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Role of microRNA and Oxidative Stress in Influenza A Virus Pathogenesis

MicroRNAs (miRNAs) are non-coding RNAs that regulate diverse cellular pathways by controlling gene expression. Increasing evidence has revealed their critical involvement in influenza A virus (IAV) pathogenesis. Host–IAV interactions induce different levels of oxidative stress (OS) by disrupting the...

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Autores principales: Haque, Md Mamunul, Murale, Dhiraj P., Lee, Jun-Seok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728370/
https://www.ncbi.nlm.nih.gov/pubmed/33255826
http://dx.doi.org/10.3390/ijms21238962
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author Haque, Md Mamunul
Murale, Dhiraj P.
Lee, Jun-Seok
author_facet Haque, Md Mamunul
Murale, Dhiraj P.
Lee, Jun-Seok
author_sort Haque, Md Mamunul
collection PubMed
description MicroRNAs (miRNAs) are non-coding RNAs that regulate diverse cellular pathways by controlling gene expression. Increasing evidence has revealed their critical involvement in influenza A virus (IAV) pathogenesis. Host–IAV interactions induce different levels of oxidative stress (OS) by disrupting the balance between reactive oxygen species (ROS) and antioxidant factors. It is thought that miRNA may regulate the expression of ROS; conversely, ROS can induce or suppress miRNA expression during IAV infection. Thus, miRNA and OS are the two key factors of IAV infection and pathogenesis. Accordingly, interactions between OS and miRNA during IAV infection might be a critical area for further research. In this review, we discuss the crosstalk between miRNAs and OS during IAV infection. Additionally, we highlight the potential of miRNAs as diagnostic markers and therapeutic targets for IAV infections. This knowledge will help us to study host–virus interactions with novel intervention strategies.
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spelling pubmed-77283702020-12-11 Role of microRNA and Oxidative Stress in Influenza A Virus Pathogenesis Haque, Md Mamunul Murale, Dhiraj P. Lee, Jun-Seok Int J Mol Sci Review MicroRNAs (miRNAs) are non-coding RNAs that regulate diverse cellular pathways by controlling gene expression. Increasing evidence has revealed their critical involvement in influenza A virus (IAV) pathogenesis. Host–IAV interactions induce different levels of oxidative stress (OS) by disrupting the balance between reactive oxygen species (ROS) and antioxidant factors. It is thought that miRNA may regulate the expression of ROS; conversely, ROS can induce or suppress miRNA expression during IAV infection. Thus, miRNA and OS are the two key factors of IAV infection and pathogenesis. Accordingly, interactions between OS and miRNA during IAV infection might be a critical area for further research. In this review, we discuss the crosstalk between miRNAs and OS during IAV infection. Additionally, we highlight the potential of miRNAs as diagnostic markers and therapeutic targets for IAV infections. This knowledge will help us to study host–virus interactions with novel intervention strategies. MDPI 2020-11-25 /pmc/articles/PMC7728370/ /pubmed/33255826 http://dx.doi.org/10.3390/ijms21238962 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Haque, Md Mamunul
Murale, Dhiraj P.
Lee, Jun-Seok
Role of microRNA and Oxidative Stress in Influenza A Virus Pathogenesis
title Role of microRNA and Oxidative Stress in Influenza A Virus Pathogenesis
title_full Role of microRNA and Oxidative Stress in Influenza A Virus Pathogenesis
title_fullStr Role of microRNA and Oxidative Stress in Influenza A Virus Pathogenesis
title_full_unstemmed Role of microRNA and Oxidative Stress in Influenza A Virus Pathogenesis
title_short Role of microRNA and Oxidative Stress in Influenza A Virus Pathogenesis
title_sort role of microrna and oxidative stress in influenza a virus pathogenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728370/
https://www.ncbi.nlm.nih.gov/pubmed/33255826
http://dx.doi.org/10.3390/ijms21238962
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