Lars E. Mortensen, Shila Schlegel, Michael Dürrwald, Ralf Skovgaard, Kerstin Late regulation of immune genes and microRNAs in circulating leukocytes in a pig model of influenza A (H1N2) infection |
title | Late regulation of immune genes and microRNAs in circulating leukocytes in a pig model of influenza A (H1N2) infection |
title_full | Late regulation of immune genes and microRNAs in circulating leukocytes in a pig model of influenza A (H1N2) infection |
title_fullStr | Late regulation of immune genes and microRNAs in circulating leukocytes in a pig model of influenza A (H1N2) infection |
title_full_unstemmed | Late regulation of immune genes and microRNAs in circulating leukocytes in a pig model of influenza A (H1N2) infection |
title_short | Late regulation of immune genes and microRNAs in circulating leukocytes in a pig model of influenza A (H1N2) infection |
title_sort | late regulation of immune genes and micrornas in circulating leukocytes in a pig model of influenza a (h1n2) infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759598/ https://www.ncbi.nlm.nih.gov/pubmed/26893019 http://dx.doi.org/10.1038/srep21812 |
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