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Genes Involved in miRNA Biogenesis Are Not Downregulated in SARS-CoV-2 Infection
miRNAs, small non-coding RNAs that regulate gene expression, are involved in various pathological processes, including viral infections. Virus infections may interfere with the miRNA pathway through the inhibition of genes involved in miRNA biogenesis. A reduction in the number and the levels of miR...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222706/ https://www.ncbi.nlm.nih.gov/pubmed/37243263 http://dx.doi.org/10.3390/v15051177 |
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author | Garnier, Nathalie Sane, Famara Massara, Layal Soncin, Fabrice Gosset, Philippe Hober, Didier Szunerits, Sabine Engelmann, Ilka |
author_facet | Garnier, Nathalie Sane, Famara Massara, Layal Soncin, Fabrice Gosset, Philippe Hober, Didier Szunerits, Sabine Engelmann, Ilka |
author_sort | Garnier, Nathalie |
collection | PubMed |
description | miRNAs, small non-coding RNAs that regulate gene expression, are involved in various pathological processes, including viral infections. Virus infections may interfere with the miRNA pathway through the inhibition of genes involved in miRNA biogenesis. A reduction in the number and the levels of miRNAs expressed in nasopharyngeal swabs of patients with severe COVID-19 was lately observed by us, pointing towards the potential of miRNAs as possible diagnostic or prognostic biomarkers for predicting outcomes among patients with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection. The objective of the present study was to investigate whether SARS-CoV-2 infection influences the expression levels of messenger RNAs (mRNAs) of key genes involved in miRNA biogenesis. mRNA levels of AGO2, DICER1, DGCR8, DROSHA, and Exportin-5 (XPO5) were measured by quantitative reverse-transcription polymerase chain reaction (RT-qPCR) in nasopharyngeal swab specimens from patients with COVID-19 and controls, as well as in cells infected with SARS-CoV-2 in vitro. Our data showed that the mRNA expression levels of AGO2, DICER1, DGCR8, DROSHA, and XPO5 were not significantly different in patients with severe COVID-19 when compared to patients with non-severe COVID-19 and controls. Similarly, the mRNA expression of these genes was not affected by SARS-CoV-2 infection in NHBE and Calu-3 cells. However, in Vero E6 cells, AGO2, DICER1, DGCR8, and XPO5 mRNA levels were slightly upregulated 24 h after infection with SARS-CoV-2. In conclusion, we did not find evidence for downregulation of mRNA levels of miRNA biogenesis genes during SARS-CoV-2 infection, neither ex vivo nor in vitro. |
format | Online Article Text |
id | pubmed-10222706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102227062023-05-28 Genes Involved in miRNA Biogenesis Are Not Downregulated in SARS-CoV-2 Infection Garnier, Nathalie Sane, Famara Massara, Layal Soncin, Fabrice Gosset, Philippe Hober, Didier Szunerits, Sabine Engelmann, Ilka Viruses Article miRNAs, small non-coding RNAs that regulate gene expression, are involved in various pathological processes, including viral infections. Virus infections may interfere with the miRNA pathway through the inhibition of genes involved in miRNA biogenesis. A reduction in the number and the levels of miRNAs expressed in nasopharyngeal swabs of patients with severe COVID-19 was lately observed by us, pointing towards the potential of miRNAs as possible diagnostic or prognostic biomarkers for predicting outcomes among patients with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection. The objective of the present study was to investigate whether SARS-CoV-2 infection influences the expression levels of messenger RNAs (mRNAs) of key genes involved in miRNA biogenesis. mRNA levels of AGO2, DICER1, DGCR8, DROSHA, and Exportin-5 (XPO5) were measured by quantitative reverse-transcription polymerase chain reaction (RT-qPCR) in nasopharyngeal swab specimens from patients with COVID-19 and controls, as well as in cells infected with SARS-CoV-2 in vitro. Our data showed that the mRNA expression levels of AGO2, DICER1, DGCR8, DROSHA, and XPO5 were not significantly different in patients with severe COVID-19 when compared to patients with non-severe COVID-19 and controls. Similarly, the mRNA expression of these genes was not affected by SARS-CoV-2 infection in NHBE and Calu-3 cells. However, in Vero E6 cells, AGO2, DICER1, DGCR8, and XPO5 mRNA levels were slightly upregulated 24 h after infection with SARS-CoV-2. In conclusion, we did not find evidence for downregulation of mRNA levels of miRNA biogenesis genes during SARS-CoV-2 infection, neither ex vivo nor in vitro. MDPI 2023-05-16 /pmc/articles/PMC10222706/ /pubmed/37243263 http://dx.doi.org/10.3390/v15051177 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Garnier, Nathalie Sane, Famara Massara, Layal Soncin, Fabrice Gosset, Philippe Hober, Didier Szunerits, Sabine Engelmann, Ilka Genes Involved in miRNA Biogenesis Are Not Downregulated in SARS-CoV-2 Infection |
title | Genes Involved in miRNA Biogenesis Are Not Downregulated in SARS-CoV-2 Infection |
title_full | Genes Involved in miRNA Biogenesis Are Not Downregulated in SARS-CoV-2 Infection |
title_fullStr | Genes Involved in miRNA Biogenesis Are Not Downregulated in SARS-CoV-2 Infection |
title_full_unstemmed | Genes Involved in miRNA Biogenesis Are Not Downregulated in SARS-CoV-2 Infection |
title_short | Genes Involved in miRNA Biogenesis Are Not Downregulated in SARS-CoV-2 Infection |
title_sort | genes involved in mirna biogenesis are not downregulated in sars-cov-2 infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10222706/ https://www.ncbi.nlm.nih.gov/pubmed/37243263 http://dx.doi.org/10.3390/v15051177 |
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