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Synchronized Orchestration of miR-99b and let-7g Positively Regulates Rotavirus Infection by Modulating Autophagy

Rotavirus (RV), the major etiological agent of viral gastroenteritis in young children, kills over 200 thousand infants each year. In spite of available vaccines, rotaviral diarrhoea is still a major problem in developing countries of Asia and Africa. Therefore, the studies on RV infection and host...

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Autores principales: Mukhopadhyay, Urbi, Chanda, Shampa, Patra, Upayan, Mukherjee, Arpita, Rana, Santanu, Mukherjee, Anupam, Chawla-Sarkar, Mamta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362297/
https://www.ncbi.nlm.nih.gov/pubmed/30718795
http://dx.doi.org/10.1038/s41598-018-38473-8
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author Mukhopadhyay, Urbi
Chanda, Shampa
Patra, Upayan
Mukherjee, Arpita
Rana, Santanu
Mukherjee, Anupam
Chawla-Sarkar, Mamta
author_facet Mukhopadhyay, Urbi
Chanda, Shampa
Patra, Upayan
Mukherjee, Arpita
Rana, Santanu
Mukherjee, Anupam
Chawla-Sarkar, Mamta
author_sort Mukhopadhyay, Urbi
collection PubMed
description Rotavirus (RV), the major etiological agent of viral gastroenteritis in young children, kills over 200 thousand infants each year. In spite of available vaccines, rotaviral diarrhoea is still a major problem in developing countries of Asia and Africa. Therefore, the studies on RV infection and host antiviral responses are warranted. The active correlation between virus infection and activation of autophagy machinery and positive influence of autophagy on RV replication have been documented recently. Previous study from our group showed dysregulation of several cellular miRNAs during RV infection, though their significance remained largely unknown. Since cellular microRNAs (miRNAs) have been implicated in the control of several fundamental biological processes including stress response and autophagy, we focused on two miRNAs, miR-99b and let-7g, and analyzed their function to gain insight into the miRNA-autophagy crosstalk during RV infection. This study shows that RV suppresses let-7g expression but enhances miR-99b that in turn augment major autophagy regulators. Ectopic expression of let-7g and knockdown of miR-99b resulted in inhibition of autophagy, hence, reduction of RV replication. Overall, our study highlights new mechanistic insights for understanding the role of miRNAs in modulating RV infection and possibility of using RNA interference as an antiviral therapeutic target.
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spelling pubmed-63622972019-02-07 Synchronized Orchestration of miR-99b and let-7g Positively Regulates Rotavirus Infection by Modulating Autophagy Mukhopadhyay, Urbi Chanda, Shampa Patra, Upayan Mukherjee, Arpita Rana, Santanu Mukherjee, Anupam Chawla-Sarkar, Mamta Sci Rep Article Rotavirus (RV), the major etiological agent of viral gastroenteritis in young children, kills over 200 thousand infants each year. In spite of available vaccines, rotaviral diarrhoea is still a major problem in developing countries of Asia and Africa. Therefore, the studies on RV infection and host antiviral responses are warranted. The active correlation between virus infection and activation of autophagy machinery and positive influence of autophagy on RV replication have been documented recently. Previous study from our group showed dysregulation of several cellular miRNAs during RV infection, though their significance remained largely unknown. Since cellular microRNAs (miRNAs) have been implicated in the control of several fundamental biological processes including stress response and autophagy, we focused on two miRNAs, miR-99b and let-7g, and analyzed their function to gain insight into the miRNA-autophagy crosstalk during RV infection. This study shows that RV suppresses let-7g expression but enhances miR-99b that in turn augment major autophagy regulators. Ectopic expression of let-7g and knockdown of miR-99b resulted in inhibition of autophagy, hence, reduction of RV replication. Overall, our study highlights new mechanistic insights for understanding the role of miRNAs in modulating RV infection and possibility of using RNA interference as an antiviral therapeutic target. Nature Publishing Group UK 2019-02-04 /pmc/articles/PMC6362297/ /pubmed/30718795 http://dx.doi.org/10.1038/s41598-018-38473-8 Text en © The Author(s) 2019 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
Mukhopadhyay, Urbi
Chanda, Shampa
Patra, Upayan
Mukherjee, Arpita
Rana, Santanu
Mukherjee, Anupam
Chawla-Sarkar, Mamta
Synchronized Orchestration of miR-99b and let-7g Positively Regulates Rotavirus Infection by Modulating Autophagy
title Synchronized Orchestration of miR-99b and let-7g Positively Regulates Rotavirus Infection by Modulating Autophagy
title_full Synchronized Orchestration of miR-99b and let-7g Positively Regulates Rotavirus Infection by Modulating Autophagy
title_fullStr Synchronized Orchestration of miR-99b and let-7g Positively Regulates Rotavirus Infection by Modulating Autophagy
title_full_unstemmed Synchronized Orchestration of miR-99b and let-7g Positively Regulates Rotavirus Infection by Modulating Autophagy
title_short Synchronized Orchestration of miR-99b and let-7g Positively Regulates Rotavirus Infection by Modulating Autophagy
title_sort synchronized orchestration of mir-99b and let-7g positively regulates rotavirus infection by modulating autophagy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362297/
https://www.ncbi.nlm.nih.gov/pubmed/30718795
http://dx.doi.org/10.1038/s41598-018-38473-8
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