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Comprehensive computational analysis reveals H5N1 influenza virus-encoded miRNAs and host-specific targets associated with antiviral immune responses and protein binding

H5N1 virus (H5N1V) is highly contagious among birds and it was first detected in humans in 1997 during a poultry outbreak in Hong Kong. As the mechanism of its pathogenesis inside the host is still lacking, in this in-silico study we hypothesized that H5N1V might create miRNAs, which could target th...

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Autores principales: Noor, Fatima, Saleem, Muhammad Hamzah, Javed, Muhammad Rizwan, Chen, Jen-Tsung, Ashfaq, Usman Ali, Okla, Mohammad K., Abdel-Maksoud, Mostafa A., Alwasel, Yasmeen A., Al-Qahtani, Wahidah H., Alshaya, Huda, Yasin, Ghulam, Aslam, Sidra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9084522/
https://www.ncbi.nlm.nih.gov/pubmed/35533150
http://dx.doi.org/10.1371/journal.pone.0263901
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author Noor, Fatima
Saleem, Muhammad Hamzah
Javed, Muhammad Rizwan
Chen, Jen-Tsung
Ashfaq, Usman Ali
Okla, Mohammad K.
Abdel-Maksoud, Mostafa A.
Alwasel, Yasmeen A.
Al-Qahtani, Wahidah H.
Alshaya, Huda
Yasin, Ghulam
Aslam, Sidra
author_facet Noor, Fatima
Saleem, Muhammad Hamzah
Javed, Muhammad Rizwan
Chen, Jen-Tsung
Ashfaq, Usman Ali
Okla, Mohammad K.
Abdel-Maksoud, Mostafa A.
Alwasel, Yasmeen A.
Al-Qahtani, Wahidah H.
Alshaya, Huda
Yasin, Ghulam
Aslam, Sidra
author_sort Noor, Fatima
collection PubMed
description H5N1 virus (H5N1V) is highly contagious among birds and it was first detected in humans in 1997 during a poultry outbreak in Hong Kong. As the mechanism of its pathogenesis inside the host is still lacking, in this in-silico study we hypothesized that H5N1V might create miRNAs, which could target the genes associated with host cellular regulatory pathways, thus provide persistent refuge to the virus. Using bioinformatics approaches, several H5N1V produced putative miRNAs as well as the host genes targeted by these miRNAs were found. Functional enrichment analysis of targeted genes revealed their involvement in many biological pathways that facilitate their host pathogenesis. Eventually, the microarray dataset (GSE28166) was analyzed to validate the altered expression level of target genes and found the genes involved in protein binding and adaptive immune responses. This study presents novel miRNAs and their targeted genes, which upon experimental validation could facilitate in developing new therapeutics against H5N1V infection.
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spelling pubmed-90845222022-05-10 Comprehensive computational analysis reveals H5N1 influenza virus-encoded miRNAs and host-specific targets associated with antiviral immune responses and protein binding Noor, Fatima Saleem, Muhammad Hamzah Javed, Muhammad Rizwan Chen, Jen-Tsung Ashfaq, Usman Ali Okla, Mohammad K. Abdel-Maksoud, Mostafa A. Alwasel, Yasmeen A. Al-Qahtani, Wahidah H. Alshaya, Huda Yasin, Ghulam Aslam, Sidra PLoS One Research Article H5N1 virus (H5N1V) is highly contagious among birds and it was first detected in humans in 1997 during a poultry outbreak in Hong Kong. As the mechanism of its pathogenesis inside the host is still lacking, in this in-silico study we hypothesized that H5N1V might create miRNAs, which could target the genes associated with host cellular regulatory pathways, thus provide persistent refuge to the virus. Using bioinformatics approaches, several H5N1V produced putative miRNAs as well as the host genes targeted by these miRNAs were found. Functional enrichment analysis of targeted genes revealed their involvement in many biological pathways that facilitate their host pathogenesis. Eventually, the microarray dataset (GSE28166) was analyzed to validate the altered expression level of target genes and found the genes involved in protein binding and adaptive immune responses. This study presents novel miRNAs and their targeted genes, which upon experimental validation could facilitate in developing new therapeutics against H5N1V infection. Public Library of Science 2022-05-09 /pmc/articles/PMC9084522/ /pubmed/35533150 http://dx.doi.org/10.1371/journal.pone.0263901 Text en © 2022 Noor et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Noor, Fatima
Saleem, Muhammad Hamzah
Javed, Muhammad Rizwan
Chen, Jen-Tsung
Ashfaq, Usman Ali
Okla, Mohammad K.
Abdel-Maksoud, Mostafa A.
Alwasel, Yasmeen A.
Al-Qahtani, Wahidah H.
Alshaya, Huda
Yasin, Ghulam
Aslam, Sidra
Comprehensive computational analysis reveals H5N1 influenza virus-encoded miRNAs and host-specific targets associated with antiviral immune responses and protein binding
title Comprehensive computational analysis reveals H5N1 influenza virus-encoded miRNAs and host-specific targets associated with antiviral immune responses and protein binding
title_full Comprehensive computational analysis reveals H5N1 influenza virus-encoded miRNAs and host-specific targets associated with antiviral immune responses and protein binding
title_fullStr Comprehensive computational analysis reveals H5N1 influenza virus-encoded miRNAs and host-specific targets associated with antiviral immune responses and protein binding
title_full_unstemmed Comprehensive computational analysis reveals H5N1 influenza virus-encoded miRNAs and host-specific targets associated with antiviral immune responses and protein binding
title_short Comprehensive computational analysis reveals H5N1 influenza virus-encoded miRNAs and host-specific targets associated with antiviral immune responses and protein binding
title_sort comprehensive computational analysis reveals h5n1 influenza virus-encoded mirnas and host-specific targets associated with antiviral immune responses and protein binding
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9084522/
https://www.ncbi.nlm.nih.gov/pubmed/35533150
http://dx.doi.org/10.1371/journal.pone.0263901
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