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Oligonucleotide-Based Approaches to Inhibit Dengue Virus Replication

Dengue fever is one of the most common viral infections affecting humans. It is an expanding public health problem, particularly in tropical and subtropical regions. No effective vaccine or antiviral therapies against Dengue virus (DENV) infection are available. Therefore, there is a strong need to...

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Autores principales: Panda, Kingshuk, Alagarasu, Kalichamy, Parashar, Deepti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918374/
https://www.ncbi.nlm.nih.gov/pubmed/33670247
http://dx.doi.org/10.3390/molecules26040956
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author Panda, Kingshuk
Alagarasu, Kalichamy
Parashar, Deepti
author_facet Panda, Kingshuk
Alagarasu, Kalichamy
Parashar, Deepti
author_sort Panda, Kingshuk
collection PubMed
description Dengue fever is one of the most common viral infections affecting humans. It is an expanding public health problem, particularly in tropical and subtropical regions. No effective vaccine or antiviral therapies against Dengue virus (DENV) infection are available. Therefore, there is a strong need to develop safe and effective therapeutic strategies that can reduce the burden and duration of hospitalizations due to this life-threatening disease. Oligonucleotide-based strategies are considered as an attractive means of inhibiting viral replication since oligonucleotides can be designed to interact with any viral RNA, provided its sequence is known. The resultant targeted destruction of viral RNA interferes with viral replication without inducing any adverse effects on cellular processes. In this review, we elaborate the ribozymes, RNA interference, CRISPR, aptamer and morpholino strategies for the inhibition of DENV replication and discuss the challenges involved in utilizing such approaches.
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spelling pubmed-79183742021-03-02 Oligonucleotide-Based Approaches to Inhibit Dengue Virus Replication Panda, Kingshuk Alagarasu, Kalichamy Parashar, Deepti Molecules Review Dengue fever is one of the most common viral infections affecting humans. It is an expanding public health problem, particularly in tropical and subtropical regions. No effective vaccine or antiviral therapies against Dengue virus (DENV) infection are available. Therefore, there is a strong need to develop safe and effective therapeutic strategies that can reduce the burden and duration of hospitalizations due to this life-threatening disease. Oligonucleotide-based strategies are considered as an attractive means of inhibiting viral replication since oligonucleotides can be designed to interact with any viral RNA, provided its sequence is known. The resultant targeted destruction of viral RNA interferes with viral replication without inducing any adverse effects on cellular processes. In this review, we elaborate the ribozymes, RNA interference, CRISPR, aptamer and morpholino strategies for the inhibition of DENV replication and discuss the challenges involved in utilizing such approaches. MDPI 2021-02-11 /pmc/articles/PMC7918374/ /pubmed/33670247 http://dx.doi.org/10.3390/molecules26040956 Text en © 2021 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
Panda, Kingshuk
Alagarasu, Kalichamy
Parashar, Deepti
Oligonucleotide-Based Approaches to Inhibit Dengue Virus Replication
title Oligonucleotide-Based Approaches to Inhibit Dengue Virus Replication
title_full Oligonucleotide-Based Approaches to Inhibit Dengue Virus Replication
title_fullStr Oligonucleotide-Based Approaches to Inhibit Dengue Virus Replication
title_full_unstemmed Oligonucleotide-Based Approaches to Inhibit Dengue Virus Replication
title_short Oligonucleotide-Based Approaches to Inhibit Dengue Virus Replication
title_sort oligonucleotide-based approaches to inhibit dengue virus replication
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918374/
https://www.ncbi.nlm.nih.gov/pubmed/33670247
http://dx.doi.org/10.3390/molecules26040956
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